Key words
piperizinones - cyclization reactions - allenes - nucleophilic substitution - combinatorial synthesis
Unique properties of small heterocyclic motifs have made them pivotal participants in drug discovery processes.[1]
[2]
[3]
[4]
[5] Their structural varieties provide opportunities to finely balance features of biologically active compounds as they can play various roles.[6–10] Small heterocyclic rings are used as drug scaffold, bioisosteric replacement or they control specific physicochemical/pharmacokinetic or prodrug properties. Needless to mention, heterocyclic cores are frequently a constitutional part of many natural products as well.[11,12]
Amongst the heterocyclic skeletons, piperazinones are considered to be a privileged structure in medicinal chemistry.[13]
[14] It is a structural part of many drugs and natural products (Figure [1])[15–18] but its particular value is associated with peptidomimetic properties resulting from the specific positioning of the heteroatoms.[19]
[20] Significance of piperazinone motif, perhaps primarily in medicinal chemistry, prompted development of various synthetic methodologies for its preparation.[21]
[22]
Figure 1 Selected piperazinone derivatives
Amongst them, particularly interesting are those allowing formation of two bonds in one step as they usually provide facile access to structural diversity while simplifying the synthetic process. These methodologies are widely explored and strategically many of them were developed.[21] A highly efficient formation of piperazinones outlined in Scheme [1] is based on the simultaneous formation of C(3)–N(4) and N(4)–C(5) bonds and it relies on the nucleophilicity of the amino component employed as the source of N(4). The reported methodologies of this type combine primary amines and typical electrophiles, alkyl halides and aldehyde/ketones (Scheme [1], approach a) or alkyl halides and electron-deficient conjugated double bonds (Scheme [1], approach b).[23]
[24] Both processes are very efficient producing piperazinones in high yields. As an alternative to these methods, we developed a related transformation combining electrophilic alkyl halide and allene as a masked electrophile in reaction promoted by Ag(I)/Pd(II) catalysis (Scheme [1], approach c). Interestingly, related process for the formation of the 5-membered ring was reported by the Broggini group but was never explored for the formation of the 6-membered ring.[25] In addition, the synthesis of the 5-membered ring was carried out intramolecularly with the preformed amine whereas our transformation utilized alkyl chlorides, which was in situ transformed to a nucleophilic secondary amino functionality. The use of aryl iodide to transform allene into the electrophilic moiety ensures additional point of diversity.
Scheme 1 Synthesis of piperazinones via C(3)–N(4) and N(4)–C(5) bonds formation
Table 1 Optimization of the Reaction Conditions for the Synthesis of Piperazinonesa
|
|
Entry
|
[Pd]
|
[Ag]
|
BnNH2
|
Base
|
Solvent
|
Yield (%)b
|
|
a
|
Pd(PPh3)4
|
–
|
3
|
Cs2CO3
|
CH3CN
|
43
|
|
b
|
Pd(PPh3)4
|
AgNO3
|
3
|
Cs2CO3
|
CH3CN
|
58
|
|
c
|
Pd(PPh3)4
|
Ag2CO3
|
3
|
Cs2CO3
|
CH3CN
|
8
|
|
d
|
Pd(PPh3)4
|
AgOAc
|
3
|
Cs2CO3
|
CH3CN
|
18
|
|
e
|
Pd(PPh3)4
|
AgOTf
|
3
|
Cs2CO3
|
CH3CN
|
53
|
|
f
|
Pd(OAc)2/PPh3 (0.1/0.2 equiv)
|
AgNO3
|
3
|
Cs2CO3
|
CH3CN
|
23
|
|
g
|
Pd(dba)2/PPh3 (0.1/0.2 equiv)
|
AgNO3
|
3
|
Cs2CO3
|
CH3CN
|
45
|
|
h
|
Pd(OAc)2/XantPhos (0.1/0.1 equiv)
|
AgNO3
|
3
|
Cs2CO3
|
CH3CN
|
28
|
|
i
|
Pd(PPh3)4
|
AgNO3
|
3
|
Et3N
|
CH3CN
|
7
|
|
k
|
Pd(PPh3)4
|
AgNO3
|
3
|
Cs2CO3
|
DMF
|
3
|
|
l
|
Pd(PPh3)4
|
AgNO3 (0.2 equiv)
|
3
|
Cs2CO3
|
CH3CN
|
71
|
|
m
|
Pd(PPh3)4
|
AgNO3 (0.5 equiv)
|
3
|
Cs2CO3
|
CH3CN
|
74 (63)
|
|
n
|
Pd(PPh3)4
|
AgNO3 (2.2 equiv)
|
3
|
Cs2CO3
|
CH3CN
|
51
|
|
o
|
Pd(PPh3)4
|
AgNO3 (1 equiv)
|
5
|
Cs2CO3
|
CH3CN
|
77
|
|
p
|
Pd(PPh3)4
|
AgNO3 (1 equiv)
|
1.5
|
Cs2CO3
|
CH3CN
|
27
|
|
q
|
Pd(PPh3)4
|
AgNO3 (0.5 equiv)
|
5
|
Cs2CO3
|
CH3CN
|
77
|
|
r
|
Pd(dba)2/PPh3
(0.1/0.2 equiv)
|
AgNO3 (0.5 equiv)
|
3
|
Cs2CO3
|
CH3CN
|
72 (62)
|
a Reaction conditions: 1 (0.1 mmol), ), p-MeOC6H4I (0.12 mmol), BnNH2 (0.3 mmol) Ag-salt (0.1 mmol), base (0.3 mmol), Pd/ligand source (0.01 mmol), solvent (5 mL), 85–90 °C, 16 h, unless otherwise indicated.
b Yield calculated from NMR data using pyridine as an internal standard and, in parentheses, isolated yield after column chromatography
Our first experiment (Table [1], entry a) was performed with chloride 1 using benzylamine in excess, aryl iodide, Pd(PPh3)4, and Cs2CO3 as base in MeCN as solvent. Analysis of the 1H NMR spectrum of the crude reaction mixture suggested formation of the expected piperazinone 2 in 43% yield. As the yield was not synthetically fully satisfactory, we next performed the same reaction with the addition of AgNO3 (entry b) anticipating that it might facilitate the nucleophilic displacement of the chloride. Indeed, the reaction yield increased to 58% and the result prompted surveying few additional Ag-salts (entries c–e). While Ag2CO3 and AgOAc proved to be inefficient, AgOTf afforded the expected piperazinone 2 in a yield comparable to that obtained with AgNO3. As AgOTf is more expensive and hygroscopic, we continued our study with AgNO3 and further explored several Pd-catalytic systems (entries f–h). Varying Pd-source and the phosphine ligand did not improve the reaction outcome. Two following experiments demonstrated essential role of base and solvent. Namely, performing the reaction in DMF (entry k) or using Et3N as base (entry i) had detrimental effect on the reaction yield. We finally explored the influence of stoichiometry of AgNO3 and amine. Decreasing the quantities of Ag-salt to 0.2 or 0.5 equivalent improved the yields to 71% and 74% respectively (entries l, m). A similar effect was observed when Pd(dba)2/PPh3 was used as the catalytic system in conjunction with 0.5 equivalent of AgNO3 (entry r). Further slight improvement was the consequence of increasing the amount of amine (entries o, q) while completely opposite effect was triggered by reducing the amine quantities (entry p).
Having optimized the reaction conditions, we then explored the scope of the synthetic route (Scheme [2]). Under the above described settings various aryl iodides possessing both electron-donating and electron-accepting groups efficiently participated in the reaction process affording product 3a–e in good yields. A single example of the aryl iodide having o-substituent produced 3c in 57% yield demonstrating tolerance of the reacting functionality to the proximal sterically more demanding substituent. Comparable results were obtained in the reactions with various amines. All aliphatic amines with no other functionalities in the side chain afforded products 3g, 3h, and 3i in high yields. Similar results were obtained with amines having relatively inert distal ester groups (3n, 3p). The conditions also tolerated several acidic functionalities such as OH, NHBoc or indole-NH yielding the products 3j, 3k, 3m, 3o, 3q in synthetically acceptable manners. Further to this, chelating aminopyridine derivative employed for the preparation of 3l did not obstruct the process although two metal species were present in the reaction medium. Finally, double bond was also tolerated suggesting a significantly different rate of the reactions of arylpalladium intermediate with allene or alkene. To demonstrate synthetic utility of the above process, the selected reactions were performed at 1 mmol scale under the otherwise same conditions. Product 3f was isolated after chromatographic purification in 64% yield (compared to 66% at 0.1 mmol scale) while 3q was isolated in 59% (compared to 50% at 0.1 mmol scale).
Scheme 2 Scope of the reaction. Reagents and conditions: 1 (0.1 mmol), ), ArI (0.12 mmol), RNH2 (0.3 mmol), AgNO3(0.05 mmol), Cs2CO3 (0.3 mmol), Pd(PPh3)4 (0.01mmol), CH3CN (5 mL), 85–90 °C, 16 h.
Scheme 3 Combinatorial synthesis of piperazinone derivatives
The described process introduces two diversity points into the piperazinone products represented by the amino and the iodo components. Therefore, we briefly explored the combinatorial approach for their preparation (Scheme [3] A–C). The reaction outlined in Scheme [3]A was performed under the above described conditions using benzylamine and three iodides to afford the expected 3j, 3a, and 3b as a mixture in 56% yield and in 3:3:1 ratio, respectively. Similar efficiency was demonstrated by the reaction employing three different amines (Scheme [3]B). The products 3a, 3i, and 3g were obtained in 56% yield and in 1.8:1:1.2 ratio, respectively. Finally, we performed the reaction with different amines and aryl iodides to obtain a clean mixture of four products 3a, 3g, 3d, and 4 (74% yield,1.8:3.2:1:1.4 ratio, respectively) (Scheme [3]C). The experiments outlined in Scheme [3] demonstrated simplicity and efficiency of the described methodology for the potential combinatorial synthesis of piperazinones.
The depicted cascade transformation combines several processes with compatible reaction rate ideally ordered to yield piperazinone derivatives in good yields. The reaction is likely to start with displacement of chloride in starting allene SM (Scheme [4]A) with primary amine creating derivative a (Scheme [4]A) possessing nucleophilic secondary amino group.
Scheme 4 Mechanistic consideration
The parallel oxidative addition of the Pd(0) onto the ArI generates an intermediate that reacts with allene moiety creating π-allyl Pd b (Scheme [4]A). The final step is the well-established nucleophilic substitution involving proximal secondary amine and π-allyl Pd intermediate to create product P (Scheme [4]A). Alternative pathways which would incorporate initial formation of π-allyl Pd c followed by reaction with primary amine to form d or e and then the cyclized product f or P, as outlined in Scheme [4]A, are unlikely to be effective. Such routes would involve either the reaction of nucleophilic amine with sterically more demanding internal position of π-allyl Pd c to form d or formation of 8-membered ring product f (Scheme [4]A). Monitoring of the reaction by 1H NMR did not reveal any product/by-product that would result from the alternative pathways. In addition, the reaction performed with substrate 5 produced highly regioselectively amine 6 in 78% yield as the product of nucleophilic attack from the less hindered side of the π-allyl Pd-intermediate (Scheme [4]B). This result supported nucleophilic displacement of chloride as the first step in the reaction cascade. Our experimental protocol employs an excess of the primary amine nucleophile. However, we did not observe any by-product resulting from the intermolecular reaction of b with amine, such as g or h, (same products would be obtained by reaction of d/e with amine), demonstrating the efficiency of the ring closure process.
An efficient cascade process employing chloroallenyl amides for the preparation of piperazinone derivatives was developed. In situ formation of the nucleophilic secondary amine and following nucleophilic displacement onto the proximal π-allyl Pd motif afforded the target compounds in yields typically ~50–90%. Structural variations are easily introduced by appropriate selection of reacting components thus making this transformation well suited for combinatorial synthesis of piperizinone derivatives.
IR spectra were recorded on an IR Thermo Scientific NICOLET iS10 (4950) spectrophotometer. 1H and 13C NMR spectra were recorded on a Bruker Ascend 400 (400 MHz) spectrometer. CDCl3 was used as a solvent, and chemical shifts are given in parts per million (δ) downfield from TMS as the internal standard. Mass spectral data were recorded using an LTQ Orbitrap XL. Flash chromatography employed silica gel 60 (230–400 mesh), while TLC was carried out using alumina plates with a 0.25 mm silica layer (Kieselgel 60 F254; Merck). Compounds were visualized by staining with KMnO4 solution. The starting compound N-2,3-butadien-1-ylbenzenemethanamine was synthesized following the literature procedure.[26]
N-Benzyl-N-buta-2,3-dienyl-2-chloroacetamide (1)
N-Benzyl-N-buta-2,3-dienyl-2-chloroacetamide (1)
N-2,3-Butadien-1-ylbenzenemethanamine (4 mmol, 636 mg, 1 equiv) was added to a flame-dried flask under N2 pressure containing anhyd DCM (10 mL) and Et3N (8 mmol, 1.11 mL, 2 equiv). Then, chloroacetyl chloride (4.8 mmol, 0.38 mL, 1.2 equiv) was added dropwise to the stirred solution at 0 °C. The solution was stirred for 1 h at 0 °C and then poured into a separatory funnel containing aq 2 M HCl (10 mL). The aqueous layer was extracted with DCM. The organic layers were collected, washed with brine, dried (anhyd Na2SO4) and concentrated in vacuo. The crude oil was purified by silica gel flash chromatography (SiO2, 1:1 v/v PE– Et2O) to give a thick orange oil; yield: 735 mg (78%).
IR (ATR): 2927, 1651, 1422, 1139, 850, 698 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.50–7.04 (m, 5 H, both rotamers), 5.21–5.04 (m, 1 H, both rotamers), 4.88 (dt, J = 6.3, 3.0 Hz, 2 H, major), 4.83–4.75 (m, 2 H, minor), 4.62 (s, 2 H, both rotamers), 4.16 (s, 2 H, major), 4.07 (s, 2 H, minor), 4.05–3.96 (m, 2 H, minor), 3.92–3.84 (m, 2 H, major).
13C NMR (101 MHz, CDCl3): δ = 209.3, 208.5, 166.9, 166.8, 136.6, 135.8, 129.0, 128.7, 128.3, 127.9, 127.6, 126.6, 86.6, 85.6, 78.1, 76.7, 50.7, 48.81, 45.5, 44.7, 41.3, 41.2.
HRMS (ESI): m/z calcd for [C13H14ClNO + Na]+: 258.06561; found: 258.06528.
Synthesis of Piperazinones; General Procedure
Synthesis of Piperazinones; General Procedure
A mixture of 1 (0.1 mmol), ArI (0.12 mmol), RNH2 (0.3 mmol), AgNO3 (0.05 mmol), Cs2CO3 (0.3 mmol), and Pd(PPh3)4 (0.01 mmol) in CH3CN (5 mL) was heated in a N2 atmosphere at reflux for 16 h. After completion of the reaction, the mixture was cooled to rt, and the solvent was removed under reduced pressure. The crude mixture was purified by flash chromatography to afford the product.
Combinatorial Synthesis of Piperazinones; General Procedures (Scheme [3])
Combinatorial Synthesis of Piperazinones; General Procedures (Scheme [3])
A: A mixture of 1 (0.2 mmol), three aryl iodides (0.08 mmol each), benzylamine (0.6 mmol) AgNO3 (0.1 mmol), Cs2CO3 (0.6 mmol), and Pd(PPh3)4 (0.02 mmol) in CH3CN (10 mL) was heated in a N2 atmosphere at reflux for 16 h. After completion of the reaction, the mixture was cooled to rt, and the solvent was removed under reduced pressure. The crude mixture was purified by flash chromatography to afford the products 3j,a,b.
B: A mixture of 1 (0.2 mmol), 2-iodonaphthalene (0.24 mmol), three amines (0.2 mmol each), AgNO3 (0.1 mmol), Cs2CO3 (0.6 mmol), and Pd(PPh3)4 (0.02 mmol) in CH3CN (10 mL) was heated in a N2 atmosphere at reflux for 16 h. After completion of the reaction, the mixture was cooled to rt, and the solvent was removed under reduced pressure. The crude mixture was purified by flash chromatography to afford the products 3a,i,g.
C: A mixture of 1 (0.2 mmol), two aryl iodides (0.12 mmol each), two amines (0.3 mmol each), AgNO3 (0.1 mmol), Cs2CO3 (0.6 mmol), and Pd(PPh3)4 (0.02 mmol) in CH3CN (10 ml) was heated in a N2 atmosphere at reflux for 16 h. After completion of the reaction, the mixture was cooled to rt, and the solvent was removed under reduced pressure. The crude mixture was purified by flash chromatography to afford the products 3a,g,d,4.
1,4-Dibenzyl-5-[1-(4-methoxyphenyl)vinyl]piperazin-2-one (2)
1,4-Dibenzyl-5-[1-(4-methoxyphenyl)vinyl]piperazin-2-one (2)
Compound 2 was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (26.1 mg, 63%) as an orange oil.
IR (ATR): 3028, 1651, 1510, 1246, 698 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.50 (d, J = 8.6 Hz, 2 H), 7.33–7.20 (m, 10 H), 6.87 (d, J = 8.6 Hz, 2 H), 5.50 (s, 1 H), 5.33 (s, 1 H), 4.80 (d, J = 14.7 Hz, 1 H), 4.33 (d, J = 14.6 Hz, 1 H), 4.13 (d, J = 12.9 Hz, 1 H), 3.82 (s, 3 H), 3.63 (dd, J = 9.7, 4.1 Hz, 1 H), 3.55 (d, J = 17.0 Hz, 1 H), 3.50–3.39 (m, 1 H), 3.22 (dd, J = 12.2, 4.1 Hz, 1 H), 3.10 (d, J = 12.9 Hz, 1 H), 2.97 (d, J = 17.0 Hz, 1 H).
13C NMR (101 MHz, CDCl3): δ = 167.3, 159.6, 144.9, 137.5, 136.5, 131.8, 128.9, 128.7, 128.4, 128.2, 127.9, 127.6, 127.3, 116.3, 113.8, 64.0, 58.2, 55.7, 55.3, 50.2, 49.4.
HRMS (ESI): m/z calcd for [C27H28N2O2 + H]+: 413.22235; found: 413.22139.
1,4-Dibenzyl-5-(1-naphthalen-2-ylvinyl)piperazin-2-one (3a)
1,4-Dibenzyl-5-(1-naphthalen-2-ylvinyl)piperazin-2-one (3a)
Compound 3a was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (35.1 mg, 81%) as an orange oil.
IR (ATR): 3028, 2922, 1651, 1128, 752, 697 cm–1.
1H NMR (400 MHz, CDCl3): δ = 8.04 (s, 1 H), 7.82 (dd, J = 9.3, 5.5 Hz, 3 H), 7.61 (dd, J = 8.6, 1.4 Hz, 1 H), 7.49 (dd, J = 6.4, 3.1 Hz, 2 H), 7.28 (dt, J = 6.3, 5.5 Hz, 10 H), 5.71 (s, 1 H), 5.51 (s, 1 H), 4.81 (d, J = 14.7 Hz, 1 H), 4.34 (d, J = 14.7 Hz, 1 H), 4.21 (d, J = 12.9 Hz, 1 H), 3.79 (dd, J = 9.4, 4.2 Hz, 1 H), 3.62 (d, J = 17.1 Hz, 1 H), 3.51 (dd, J = 12.1, 9.5 Hz, 1 H), 3.30 (dd, J = 12.2, 4.2 Hz, 1 H), 3.19 (d, J = 13.0 Hz, 1 H), 3.03 (d, J = 17.0 Hz, 1 H).
13C NMR (101 MHz, CDCl3): δ = 167.3, 145.5, 137.4, 136.7, 136.49, 133.2, 133.0, 128.9, 128.7, 128.4, 128.3, 128.2, 128.1, 127.6, 127.6, 127.4, 126.4, 126.3, 125.7, 124.9, 118.3, 63.7, 58.4, 55.7, 50.1, 49.4.
HRMS (ESI): m/z calcd for [C30H28N2O + H]+: 433.22744; found: 433.22665.
1,4-Dibenzyl-5-[1-(4-fluorophenyl)vinyl]piperazin-2-one (3b)
1,4-Dibenzyl-5-[1-(4-fluorophenyl)vinyl]piperazin-2-one (3b)
Compound 3b was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (27.6 mg, 69%) as an orange oil.
IR (ATR): 2921, 1651, 1507, 1226, 840, 698 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.49 (dd, J = 8.4, 5.5 Hz, 2 H), 7.36–7.18 (m, 10 H), 7.01 (t, J = 8.6 Hz, 2 H), 5.51 (s, 1 H), 5.37 (s, 1 H), 4.77 (d, J = 14.6 Hz, 1 H), 4.36 (d, J = 14.6 Hz, 1 H), 4.07 (d, J = 13.0 Hz, 1 H), 3.64–3.68 (m, 1 H), 3.54 (d, J = 17.1 Hz, 1 H), 3.47–3.38 (m, 1 H), 3.24 (dd, J = 12.2, 4.2 Hz, 1 H), 3.15 (d, J = 13.0 Hz, 1 H), 3.00 (d, J = 17.1 Hz, 1 H).
13C NMR (101 MHz, CDCl3): δ = 167.2, 162.6 (J
C,F = 246 Hz), 144.7, 137.3, 136.4, 135.4, 135.4, 128.8, 128.7, 128.6, 128.5, 128.5, 128.2, 127.6, 127.4, 117.7, 115.4, 115.2, 63.5, 58.0, 55.4, 49.6, 49.4.
HRMS (ESI): m/z calcd for [C26H25FN2O + H]+: 401.20237; found: 401.20150.
1,4-Dibenzyl-5-[1-(2-methoxyphenyl)vinyl]piperazin-2-one (3c)
1,4-Dibenzyl-5-[1-(2-methoxyphenyl)vinyl]piperazin-2-one (3c)
Compound 3c was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (23.4 mg, 57%) as light brown, amorphous solid; mp 46–51 °C.
IR (ATR): 2912, 1640, 1492, 1245, 744, 700 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.34–7.21 (m, 9 H), 7.18 (d, J = 7.2 Hz, 2 H), 7.11 (dd, J = 7.3, 1.1 Hz, 1 H), 6.91 (t, J = 7.4 Hz, 1 H), 6.82 (d, J = 8.3 Hz, 1 H), 5.54 (s, 1 H), 5.37 (s, 1 H), 4.82 (d, J = 14.5 Hz, 1 H), 4.35 (d, J = 14.6 Hz, 1 H), 4.19 (d, J = 13.1 Hz, 1 H), 3.68 (dd, J = 8.5, 3.8 Hz, 1 H), 3.55 (s, 3 H), 3.54–3.47 (m, 2 H), 3.36 (dd, J = 12.0, 8.7 Hz, 1 H), 3.04 (dd, J = 24.5, 15.2 Hz, 2 H).
13C NMR (101 MHz, CDCl3): δ = 167.6, 156.5, 146.6, 138.3, 136.8, 131.3, 130.2, 129.1, 128.7, 128.6, 128.4, 128.3, 127.5, 127.1, 120.8, 117.9, 110.6, 61.2, 57.8, 55.5, 54.9, 50.6, 49.4.
HRMS (ESI): m/z calcd for [C27H28N2O2 + H]+: 413.22235; found: 413.22128.
1,4-Dibenzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]piperazin-2-one (3d)
1,4-Dibenzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]piperazin-2-one (3d)
Compound 3d was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (37.2 mg, 84%) as a light yellow oil.
IR (ATR): 2935, 1651, 1588, 1154, 734, 698 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.40–7.17 (m, 10 H), 6.65 (d, J = 2.1 Hz, 2 H), 6.42 (s, 1 H), 5.58 (s, 1 H), 5.42 (s, 1 H), 4.76 (d, J = 14.7 Hz, 1 H), 4.36 (d, J = 14.7 Hz, 1 H), 4.16 (d, J = 13.0 Hz, 1 H), 3.77 (s, 6 H), 3.64–3.36 (m, 3 H), 3.23 (dd, J = 12.2, 4.1 Hz, 1 H), 3.12 (d, J = 13.0 Hz, 1 H), 2.98 (d, J = 17.0 Hz, 1 H).
13C NMR (101 MHz, CDCl3): δ = 167.2, 160.7, 145.7, 141.8, 137.5, 136.5, 128.8, 128.7, 128.4, 128.2, 127.6, 127.4, 118.1, 105.1, 99.9, 63.7, 58.3, 55.7, 55.4, 50.3, 49.4.
HRMS (ESI): m/z calcd for [C28H30N2O3 + H]+: 443.23292; found: 443.23235.
1,4-Dibenzyl-5-[1-(3,4-dichlorophenyl)vinyl]piperazin-2-one (3e)
1,4-Dibenzyl-5-[1-(3,4-dichlorophenyl)vinyl]piperazin-2-one (3e)
Compound 3e was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (26.2 mg, 58%) as an orange oil.
IR (ATR): 2922, 1647, 1453, 908, 728, 697 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.68 (d, J = 1.6 Hz, 1 H), 7.37–7.21 (m, 12 H), 5.56 (s, 1 H), 5.40 (s, 1 H), 4.77 (d, J = 14.6 Hz, 1 H), 4.39 (d, J = 14.6 Hz, 1 H), 4.03 (d, J = 12.9 Hz, 1 H), 3.63 (dd, J = 8.8, 4.5 Hz, 1 H), 3.54 (d, J = 17.1 Hz, 1 H), 3.40 (dd, J = 12.2, 9.0 Hz, 1 H), 3.25 (dd, J = 12.3, 4.4 Hz, 1 H), 3.19 (d, J = 13.0 Hz, 1 H), 3.00 (d, J = 17.1 Hz, 1 H).
13C NMR (101 MHz, CDCl3): δ = 167.1, 143.6, 139.1, 136.9, 136.3, 132.6, 132.1, 130.3, 128.8, 128.7, 128.7, 128.6, 128.5, 128.24, 127.7, 127.6, 126.1, 119.2, 63.0, 58.2, 55.1, 49.4, 48.9.
HRMS (ESI): m/z calcd for [C26H24Cl2N2O + H]+: 451.13385; found: 451.13339.
4-Allyl-1-benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]piperazin-2-one (3f)
4-Allyl-1-benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]piperazin-2-one (3f)
Compound 3f was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (26.1 mg, 66%) as an orange oil.
IR (ATR): 2929, 1652, 1589, 1453, 1154, 697 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.33–7.19 (m, 5 H), 6.65 (d, J = 2.1 Hz, 2 H), 6.41 (s, 1 H), 5.89–5.64 (m, 1 H), 5.52 (s, 1 H), 5.31 (s, 1 H), 5.19 (t, J = 12.8 Hz, 2 H), 4.79 (d, J = 14.7 Hz, 1 H), 4.32 (d, J = 14.7 Hz, 1 H), 3.82–3.67 (m, 7 H), 3.63–3.43 (m, 2 H), 3.40–3.29 (m, 1 H), 3.14 (dd, J = 12.1, 4.1 Hz, 1 H), 3.02 (d, J = 17.0 Hz, 1 H), 2.77 (dd, J = 13.5, 7.6 Hz, 1 H).
13C NMR (101 MHz, CDCl3): δ = 167.3, 160.7, 145.3, 141.6, 136.5, 134.0, 128.6, 128.1, 127.5, 118.6, 118.6, 105.1, 99.8, 63.8, 56.8, 55.7, 55.4, 50.2, 49.3.
HRMS (ESI): m/z calcd for [C24H28N2O3 + H]+: 393.21727; found: 393.21712.
1-Benzyl-4-hexyl-5-(1-naphthalen-2-ylvinyl)piperazin-2-one (3g)
1-Benzyl-4-hexyl-5-(1-naphthalen-2-ylvinyl)piperazin-2-one (3g)
Compound 3g was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (27.9 mg, 65%) as an orange oil.
IR (ATR): 2926, 1651, 1453, 1270, 820, 699 cm–1.
1H NMR (400 MHz, CDCl3): δ = 8.01 (s, 1 H), 7.82–7.74 (m, 3 H), 7.58 (dd, J = 8.6, 1.7 Hz, 1 H), 7.49–7.43 (m, 2 H), 7.30–7.22 (m, 5 H), 5.63 (s, 1 H), 5.38 (s, 1 H), 4.83 (d, J = 14.7 Hz, 1 H), 4.28 (d, J = 14.7 Hz, 1 H), 3.84 (d, J = 16.9 Hz, 1 H), 3.63 (dd, J = 9.7, 4.0 Hz, 1 H), 3.40 (dd, J = 12.0, 9.9 Hz, 1 H), 3.18 (dd, J = 12.1, 4.1 Hz, 1 H), 3.05 (d, J = 16.9 Hz, 1 H), 2.93–2.86 (m, 1 H), 2.20–2.13 (m, 1 H), 1.50–1.44 (m, 2 H), 1.30 (s, 2 H), 1.20 (d, J = 3.3 Hz, 2 H), 0.89 (d, J = 3.6 Hz, 2 H), 0.82 (t, J = 6.8 Hz, 3 H).
13C NMR (101 MHz, CDCl3): δ = 167.5, 145.5, 136.8, 136.5, 133.2, 132.9, 128.6, 128.3, 128.2, 127.9, 127.5, 126.3, 126.2, 125.7, 124.9, 118.4, 64.6, 55.8, 53.9, 50.2, 49.3, 31.7, 26.3, 26.6, 22.6, 14.0.
HRMS (ESI): m/z calcd for [C29H34N2O + H]+: 427.27439; found: 427.27465.
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-propylpiperazin-2-one (3h)
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-propylpiperazin-2-one (3h)
Compound 3h was synthesized following the general procedure. Flash chromatography (SiO2, 2:1 v/v PE–Et2O) afforded the product (38.0 mg, 96%) as an orange oil.
IR (ATR): 2960, 1652, 1589, 1203, 1154, 698 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.32–7.22 (m, 5 H), 6.66 (d, J = 2.0 Hz, 2 H), 6.40 (s, 1 H), 5.50 (s, 1 H), 5.28 (s, 1 H), 4.80 (d, J = 14.7 Hz, 1 H), 4.30 (d, J = 14.7 Hz, 1 H), 3.81–3.76 (m, 7 H), 3.46 (dd, J = 9.7, 3.9 Hz, 1 H), 3.41–3.28 (m, 1 H), 3.11 (dd, J = 12.0, 3.9 Hz, 1 H), 3.00 (d, J = 16.9 Hz, 1 H), 2.82 (dt, J = 12.1, 8.3 Hz, 1 H), 2.17–2.05 (m, 1 H), 1.56–1.46 (m, 2 H), 0.86 (t, J = 7.3 Hz, 3 H).
13C NMR (101 MHz, CDCl3): δ = 167.4, 160.6, 145.5, 141.7, 136.5, 128.6, 128.1, 127.5, 118.4, 105.1, 99.8, 64.5, 55.8, 55.8, 55.3, 50.2, 49.3, 19.9, 11.6.
HRMS (ESI): m/z calcd for [C24H30N2O3 + H]+: 395.23292; found: 395.23166.
1-Benzyl-5-(1-naphthalen-2-ylvinyl)-4-phenethylpiperazin-2-one (3i)
1-Benzyl-5-(1-naphthalen-2-ylvinyl)-4-phenethylpiperazin-2-one (3i)
Compound 3i was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (36.5 mg, 82%) as an orange oil.
IR (ATR): 3026, 1651, 1495, 1129, 909, 698 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.90 (s, 1 H), 7.81–7.76 (m, 1 H), 7.73 (dd, J = 8.8, 3.7 Hz, 2 H), 7.51 (d, J = 8.6 Hz, 1 H), 7.46 (dd, J = 6.3, 2.8 Hz, 2 H), 7.32–7.25 (m, 3 H), 7.25–7.15 (m, 5 H), 7.07 (d, J = 7.2 Hz, 2 H), 5.60 (s, 1 H), 5.32 (s, 1 H), 4.83 (d, J = 14.7 Hz, 1 H), 4.27 (d, J = 14.7 Hz, 1 H), 3.96 (d, J = 16.8 Hz, 1 H), 3.70 (dd, J = 9.7, 4.0 Hz, 1 H), 3.41–3.32 (m, 1 H), 3.18 (ddd, J = 20.7, 19.5, 12.6 Hz, 3 H), 2.77 (t, J = 7.8 Hz, 2 H), 2.57–2.46 (m, 1 H).
13C NMR (101 MHz, CDCl3): δ = 167.3, 145.3, 139.6, 136.7, 136.4, 133.2, 132.9, 128.7, 128.7, 128.4, 128.3, 128.1, 127.9, 127.6, 127.5, 126.2, 126.2, 126.1, 125.6, 124.9, 118.6, 64.2, 55.8, 55.6, 50.2, 49.4, 33.3.
HRMS (ESI): m/z calcd for [C31H30N2O + H]+: 447.24309; found: 447.24324.
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-[2-(1H-indol-3-yl)ethyl]piperazin-2-one (3j)
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-[2-(1H-indol-3-yl)ethyl]piperazin-2-one (3j)
Compound 3j was synthesized following the general procedure. Flash chromatography (SiO2, Et2O) afforded the product (25.6 mg, 51%) as an orange oil.
IR (ATR): 2928, 1639, 1589, 1154, 908, 730 cm–1.
1H NMR (400 MHz, CDCl3): δ = 8.04 (s, 1 H), 7.45 (d, J = 7.9 Hz, 1 H), 7.32–7.22 (m, 6 H), 7.15 (t, J = 7.5 Hz, 1 H), 7.05 (t, J = 7.4 Hz, 1 H), 6.91 (d, J = 1.7 Hz, 1 H), 6.64 (d, J = 2.1 Hz, 2 H), 6.40 (s, 1 H), 5.48 (s, 1 H), 5.26 (s, 1 H), 4.79 (d, J = 14.7 Hz, 1 H), 4.36 (d, J = 14.7 Hz, 1 H), 3.98 (d, J = 16.8 Hz, 1 H), 3.74 (s, 6 H), 3.59 (dd, J = 9.6, 3.9 Hz, 1 H), 3.43–3.32 (m, 1 H), 3.29–3.12 (m, 3 H), 3.02–2.81 (m, 2 H), 2.57–2.42 (m, 1 H).
13C NMR (101 MHz, CDCl3): δ = 167.4, 160.7, 145.5, 141.8, 136.5, 136.2, 128.7, 128.1, 127.5, 127.4, 121.9, 121.7, 119.2, 118.7, 118.2, 113.7, 111.1, 105.2, 99.8, 63.9, 55.9, 55.3, 54.5, 50.3, 49.4, 30.3, 23.0.
HRMS (ESI). m/z calcd for [C31H33N3O3 + H]+: 496.25947; found: 496.25915.
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-(3-hydroxypropyl)piperazin-2-one (3k)
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-(3-hydroxypropyl)piperazin-2-one (3k)
Compound 3k was synthesized following the general procedure. Flash chromatography (SiO2, EtOAc) afforded the product (24.4 mg, 60%) as an orange oil.
IR (ATR): 2933, 1636, 1589, 1203, 1154, 1062 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.38–7.21 (m, 5 H), 6.53 (d, J = 2.0 Hz, 2 H), 6.41 (s, 1 H), 5.54 (s, 1 H), 5.26 (s, 1 H), 4.73 (d, J = 14.6 Hz, 1 H), 4.43 (d, J = 14.6 Hz, 1 H), 3.88 (s, 1 H), 3.77 (s, 6 H), 3.68–3.55 (m, 2 H), 3.43–3.34 (m, 1 H), 3.23 (dd, J = 12.3, 4.1 Hz, 1 H), 3.14–3.00 (m, 2 H), 2.84–2.73 (m, 1 H), 2.42–2.32 (m, 1 H), 2.06 (s, 1 H), 1.84–1.76 (m, 1 H), 1.66–1.58 (m, 1 H).
13C NMR (101 MHz, CDCl3): δ = 166.8, 160.8, 145.6, 142.0, 136.3, 128.7, 128.2, 127.7, 117.8, 105.0, 104.3, 99.7, 63.2, 62.5, 55.4, 55.2, 52.2, 49.8, 49.5, 28.5.
HRMS (ESI): m/z calcd for [C24H30N2O4 + H]+: 411.22783; found: 411.22693.
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-pyridin-2-ylmethylpiperazin-2-one (3l)
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-pyridin-2-ylmethylpiperazin-2-one (3l)
Compound 3l was synthesized following the general procedure. Flash chromatography (SiO2, EtOAc) afforded the product (28.3 mg, 64%) as an orange oil.
IR (ATR): 2936, 1651, 1589, 1204, 1154, 727 cm–1.
1H NMR (400 MHz, CDCl3): δ = 8.53 (d, J = 4.3 Hz, 1 H), 7.63 (t, J = 8.1 Hz, 1 H), 7.29 (dt, J = 15.4, 8.1 Hz, 6 H), 7.18–7.13 (m, 1 H), 6.64 (d, J = 1.6 Hz, 2 H), 6.41 (s, 1 H), 5.56 (s, 1 H), 5.42 (s, 1 H), 4.76 (d, J = 14.7 Hz, 1 H), 4.38 (d, J = 14.7 Hz, 1 H), 4.29 (d, J = 13.9 Hz, 1 H), 3.76 (d, J = 10.1 Hz, 6 H), 3.75–3.70 (m, 1 H), 3.60 (d, J = 17.0 Hz, 1 H), 3.50–3.37 (m, 2 H), 3.27 (dd, J = 12.2, 4.0 Hz, 1 H), 3.14 (d, J = 17.0 Hz, 1 H).
13C NMR (101 MHz, CDCl3): δ = 167.0, 160.7, 158.0, 149.3, 145.6, 141.9, 136.6, 136.4, 132.2, 132.1, 128.7, 128.4, 128.2, 127.6, 122.7, 122.2, 118.3, 105.2, 99.8, 63.5, 59.8, 56.0, 55.4, 50.2, 49.4.
HRMS (ESI): m/z calcd for [C27H29 N3O3 + H]+: 444.22817; found: 444.22770.
{3-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]propyl}carbamic Acid tert-Butyl Ester (3m)
{3-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]propyl}carbamic Acid tert-Butyl Ester (3m)
Compound 3m was synthesized following the general procedure. Flash chromatography (SiO2, Et2O) afforded the product (27.1 mg, 56%) as a thick, yellow oil.
IR (ATR): 2973, 1699, 1645, 1497, 1168, 728 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.91 (s, 1 H), 7.79 (dd, J = 11.1, 5.7 Hz, 3 H), 7.54 (d, J = 8.5 Hz, 1 H), 7.49–7.45 (m, 2 H), 7.34–7.22 (m, 5 H), 5.64 (s, 1 H), 5.35 (s, 1 H), 4.76 (d, J = 14.6 Hz, 1 H), 4.55 (s, 1 H), 4.40 (d, J = 14.6 Hz, 1 H), 3.80 (d, J = 16.9 Hz, 1 H), 3.71 (dd, J = 9.3, 3.9 Hz, 1 H), 3.49–3.37 (m, 1 H), 3.24 (dd, J = 12.2, 4.0 Hz, 1 H), 3.12–3.07 (m, 3 H), 2.92 (dt, J = 12.6, 7.6 Hz, 1 H), 2.30–2.20 (m, 1 H), 1.64 (dd, J = 14.4, 7.2 Hz, 2 H), 1.37 (s, 9 H).
13C NMR (101 MHz, CDCl3): δ = 167.1, 155.8, 145.5, 143.3, 136.8, 136.4, 133.2, 132.9, 130.5, 128.9, 128.7, 128.4, 128.2, 128.2, 128.1, 127.6, 127.5, 126.4, 126.3, 125.4, 124.7, 118.1, 78.9, 63.6, 55.3, 51.3, 49.9, 49.4, 38.6, 30.3, 28.4, 26.9.
HRMS (ESI): m/z calcd for [C31H37N3O3 + Na]+: 522.27271; found: 522.27227.
6-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]hexanoic Acid Methyl Ester (3n)
6-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]hexanoic Acid Methyl Ester (3n)
Compound 3n was synthesized following the general procedure. Flash chromatography (SiO2, Et2O) afforded the product (29.5 mg, 63%) as an orange oil.
IR (ATR): 2929, 1733, 1651, 1434, 1170, 728 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.99 (s, 1 H), 7.78 (t, J = 5.9 Hz, 3 H), 7.57 (d, J = 8.5 Hz, 1 H), 7.49–7.44 (m, 2 H), 7.27 (dt, J = 16.1, 7.1 Hz, 5 H), 5.63 (s, 1 H), 5.37 (s, 1 H), 4.81 (d, J = 14.7 Hz, 1 H), 4.30 (d, J = 14.7 Hz, 1 H), 3.81 (d, J = 16.9 Hz, 1 H), 3.68–3.60 (m, 4 H), 3.49–3.34 (m, 1 H), 3.19 (dd, J = 12.1, 3.9 Hz, 1 H), 3.05 (d, J = 16.9 Hz, 1 H), 2.89 (dt, J = 12.3, 7.9 Hz, 1 H), 2.21 (t, J = 7.5 Hz, 2 H), 1.61–1.47 (m, 5 H), 1.32 (dd, J = 14.2, 6.8 Hz, 1 H), 1.21 (dd, J = 14.0, 6.5 Hz, 1 H).
13C NMR (101 MHz, CDCl3): δ = 174.0, 167.4, 145.4, 136.7, 136.5, 133.2, 132.9, 128.6, 128.2, 128.2, 127.9, 127.5, 127.5, 126.3, 126.2, 125.6, 124.9, 118.4, 64.4, 55.6, 53.6, 51.4, 50.1, 49.4, 33.9, 26.6, 26.3, 24.8.
HRMS (ESI): m/z calcd for [C30H34N2O3 + H]+: 471.26422; found: 471.26375.
[2-(2-{2-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]ethoxy}ethoxy)ethyl]carbamic Acid tert-Butyl Ester (3o)
[2-(2-{2-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]ethoxy}ethoxy)ethyl]carbamic Acid tert-Butyl Ester (3o)
Compound 3o was synthesized following the general procedure. Flash chromatography (SiO2, EtOAc) afforded the product (29.0 mg, 51%) as an orange oil.
IR (ATR): 2867, 1704, 1645, 1171, 1118, 697 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.95 (s, 1 H), 7.79 (dd, J = 5.5, 3.1 Hz, 2 H), 7.67 (dd, J = 11.8, 7.1 Hz, 1 H), 7.55 (d, J = 1.7 Hz, 1 H), 7.49–7.46 (m, 2 H), 7.27 (dt, J = 10.3, 7.5 Hz, 5 H), 5.64 (s, 1 H), 5.39 (s, 1 H), 5.17 (s, 1 H), 4.79 (d, J = 14.6 Hz, 1 H), 4.33 (d, J = 14.7 Hz, 1 H), 3.95 (d, J = 17.1 Hz, 1 H), 3.77 (dd, J = 9.4, 4.0 Hz, 1 H), 3.65–3.45 (m, 8 H), 3.46–3.37 (m, 1 H), 3.25 (dt, J = 7.8, 5.6 Hz, 4 H), 3.18–3.10 (m, 1 H), 2.55–2.43 (m, 1 H), 1.43 (s, 9 H).
13C NMR (101 MHz, CDCl3): δ = 167.4, 156.1, 145.5, 136.9, 136.5, 133.2, 132.9, 132.2, 132.2, 132.1, 132.1, 131.9, 131.9, 129.0, 128.7, 128.6, 128.6, 128.5, 128.4, 128.3, 128.2, 127.9, 127.6, 127.5, 126.9, 126.3, 126.2, 125.6, 124.9, 118.4, 79.1, 70.4, 70.3, 70.2, 69.5, 63.9, 56.5, 52.9, 49.9, 49.4, 40.4, 28.4.
HRMS (ESI): m/z calcd for [C34H43N3O5 + H]+: 574.32755; found: 574.33039.
4-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]butyric Acid Methyl Ester (3p)
4-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]butyric Acid Methyl Ester (3p)
Compound 3p was synthesized following the general procedure. Flash chromatography (SiO2, Et2O) afforded the product (27.1 mg, 61%) as a yellow oil.
IR (ATR): 2923, 1732, 1651, 1258, 1129, 699 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.93 (s, 1 H), 7.79 (dd, J = 12.2, 8.9 Hz, 3 H), 7.53 (d, J = 8.6 Hz, 1 H), 7.50–7.44 (m, 2 H), 7.28 (dt, J = 15.8, 7.5 Hz, 5 H), 5.63 (s, 1 H), 5.36 (s, 1 H), 4.77 (d, J = 14.6 Hz, 1 H), 4.36 (d, J = 14.7 Hz, 1 H), 3.82 (d, J = 16.9 Hz, 1 H), 3.68 (dd, J = 9.4, 4.0 Hz, 1 H), 3.55 (s, 3 H), 3.40 (dd, J = 18.9, 9.4 Hz, 1 H), 3.22 (dd, J = 12.2, 4.1 Hz, 1 H), 3.08 (d, J = 16.9 Hz, 1 H), 2.93 (dt, J = 12.4, 7.9 Hz, 1 H), 2.37–2.20 (m, 3 H), 1.81 (dd, J = 11.7, 5.8 Hz, 2 H).
13C NMR (101 MHz, CDCl3): δ = 173.7, 167.2, 145.4, 136.8, 136.4, 133.2, 132.9, 128.9, 128.3, 128.2, 128.0, 127.6, 127.5, 126.3, 126.2, 125.5, 124.8, 118.2, 63.9, 55.4, 52.8, 51.4, 50.1, 49.4, 31.3, 21.9.
HRMS (ESI): m/z calcd for [C28H30N2O3 + H]+: 443.23292; found: 443.23237.
{4-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]butyl}carbamic Acid tert-Butyl Ester (3q)
{4-[4-Benzyl-2-(1-naphthalen-2-ylvinyl)-5-oxopiperazin-1-yl]butyl}carbamic Acid tert-Butyl Ester (3q)
Compound 3q was synthesized following the general procedure. Flash chromatography (SiO2, Et2O) afforded the product (25.7 mg, 50%) as a light yellow oil.
IR (ATR): 2929, 1704, 1645, 1502, 1167, 733 cm–1.
1H NMR (400 MHz, CDCl3): δ = 7.96 (s, 1 H), 7.82–7.74 (m, 3 H), 7.55 (d, J = 8.6 Hz, 1 H), 7.51–7.42 (m, 2 H), 7.28 (ddd, J = 15.9, 12.2, 6.7 Hz, 5 H), 5.64 (s, 1 H), 5.36 (s, 1 H), 4.80 (d, J = 14.7 Hz, 1 H), 4.46 (s, 1 H), 4.33 (d, J = 14.7 Hz, 1 H), 3.80 (d, J = 16.9 Hz, 1 H), 3.67 (dd, J = 9.5, 4.0 Hz, 1 H), 3.47–3.38 (m, 1 H), 3.21 (dd, J = 12.2, 4.1 Hz, 1 H), 3.04 (dd, J = 18.2, 11.2 Hz, 3 H), 2.94–2.83 (m, 1 H), 2.27–2.16 (m, 1 H), 1.48 (s, 4 H), 1.42 (s, 9 H).
13C NMR (101 MHz, CDCl3): δ = 167.3, 155.9, 145.4, 136.8, 136.5, 133.2, 132.9, 128.7, 128.2, 128.2, 127.9, 127.6, 127.5, 126.3, 126.2, 125.6, 124.8, 118.2, 79.1, 64.1, 55.5, 53.3, 50.0, 49.4, 40.3, 30.3, 28.4, 27.6, 23.9.
HRMS (ESI): m/z calcd for [C32H39N3O3 + H]+: 514.30642; found: 514.07750.
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-hexylpiperazin-2-one (4)
1-Benzyl-5-[1-(3,5-dimethoxyphenyl)vinyl]-4-hexylpiperazin-2-one (4)
Compound 4 was synthesized following the general procedure. Flash chromatography (SiO2, 1:2 v/v PE–Et2O) afforded the product (28.8 mg, 66%) as an orange oil.
IR (ATR): 2927, 1652, 1590, 1204, 1154, 698 cm1.
1H NMR (400 MHz, CDCl3): δ = 7.32–7.22 (m, 5 H), 6.65 (d, J = 2.1 Hz, 2 H), 6.40 (s, 1 H), 5.50 (s, 1 H), 5.28 (s, 1 H), 4.80 (d, J = 14.7 Hz, 1 H), 4.30 (d, J = 14.7 Hz, 1 H), 3.82 (d, J = 9.4 Hz, 1 H), 3.76 (s, 6 H), 3.46 (dd, J = 9.7, 4.0 Hz, 1 H), 3.38–3.29 (m, 1 H), 3.11 (dd, J = 12.0, 3.9 Hz, 1 H), 2.99 (d, J = 16.9 Hz, 1 H), 2.85 (dt, J = 12.2, 8.1 Hz, 1 H), 2.17–2.07 (m, 1 H), 1.51–1.44 (m, 2 H), 1.31–1.21 (m, 6 H), 0.86 (t, J = 6.8 Hz, 3 H).
13C NMR (101 MHz, CDCl3): δ = 167.4, 160.7, 145.5, 141.8, 136.5, 128.6, 128.1, 127.5, 118.3, 105.2, 99.8, 64.5, 55.8, 55.3, 54.0, 50.3, 49.3, 31.8, 26.9, 26.7, 22.6, 14.0.
HRMS (ESI): m/z calcd for [C27H36N2O3 + H]+: 514.30642; found: 514.30775.
