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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

반응식

참여 물질

역할이름HCID투입량
반응물Bromodifluoromethyl diethylphosphonateHCID 144101—
반응물N-(7-hydroxyisoquinolin-3-yl)cyclopropanecarboxamideHCID 67975011—
용매Ethyl AcetateHCID 8857—
용매Acetonitrile--water (1/1)HCID 18373917—
생성물N-(7-(Difluoromethoxy)isoquinolin-3-yl)cyclopropanecarboxamideHCID 6797673338.5%

반응 조건

온도-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623889B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-aef7cf60683146efa12c723ea2853134
출처 메모uspto-grants-2014_01