Application of Directed Metalation in Synthesis. Part 5: [1] [2] Synthesis of Condensed Sulfur-Oxygen Heterocycle via Novel Anionic Rearrangement-Cyclisation

Abstract

Introduction of the methyl sulfanyl function in the ortho-position to O-carbamate functionality under standard directed metalation condition was followed by side-chain deprotonation with sec-butyl lithium at -78 °C. Upon warming to room temperature, the deprotonated species underwent intramolecular anionic rearrangement to afford N,N-diethyl-2-hydroxyarylthioacetamides. The rearranged products were cyclised with hot glacial acetic acid to afford condensed oxathiin-2-ones in excellent yields.

directed metalation - anionic rearrangement - oxathiin-2-one

References

1 Part 4, see: Mukherjee C. Kamila S. De A. Tetrahedron  2003,  59:  4767 

2

Abstracted in part from the Ph.D. thesis submitted by C. M. to Jadavpur University, 2003.

3 Snieckus V. Chem. Rev.  1990,  90:  879 

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6 Sibi MP. Chattopadhay S. Dankwardt JW. Snieckus V. J. Am. Chem. Soc.  1985,  107:  6312 

7a Kamila S. Mukherjee C. De A. Tetrahedron Lett.  2001,  42:  5955 

7b Kamila S. Mukherjee C. Mondal SS. De A. Tetrahedron  2003,  1339 

8 Zhang P. Gawley RE. J. Org. Chem.  1993,  58:  3223 

9 Wang W. Snieckus V. J. Org. Chem.  1992,  57:  424 

10 Kalinin AV. Jalil Miah MA. Chattopadhay S. Tsukazaki M. Wicki M. Nguyen T. Coelho AL. Kerr M. Snieckus V. Synlett  1997,  839 

11

Representative Example of Synthesis of O -Aryl N , N -Diethyl Carbamates.
To a well stirred suspension of NaH (3 equiv), in anhyd THF (10 mL), a solution of 2-methoxy-4-methylphenol (28 mmol) in anhyd THF (10 mL) was added through a pressure equalising dropping funnel at r.t. After stirring the reaction mixture for 2 h, N,N-diethylcarbamylchloride (7.3 mL, 2 equiv) in THF (10 mL) was added to the reaction mixture. Stirring was continued for another 8 h. THF was removed in vacuo and usual aqueous work up afforded the crude product N,N-diethyl-1-carbamyloxy-2-methoxy-4-methylbenzene 1e which was purified by crystallisation (EtOAc:petroleum ether). Colourless needles, 95% yield; mp 51-53 °C. IR (neat): 1720 (C=O) cm^-1. ¹H NMR (300 MHZ, CDCl₃): δ = 1.23 (t, 6 H, -CH₂CH ₃), 2.34 (s, 3 H, -CH₃), 3.41 (q, 4 H, -CH ₂CH₃), 3.8 (s, 3 H, -OMe), 6.74 (dd, 1 H, J = 3.0, 8.0 Hz, Ar-5H), 6.76 (d, 1 H, J = 3.0 Hz, Ar-3H), 6.96 (d, 1 H, J = 8.0 Hz, Ar-6H). ¹³C (75 MHZ, CDCl₃): δ = 13.2, 13.8, 14.4, 21.8, 42.4, 42.5, 56.3, 113.7, 121.4, 123.2, 136.3, 138.7, 151.6, 154.7. Anal. Calcd for C₁₃H₁₉O₃N: C, 65.82; H, 8.01; N, 5.90. Found: C, 65.68; H, 7.87; N, 6.0.

12

Representative Example of Introduction of Methyl Sulfanyl Function by Directed Metalation. To a well stirred solution of TMEDA (5.5 mL, 2.5 equiv), anhyd THF (10 mL), sec-BuLi [26 mL of 1.4 M solution in cyclohexane, 2.5 equiv] kept at -78 °C under argon atmosphere, a solution of N,N-diethyl-1-carbamyloxy-2-methoxy-4-methylbenzene 1e (14.5 mmol), in THF (5 mL) was added via syringe. After stirring for 30 min at that temperature, dimethyl disulfide (3.3 mL, 2.5 equiv) was added and stirring continued for further 45 min at the same temperature. The reaction mixture was then allowed to warm to r.t. and stirred for 10 h. Usual ammonium chloride work up afforded the crude N,N-diethyl-1-carbamyloxy-2-methylsulfanylbenzene. Purification by crystallisation (EtOAc-petroleum ether) afforded N,N-diethyl-1-carbamyloxy-2-methylsulfanyl-4-methyl-6-methoxybenzene 2e. Yellowish needles, 96% yield; mp 31-33 °C. IR (neat): 1724 (C=O) cm^-1. ¹H NMR (300 MHz, CDCl₃): δ = 1.18-1.25 (t, 6 H, -CH₂CH ₃), 2.25 (s, 3 H, -Me), 2.33 (s, 3 H, -SMe), 3.35-3.37 (q, 4 H, -CH ₂CH₃), 3.72 (s, 3 H, -OMe), 6.49 (d, 1 H, J = 1.6 Hz, Ar-5H), 6.53 (d, 1 H, J = 1.6 Hz, Ar-3H). ¹³C (75 MHz, CDCl₃): δ = 14.0, 15.5, 22.1, 42.5, 56.5, 110.6, 118.6, 133.1, 135.7, 136.4, 152.1, 153.7. Anal. Calcd for C₁₄H₂₁O₃NS: C, 59.36; H, 7.42; N, 4.94. Found: C, 59.18; H, 6.99; N, 5.0.

13 Mukherjee C. De A. Synlett  2002,  325 

14

Representative Example of Preparation of N , N -Diethyl-2-hydroxy Aryl Thioacetamide. To a stirred solution of TMEDA (0.54 mL, 2.5 equiv), sec-BuLi (2.01 mL of 1.8 M solution, 2.5 equiv). in anhyd THF (7 mL) kept at -78 °C in argon atmosphere, a solution of N,N-diethyl-1-carbamyloxy-2-methylsulfanyl-4-methyl-6-methoxybenzene 2e (14.5 mmol), in dry THF (3 mL) was added via syringe. Stirring was continued for 1 h at that temperature, then the reaction mixture was allowed to attain r.t. and kept for 8 h. Ammonium chloride work up afforded crude material which was purified by crystallisation (EtOAc-petroleum ether) to obtain N,N-diethyl-2-hydroxy-3-methoxy-5-methylphenylthioacetamide 3d, 85% yield. IR (KBr): 3120 (-OH), 1624 (C=O) cm^-1. ¹H NMR (300 MHz, CDCl₃): δ = 1.09 (t, 6 H, -CH₂CH ₃), 2.21 (s, 3 H, -CH₃), 3.30 (q, 4 H, -CH ₂CH₃), 3.61 (s, 2 H, -SCH₂-), 3.82 (s, 3 H, -OMe), 6.65 (d, 1 H, J = 1.6 Hz, Ar-4H), 6.87 (d, 1 H, J = 1.6 Hz, Ar-6H). ¹³C (75 MHz, CDCl₃): δ = 13.2, 14.58, 21.2, 39.3, 41.6, 42.7, 56.5, 114.5, 119.3, 128.2, 129.3, 146.6, 148.4, 169.3. Anal. Calcd for C₁₄H₂₁O₃NS: C, 59.36; H, 7.4; N, 4.9. Found: C, 59.4; H, 7.5; N, 5.1.

15

Synthesis of N , N -Diethyl-2-hydroxy-3-methyl Sulfanyl Benzamide. To a stirred solution of TMEDA (1.34 mL, 3 equiv) was added sec-BuLi (4.0 mL of 1.9 M solution in cyclohexane, 2.5 equiv) in anhyd THF (7 mL) kept at -78 °C in argon atmosphere, a solution of N,N-diethyl-1-carbamyloxy-2-methylsulfanylbenzene 2a (3.0 mmol) in dry THF (3 mL) was added via syringe. Stirring was continued for 1 h at that temperature, then the mixture was allowed to attain r.t. and kept for 8 h. Ammonium chloride work up afforded crude N,N-diethyl-2-hydroxy-3-methyl sulfanyl benzamide 3a which was purified by crystallisation (EtOAc-petroleum ether). Yellowish needles, 89% yield; mp 56-58 °C. IR (KBr): 3057 (-OH), 1604 (C=O) cm^-1. ¹H NMR (300 MHz, CDCl₃): δ = 1.16 (t, 6 H, -CH₂CH ₃), 2.34 (s, 3 H, -SMe), 3.37-3.45 (q, 4 H, -CH ₂CH₃), 6.80 (dd, 1 H, J = 7.7, 7.7 Hz, Ar-4H), 7.07 (dd, 1 H, J = 1.3, 7.7 Hz, Ar-3H), 7.26 (dd, 1 H, J = 1.3, 7.7 Hz, Ar-5H). ¹³C (75 MHz, CDCl₃): δ = 13.8, 16.9, 42.3, 119.7, 125.9, 126.04, 127.6, 131.6, 155.2, 170.7. Anal. Calcd for C₁₂H₁₇O₂NS: C, 62.88; H, 7.4; N, 6.1. Found: C, 63; H, 7.5; N, 6.2.

16

Representative Example of Preperation of Benz[1,4]oxathiin-2-ones:
Hydroxy compound 3d (0.88 mmol) was refluxed with glacial acetic acid (7 mL) for 18 h under magnetic stirring. After cooling, the reaction mixture was extracted with CH₂Cl₂ (2 × 100 mL). The organic layer was washed with H₂O and dried (Na₂SO₄). Removal of solvent afforded crude 6-methyl-8-methoxy-benz[1,4]oxathiin-2-one 5d which was purified by crystallisation (EtOAc-light petroleum), 83% yield; mp 117-121 °C. IR (KBr): 1759 (C=O) cm^-1. ¹H NMR (300 MHz, CDCl₃): δ = 2.3 (s, 3 H, -CH₃), 3.41 (s, 2 H, -SCH_2-), 3.85 (s, 3 H, -OMe), 6.63 (s, 1 H, Ar-5H), 6.69 (s, 1 H, Ar-7H). ¹³C NMR (75 MHz, CDCl₃): δ = 21.6, 29.1, 56.5, 112.1, 119.9, 120.7, 135.2, 138.6, 148.8, 163.1. Anal. Calcd for C₁₀H₁₀O₃S: C, 57.14; H, 4.76. Found: C, 57.2; H, 4.62.

17 Marks IE. In Comprehensive Organic Synthesis   Vol. 3:  Trost BM. Fleming I. Pergamon; Oxford: 1992.  p.913 

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