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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 468796생성일: 2026년 10월 25일

Phenol → N-(7-phenoxyisoquinolin-3-yl)cyclopropanecarboxamide

https://huagongshe.com/reaction/468796

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물Cesium carbonateHCID 10796—
반응물3,4,7,8-Tetramethyl-1,10-phenanthrolineHCID 74265—
반응물N-(7-bromoisoquinolin-3-yl)cyclopropanecarboxamideHCID 67974626—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DichloromethaneHCID 6344—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물N-(7-phenoxyisoquinolin-3-yl)cyclopropanecarboxamideHCID 6797508032.9%

반응 단계

N-(7-bromoisoquinolin-3-yl)cyclopropanecarboxamide (89 mg, 0.30 mmol), phenol (86.5 mg, 0.92 mmol, 3 eq), 3, 4,7,8-tetramethyl-1,10-phenanthrolin (35.4 mg, 0.15 mmol, 0.5 eq), copper(I) iodide (57.3 mg, 0.3 mmol, 1 eq) and cesium carbonate (293.2 mg, 0.9 mmol, 3 eq) in 1-methyl-2-pyrrolidinone (2.5 ml) were stirred under microwave irradiation at 180° C. for 99 min under nitrogen. The mixture was diluted with dichloromethane and filtered through a pad of Celite. The filer cake was washed with dichloromethane and the combined filtrate was concentrated and purified by prep-HPLC to give product (30 mg, 26%). LCMS (ESI): RT (min)=1.107, M+H+=305.0, method=A. 1H NMR (400 MHz, CDCl3) δ 8.76 (s, 1H), 8.46 (s, 1H), 8.24 (s, 1H), 7.72 (d, J=9.2 Hz, 1H), 7.38-7.00 (m, 5H), 1.55-1.52 (m, 1H), 1.10-1.06 (m, 2H), 0.87-0.82 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623889B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-5958112bbeeb487b926dbf700165028a
출처 메모uspto-grants-2014_01