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HRID 441941作成日:2026年10月26日

Ammonia → 1-methyl-5-phenyl-7-nitro-2,3-dihydro-1H-1,4-benzodiazepine

https://huagongshe.com/reaction/441941

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Hydrochloric AcidHCID 313—
反応物NimetazepamHCID 4496—
反応物DiboronHCID 6328200—
溶媒TetrahydrofuranHCID 8028—
生成物1-methyl-5-phenyl-7-nitro-2,3-dihydro-1H-1,4-benzodiazepineHCID 2141604495%

反応条件

温度-8 °C

反応手順

To a solution of 30 ml of 1.07 M diborane in tetrahydrofuran was added with stirring 1.48 g of 1-methyl-5-phenyl-7-nitro-1,3-dihydro-2H-1,4-benzodiazepin-2-one at -13° to -8° C, and the mixture was further stirred at -8° C for 1 hour and 45 minutes. The reaction mixture was poured into ice-water, and 20 ml of concentrated hydrochloric acid was added. The mixture was refluxed for one hour. After cooling, the resultant solution was neutralized with 28%-aqueous ammonia, and extracted with chloroform. The chloroform extracts were washed with water and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was dissolved in a 20%-solution of hydrochloric acid in ethyl alcohol, and refluxed for 10 minutes. The alcohol was removed by distillation under reduced pressure, and the residue was distributed between water and chloroform. The chloroform layer was separated, washed with water, and dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to obtain 1.34 g of 1-methyl-5-phenyl-7-nitro-2,3-dihydro-1H-1,4-benzodiazepine, which was recrystallized from isopropyl alcohol to yield yellow flakes melting at 186° to 187° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04044003
出典データセットuspto-grants-1977_08
ORD IDord-566be60e615641caaeae75280a5c1186
出典メモuspto-grants-1977_08