戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 338125作成日:2026年10月25日

Sodium Bicarbonate → Racemic Benzyl 2-benzamido-7a-phenyl-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazine-6-carboxylate

https://huagongshe.com/reaction/338125

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物1-Chloro-N,N-2-trimethylpropenylamineHCID 640792—
反応物Benzyl 3-(benzoylcarbamothioylamino)-4-(hydroxymethyl)-3-phenyl-pyrrolidine-1-carboxylateHCID 86697917—
溶媒DichloromethaneHCID 6344—
生成物Racemic Benzyl 2-benzamido-7a-phenyl-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazine-6-carboxylateHCID 8983230263.2%

反応手順

1-Chloro-N,N,2-trimethylpropenylamine (17.9 mL, 135 mmol) is added to a 0° C. solution of racemic benzyl 3-(benzoylcarbamothioylamino)-4-(hydroxymethyl)-3-phenyl-pyrrolidine-1-carboxylate (51 g, 104 mmol) in dichloromethane (459 mL) and stirred at room temperature for 2 hours. A saturated solution of sodium hydrogen carbonate (300 mL) is added and the layers are separated. The organic layer is dried over magnesium sulfate, the solution concentrated. The crude product is purified over silica gel eluting with dichloromethane to 5% ethyl acetate/dichloromethane to give the title compound (31 g, 63%). ES/MS (m/e): 372 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889856B2
出典データセットuspto-grants-2014_11
ORD IDord-8a1aa82555384bd6a69ae9066207428b
出典メモuspto-grants-2014_11