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HRID 653981作成日:2026年10月27日

Chlorotrimethylsilane → HCID 15126108、化合物

https://huagongshe.com/reaction/653981

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物HexamethyldisilazaneHCID 13838—
反応物Sodium BicarbonateHCID 516892—
反応物1-O-Acetyl-5-O-t-butyldiphenylsilyl-4-thio-2,3-dideoxyribofuranoseHCID 15126098—
反応物Potassium perfluorobutanesulfonateHCID 23675274—
反応物CytosineHCID 178418229—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物HCID 15126108HCID 15126108—

反応条件

温度25 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05128458
出典データセットuspto-grants-1992_07
ORD IDord-e369a01e7e4949d5a42ef03f07094859
出典メモuspto-grants-1992_07