Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 468800생성일: 2026년 10월 25일
Bromodifluoromethyl diethylphosphonate → N-(7-(Difluoromethoxy)isoquinolin-3-yl)cyclopropanecarboxamide
https://huagongshe.com/reaction/468800
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromodifluoromethyl diethylphosphonate | HCID 144101 | — |
| 반응물 | N-(7-hydroxyisoquinolin-3-yl)cyclopropanecarboxamide | HCID 67975011 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Acetonitrile--water (1/1) | HCID 18373917 | — |
| 생성물 | N-(7-(Difluoromethoxy)isoquinolin-3-yl)cyclopropanecarboxamide | HCID 67976733 | 38.5% |
반응 단계
A solution of N-(7-hydroxyisoquinolin-3-yl)cyclopropanecarboxamide (91.2 mg, 0.40 mmol), diethyl bromodifluoromethylphosphonate (212 mg, 0.80 mmol) in acetonitrile/water (1:1, 5 mL) was mixed and stirred at −78° C. After the reaction mixture was warmed to room temperature and stirred for 20 minutes, the reaction mixture was diluted with ethyl acetate, and the organic phase was separated. The water phase was extracted with ethyl acetate, and the combined organic layer was dried, concentrated and purified by prep-HPLC to give product (42.8 mg, 26%). LCMS (ESI): RT (min)=0.994, M+H+=279.0, method=A. 1H NMR (400 MHz, DMSO-d6) δ 8.92 (s, 1H), 8.54 (s, 1H), 8.37 (s, 1H), 7.79 (d, J=8.8 Hz, 1H), 7.54 (s, 1H), 7.43 (dd, J=2.4, 8.8 Hz, 1H), 6.61 (t, J=73.2 Hz, 1H), 1.71-1.57 (m, 1H), 1.15-1.11 (m, 2H), 0.95-0.89 (m, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08623889B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-aef7cf60683146efa12c723ea2853134 |
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| 출처 메모 | uspto-grants-2014_01 |
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