Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131421생성일: 2026년 10월 25일
Diisopropylethylamine → (S)-7-fluoro-2-trifluoromethyl-11-[3-(3-methoxy-propyl)-piperazin 1-yl]-5H-dibenzo[b,e][1,4]diazepine
https://huagongshe.com/reaction/131421
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | (2S)-2-(3-Methoxypropyl)piperazine | HCID 45099475 | — |
| 반응물 | 7-Fluoro-2-trifluoromethyl-5H-dibenzo[b,e][1,4]diazepin-11-ylamine hydrochloride | HCID 69210778 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | (S)-7-fluoro-2-trifluoromethyl-11-[3-(3-methoxy-propyl)-piperazin 1-yl]-5H-dibenzo[b,e][1,4]diazepine | HCID 10388301 | 51.2% |
반응 단계
Combine 7-fluoro-2-trifluoromethyl-5H-dibenzo[b,e][1,4]diazepin-11-ylamine hydrochloride (0.399 g, 1.20 mmol), (S)-2-(3-methoxy-propyl)-piperazine (0.381 g, 2.41 mmol), and diisopropylethyl amine (0.21 mL, 1.20 mmol) in a mixture of toluene (4.5 mL) and dimethylsulfoxide (1.5 mL) and stir at 110° C. for 24 hours. Evaporate the mixture then purify by flash chromatography, eluting with a step gradient starting with dichloromethane going to 7% 2N ammonia-methanol in dichloromethane gives (s)-7-fluoro-11-[3-(3-methoxy-propyl)-piperazin-1-yl]-2-trifluoromethyl-5H-dibenzo[b,e][1,4]diazepine (0.268 g, 0.614 mmol, 51%) as a yellow oil. Mass spectrum (APCI): m/z=437.2 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07384934B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-e5e879f3567541a2bb3418a896305506 |
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| 출처 메모 | uspto-grants-2008_06 |
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