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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1658608생성일: 2026년 10월 24일

Clonazepam → 11b-(2-chlorophenyl)-10-nitro-2,3,5,11b-tetrahydrooxazolo[3,2-d][1,4]benzodiazepin-6(7H)-one

https://huagongshe.com/ko/reaction/1658608

반응식

참여 물질

역할이름HCID투입량
반응물ClonazepamHCID 2802—
반응물Ethylene OxideHCID 6354—
반응물Ammonium HydroxideHCID 14923—
용매1,2-DichloroethaneHCID 11—
생성물11b-(2-chlorophenyl)-10-nitro-2,3,5,11b-tetrahydrooxazolo[3,2-d][1,4]benzodiazepin-6(7H)-oneHCID 12317902—

반응 단계

A solution of 5.2 g of (0.02 M) of stannic chloride in 60 ml of dry ethylene dichloride under nitrogen was treated with 2.9 g (0.0091 M) of 5-(2-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. The reaction was cooled in an ice bath, and 2.6 g (0.06 M) of ethylene oxide in 10 ml of ethylene dichloride was added with stirring over an 8 min period. After 18 hr at room temperature, the solution was made basic with concentrated ammonium hydroxide and filtered. The filtrates were washed with a saturated solution of brine, dried over anhydrous sodium sulfate and evaporated to dryness. The residue was crystallized from a mixture of dichloromethane, methanol and petroleum ether to give the above named product as white rods, melting at 201°-203°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03965151
출처 데이터셋uspto-grants-1976_06
ORD IDord-04f15e6fd4774174ad1ae4a2134a164d
출처 메모uspto-grants-1976_06