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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494287생성일: 2026년 10월 25일

(1,1'-Biphenyl)-4-carboxylic acid → N-(1-Methylisoquinolin-5-yl)-1,1'-biphenyl-4-carboxamide

https://huagongshe.com/reaction/494287

반응식

참여 물질

역할이름HCID투입량
반응물(1,1'-Biphenyl)-4-carboxylic acidHCID 66724—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Methylisoquinolin-5-amineHCID 9989490—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물N-(1-Methylisoquinolin-5-yl)-1,1'-biphenyl-4-carboxamideHCID 57682685—

반응 조건

온도38 °C

반응 단계

To a solution of 1-methyl-5-aminoisoquinoline (94 (75 mg, 0.47 mmol) in DCM (4 ml) was added 4-biphenylcarboxylic acid (141 mg, 0.71 mmol), 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride (135 mg, 0.71 mmol) and 4-dimethylaminopyridine (10 mg, 0.08 mmol) and the reaction stirred at 38° C. for 3 days. The mixture was diluted with DCM, washed with sat. aqueous sodium bicarbonate solution and water, dried over MgSO4 and concentrated in vacuo to give the crude product which was triturated with methanol. The resulting precipitate was collected by filtration, washed with ether and dried in vacuo giving the title compound as an off-white solid. 1H NMR (400 MHz, CDCl3) δ (ppm): 8.48 (d, 1H), 8.33 (d, 1H), 8.21 (br, 1H), 8.06 (m, 3H), 7.78 (d, 2H), 7.68 (m, 3H), 7.58 (d, 1H), 7.51 (t, 2H), 7.41 (t, 1H), 3.02 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538121B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-14027445796e482cb578d89752b33991
출처 메모uspto-grants-2009_05