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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 441941생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/441941

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물NimetazepamHCID 4496—
반응물DiboronHCID 6328200—
용매TetrahydrofuranHCID 8028—
생성물1-methyl-5-phenyl-7-nitro-2,3-dihydro-1H-1,4-benzodiazepineHCID 2141604495%

반응 조건

온도-8 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04044003
출처 데이터셋uspto-grants-1977_08
ORD IDord-566be60e615641caaeae75280a5c1186
출처 메모uspto-grants-1977_08