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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 659873생성일: 2026년 10월 24일

Trimethylsilyl triflate → Phenyl 2-o-acetyl-3,5-di-o-benzyl-4-c-methanesulfonyloxymethyl-1-thio-beta-d-ribofuranoside

https://huagongshe.com/ko/reaction/659873

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참여 물질

역할이름HCID투입량
반응물Trimethylsilyl triflateHCID 65367—
반응물PhenylthiotrimethylsilaneHCID 78312—
반응물Methyl 2-O-acetyl-3,5-di-O-benzyl-4-C-methanesulfonyloxymethyl-D-ribofuranosideHCID 11145450—
용매DichloromethaneHCID 6344—
생성물Phenyl 2-o-acetyl-3,5-di-o-benzyl-4-c-methanesulfonyloxymethyl-1-thio-beta-d-ribofuranosideHCID 1094081766.1%

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온도0 °C

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Method a. A stirred solution of 209 (738 mg, 1.49 mmol) in anhydrous dichloromethane (6.4 mL) was added phenylthiotrimethylsilane (2.42 mL, 12.8 mmol) and cooled to 0° C. Trimethylsilyl triflate (0.67 mL, 3.67 mmol) was added dropwise and the solution was stirred at room temperature for 4 h. The reaction was quenched with a saturated aqueous solution of sodium hydrogen carbonate (100 mL) and extracted with dichloromethane (2×200 mL). The combined extract was dried (MgSO4) and the solvent removed by distillation under reduced pressure. The residue was purified by chromatography over silica gel with dichloromethane as eluent to give the product 210 as a clear oil (564 mg, 66%) and unreacted starting material (191 mg, 26%); Method b. A stirred solution of 211 (86 mg, 0.165 mmol) in anhydrous dichloromethane (0.49 mL) was added phenylthiotrimethylsilane (0.16 mL, 0.825 mmol) and cooled to 0° C. Trimethylsilyl triflate (0.037 mL, 0.206 mmol) was added and the solution was stirred at room temperature for 2 h. The reaction was quenched with a saturated aqueous solution of sodium hydrogen carbonate (15 mL) and the resulting mixture was extracted with dichloromethane (2×25 mL). The combined extract was dried (MgSO4) and the solvent removed by distillation under reduced pressure. The residue was purified by chromatography over silica gel with dichloromethane as eluent to give the product 210 as a clear oil (75 mg, 79%); 1H NMR (CDCl3): δ 7.47-7.19 (15H, m, Bn, SPh), 5.48 (1H, d, J 3.6 Hz, H-2), 5.34 (1H, dd, J 3.7, 5.2 Hz, H-1), 4.54-4.36 (7H, m, H-3, H-5□, Bn), 3.66 (1H, d, J 9.7 Hz, H-5), 3.48 (1H, d, J 9.5 Hz, H-5), 2.89 (3H, s, SO2CH3), 2.09 (3H, s, OCCH3); 13C NMR (CDCl3): δ 169.93 (C═O), 137.69, 137.08, 132.65, 132.45, 129.15, 128.53, 128.52, 128.18, 128.14, 128.08, 127.91, 127.85 (Bn, SPh), 87.99, 84.35, 80.34, 75.33, 74.20, 73.67, 70.83, 69.34 (C-1, C-2, C-3, C-4, C-5, C-5′, Bn), 37.27 (SO2CH3), 20.68 (OCCH3); MS FAB: 463 (M−SPh, 100%), 595 (M+Na, 24%). Found. C, 61.17; H, 5.55; C29H32O8S2 requires C, 60.82; H, 5.63%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08080644B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-7c84f743ee4a4ba297ed4ecbfd7bb6d9
출처 메모uspto-grants-2011_12