Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diazepam → 10-chloro-2-chloromethyl-2,3,5,11b-tetrahydro-7-methyl-11b-phenyloxazolo[3,2-d][1,4]benzodiazepin-6(7H)-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diazepam | HCID 3016 | — |
| 반응물 | Epichlorohydrin | HCID 7835 | — |
| 반응물 | Aluminum(III) Chloride | HCID 6451240 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 10-chloro-2-chloromethyl-2,3,5,11b-tetrahydro-7-methyl-11b-phenyloxazolo[3,2-d][1,4]benzodiazepin-6(7H)-one | HCID 21409971 | — |
반응 단계
A mixture of 10 g. (35 mmole) of 7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one, 10 g. of aluminum chloride, and 200 ml. of dried benzene was treated with 30 ml. of 1-chloro-2,3-epoxypropane in 100 ml. of benzene. The reaction mixture was stirred overnight. Work-up as in Method A, Example 5, above gave 32 g. of a crude oil. The oil was dissolved in benzene, filtered over Florisil, evaporated to dryness and crystallized from ether-petroleum ether to give the above-titled product as colorless needles, m.p. 140°-142°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04049666 |
| 출처 데이터셋 | uspto-grants-1977_09 |
| ORD ID | ord-a743c854d4464ceab17d8cd01a7e8779 |
| 출처 메모 | uspto-grants-1977_09 |