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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 653981생성일: 2026년 10월 26일

Chlorotrimethylsilane → HCID 15126108, 화합물

https://huagongshe.com/reaction/653981

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물HexamethyldisilazaneHCID 13838—
반응물Sodium BicarbonateHCID 516892—
반응물1-O-Acetyl-5-O-t-butyldiphenylsilyl-4-thio-2,3-dideoxyribofuranoseHCID 15126098—
반응물Potassium perfluorobutanesulfonateHCID 23675274—
반응물CytosineHCID 178418229—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물HCID 15126108HCID 15126108—

반응 조건

온도25 °C

반응 단계

A mixture of 10 (0.26 g, 0.63 mmol), cytosine (0.105 g, 0.95 mmol), and potassium nonafluorobutanesulfonate (0.77 g, 2.3 mmol) was suspended in 12 mL dry acetonitrile under nitrogen. HMDS (0.135 mL, 0.63 mmol) and TMS-Cl (0.37 mL, 2.9 mmol) were added sequentially via syringe and the reaction stirred at 25° C. overnight. The reaction was poured into a mixture of 20 mL dichloromethane and 15 mL saturated NaHCO3 and shaken. The organic phase was dried (MgSO4) and concentrated in vacuo. The anomeric mixture was separated by preparative TLC with 7.5% MeOH/CHCl3 with an ammonia atmosphere: yield of β-anomer, 78 mg and 117 mg of the α-anomer to afford total yield of 195 mg (66.5%); FAB MS 466 (M+H)+ ; 1H NMR (CDCl3) of α/β anomer, δ 8.12 (d, 1, 6-H), 7.7 (m, 4, ArH), 7.4 (m, 6, ArH), 6.32 (m, 1, 1'-H), 5.9-5.3 (hump, 1, NH2), 5.75 (d, 1, 5-H), 5.45 (d, 1, 5-H), 3.75 (m, 3, 4'-Hα,β 's, 3'-Hα,β 's).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05128458
출처 데이터셋uspto-grants-1992_07
ORD IDord-e369a01e7e4949d5a42ef03f07094859
출처 메모uspto-grants-1992_07