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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Clonazepam | HCID 2802 | — |
| 반응물 | Ethylene Oxide | HCID 6354 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 11b-(2-chlorophenyl)-10-nitro-2,3,5,11b-tetrahydrooxazolo[3,2-d][1,4]benzodiazepin-6(7H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03965151 |
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| 출처 데이터셋 | uspto-grants-1976_06 |
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| ORD ID | ord-04f15e6fd4774174ad1ae4a2134a164d |
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| 출처 메모 | uspto-grants-1976_06 |
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