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DOI: 10.1055/s-2008-1032104
Novel Catalytic Synthetic Route to Protected α-Methyl Threonine and the First Asymmetric Acetyl Migration in a Steglich Rearrangement Reaction
Publication History
Publication Date:
26 February 2008 (online)
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Abstract
A short synthetic route to protected a-methyl threonine 5 as a representative example for (protected) a-methylated a-amino-b-hydroxy acids bearing a stereogenic quaternary carbon center in a-position was developed. This multistep synthesis is based on the use of an easily accessible prochiral starting material in the presence of an organocatalyst, and allows the access to all four types of stereoisomers. In addition, the first enantioselective acetyl migration in a Steglich rearrangement reaction as a key step in this multistep synthesis of 5 was achieved. The heterocycle 12, which was used in Steglich rearrangement reaction for the first time, turned out to be an efficient organocatalyst leading to an enantioselectivity of up to 63% ee.
Key words
acylation - amino acids - asymmetric catalysis - rearrangements - stereoselective synthesis
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References and Notes
Preparation of rac -4-Acetyl-4-methyl-2-phenyloxazol-5-one ( rac -7)In analogy to a protocol described in ref. 8, 5-acetyloxy-4-methyl-2-phenyloxazole (8, 2.0 g, 9.3 mmol) and DMAP (10, 90 mg, 0.7 mmol) were dissolved in CH2Cl2 (50 mL) at r.t. After 3 h of stirring, the solvent was removed to give 7 (2.05 g, 9.4 mmol, purity >95%) as yellow oil. 1H NMR (400 MHz, CDCl3): d = 1.69 (3 H, s), 2.27 (3 H, s), 7.45-7.60 (3 H, m), 8.00-8.02 (2 H, m) ppm. 13C NMR (100 MHz, CDCl3): d = 20.95, 25.84, 77.96, 125.20,128.10, 128.87, 133.28, 162.61, 174.42, 198.39 ppm. MS-FAB: m/z = 218, 176.
10Preparation of rac -2-Benzoylamino-2-methyl-3-oxobutyric Acid Isopropyl Ester ( rac -6)4-Acetyl-4-methyl-2-phenyloxazol-5-one (rac- 7, 1.5 g, 6.9 mmol) and DMAP (10, 90 mg, 0.7 mmol) were dissolved in i-PrOH (40 mL). The reaction mixture was stirred for 16 h and the excess of i-PrOH was removed in vacuo. The resulting crude product was purified by column chromatography [SiO2 60 Å, cyclohexane-EtOAc (3:1)] to give rac-6 (1.62 g, 5.8 mmol, 84% yield). 1H NMR (400 MHz, CDCl3): d = 1.18 (3 H, d, J = 6.3 Hz), 1.21 (3 H, d, J = 6.3 Hz), 1.79 (3 H, s), 2.21 (3 H, s), 5.08 (1 H, sept, J = 6.3 Hz), 7.40-7.44 (2 H, m), 7.48-7.52 (1 H, m), 7.71 (1 H, br s), 7.78-7.81 (2 H, m) ppm. 13C NMR (100 MHz, CDCl3): d = 19.97, 21.36, 21.39, 23.97, 68.62, 70.51, 127.02, 128.58, 131.84, 133.51, 165.85, 168.56, 200.23 ppm. MS (EI): m/z = 278, 234. IR: 3412, 3327, 2984, 1722, 1664 cm-1. Anal. Calcd (%) for C15H19NO4: C, 64.97; H, 6.91; N, 5.05. Found: C, 64.61; H, 6.88; N, 4.89.
11Preparation of Diastereomers of rac -2-Benzoylamino-3-hydroxy-2-methylbutyric Acid Isopropyl Ester ( rac - l -5, rac - u -5)2-Benzoylamino-2-methyl-3-oxobutyric acid isopropyl ester (rac-6, 200 mg, 0.72 mmol) was dissolved in i-PrOH (20 mL) and cooled in an ice bath. After adding NaBH4 (13.6 mg, 0.36 mmol) the mixture was stirred at ice-bath temperature for 2 h, and further 2 h at r.t. Subsequently, dilute HCl was added until no further hydrogen was evolved. After addition of H2O the reaction mixture was extracted 5 times with MTBE. Removal of the solvent furnished a crude product of the resulting racemic diastereomers l-5 and u-5 (dr = 60:40), which were separated by column chroma-tography [SiO2 60 Å, cyclohexane-EtOAc (3:1)] to give rac-l- 5 (36 mg, 0.13 mmol, 18%) and rac-u- 5 (37 mg, 0.13 mmol, 18%).Compound rac-l-5: R f = 0.16. 1H NMR (400 MHz, CDCl3): d = 1.07 (3 H, d, J = 6.5 Hz), 1.25-1.29 (6 H, m), 1.69 (3 H, s), 4.14-4.22 (1 H, m), 5.05-5.14 (1 H, m), 5.49 (1 H, d, J = 10.1 Hz), 7.41-7.45 (2 H, m), 7.48-7.53 (1 H, m), 7.61 (1 H, br s), 7.79-7.81 (2 H, m) ppm. 13C NMR (100 MHz, CDCl3): d = 18.67, 18.85, 21.49, 65.90, 70.53, 71.19, 127.09, 128.67, 131.99, 133.82, 167.89, 173.42 ppm. MS-FAB: m/z = 280. IR: 3516, 3242, 2984, 1706, 1633 cm-1. Anal. Calcd (%) for C15H21NO4: C, 64.50; H, 7.58; N, 5.01. Found: C, 62.82; H, 7.51; N, 4.75.Compound rac-u-5: R f = 0.06. 1H NMR (400 MHz, CDCl3): d = 1.20-1.26 (9 H, m), 1.58 (3 H, s), 3.71 (1 H, br s), 4.13-4.20 (1 H, m), 5.04-5.13 (1 H, m), 6.86 (1 H, br s), 7.38-7.42 (2 H, m), 7.46-7.50 (1 H, m), 7.74-7.77 (2 H, m) ppm. 13C NMR (100 MHz, CDCl3): d = 17.85, 18.60, 21.63, 21.69, 64.60, 69.57, 71.29, 127.00, 128.56, 131.67, 134.39, 167.83, 172.09 ppm. MS-FAB: m/z = 280. IR: 3412, 3331, 2976, 1733, 1640 cm-1. Anal. Calcd (%) for C15H21NO4: C, 64.50; H, 7.58; N, 5.01. Found: C, 64.13; H, 7.61; N, 4.87.
15Experimental Procedure (Exemplified for Reaction in Table 1, Entry 1)5-Acetyloxy-4-methyl-2-phenyloxazole (8, 500 mg, 2.3 mmol) and 4-dimethylaminopyridinyl-(pentaphenyl-cyclopentadienyl)iron [(S)-11, 40 mg, 0.06 mmol] were dissolved in CH2Cl2 (20 mL) and stirred at r.t. for 3 h. Subsequently the solvent was removed to give 4-acetyl-4-methyl-2-phenyloxazol-5-one 7 (537 mg) as an oily crude product. The conversion (84%) and enantioselectivity (25% ee) were determined by 1H NMR spectroscopy and chiral HPLC chromatography [after derivatization to 6, Daicel Chiralcel OD column, hexane/2-PrOH (97:3)], respectively. The spectroscopic properties are in accordance with those for the racemic product rac-7. The other reactions with catalyst (S)-11 (Table [1] , entries 2-4) as well as the reaction with (-)-tetramisole [(S)-12] as a catalyst in CH2Cl2 (Table [1] , entry 6) were carried out on a 2 mL scale using 100 mg of substrate 8. The reaction with (S)-12 as a catalyst (Table [1] , entry 5) was carried out on a 1 mL scale, and the conversion was directly determined from the reaction mixture by 1H NMR spectroscopy in this experiment.