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HRID 1389808作成日:2026年10月27日

Water → 3-Fluoro-1,3-dihydro-1-methyl-7-chloro-5-phenyl-2H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/1389808

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TemazepamHCID 5391—
反応物(Diethylamino)sulfur trifluorideHCID 123472—
溶媒DichloromethaneHCID 6344—
生成物3-Fluoro-1,3-dihydro-1-methyl-7-chloro-5-phenyl-2H-1,4-benzodiazepin-2-oneHCID 1260212070%

反応手順

A solution of 12.1 g (0.04 mol) of 3-hydroxy-1,3-dihydro-1-methyl-7-chloro-5-phenyl-2H-1,4-benzodiazepin-2-one in 25 ml of anhydrous methylene chloride was added dropwise over a period of 15 min. to a stirred solution of 12.6 ml (0.1 mol) of diethylaminosulfur trifluoride in 300 ml of anhydrous methylene chloride cooled to -70° . The reaction mixture was allowed to warm slowly over a period of 45 min. to 5° and then poured into 500 ml of ice and water. The lower organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and evaporated to drynes under reduced pressure to give 10.9 g (90% yield) of crude product as a light yellow solid residue. Recrystallization from heptane gave 8.48 g (70% yield) of 3-fluoro-1,3-dihydro-1-methyl-7-chloro-5-phenyl-2H-1,4-benzodiazepin-2-one as colorless crystals: mp 138°-140°; 19F nmr (CCl3D) δ -161.7 ppm (d, J=57 Hz); 1H nmr (CCl3D) δ 3.43 ppm (s, 3H), 5.54 ppm (d, J=57 Hz, 1H), 7.5 ppm (m, 8H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04246270
出典データセットuspto-grants-1981_01
ORD IDord-4a982f79934d4c26971afc58555f3c2f
出典メモuspto-grants-1981_01