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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 441940생성일: 2026년 10월 25일

Ammonia → Medazepam

https://huagongshe.com/reaction/441940

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물DiazepamHCID 3016—
반응물Boron trifluoride etherateHCID 8000—
반응물Sodium borohydrideHCID 4311764—
용매TetrahydrofuranHCID 8028—
생성물MedazepamHCID 4041103%

반응 단계

To a suspension of 2.28 g of sodium borohydride in 35ml of tetrahydrofuran was added dropwise with stirring a solution of 13.0 g of boron trifluoride etherate in 10ml of tetrahydrofuran below 10° C, and the mixture was stirred at room temperature for 45 minutes. To the mixture was added dropwise solution of 1.43 g of 1-methyl-5-phenyl-7-chloro-1,3-dihydro-2H-1,4-benzodiazepin-2-one in 10 ml of tetrahydrofuran at -15° to -12.5° C over a period of 5 minutes, and then the mixture was stirred at =15° C for 22 hours. The reaction mixture was poured into 100 ml of ice-water, and then 20 ml of concentrated hydrochloric acid was added. The mixture was refluxed for 30 minutes, then cooled, and neutralized with concentrated ammonia. The tetrahydrofuran layer was separated, and the aqueous layer was extracted with ether. The combined organic layer was washed with water and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure to obtain 1.4 g of 1-methyl-5-phenyl-7-chloro-2,3-dihydro-1H-1,4-benzodiazepine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04044003
출처 데이터셋uspto-grants-1977_08
ORD IDord-f477172c64e844b98d04e50fc6afdfa7
출처 메모uspto-grants-1977_08