1-(6-Bromo-4-chloroquinolin-3-YL)ethanone → 1-(6-bromo-4-((1-(dimethylamino)-2,3-dihydro-1H-inden-5-yl)amino)quinolin-3-yl)ethanone

HRID 2271548노트

반응식

HRID 2271548 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6]([C:12](=[O:14])[CH3:13])=[C:5]2Cl.Cl.Cl.[CH3:18][N:19]([CH3:30])[CH:20]1[C:28]2[C:23](=[CH:24][C:25]([NH2:29])=[CH:26][CH:27]=2)[CH2:22][CH2:21]1>>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6]([C:12](=[O:14])[CH3:13])=[C:5]2[NH:29][C:25]1[CH:24]=[C:23]2[C:28](=[CH:27][CH:26]=1)[CH:20]([N:19]([CH3:30])[CH3:18])[CH2:21][CH2:22]2

참가 물질

3

실험 절차

Following general procedure C, 1-(6-bromo-4-chloroquinolin-3-yl)ethanone (256 mg, 0.90 mmol) was reacted with N1,N1-dimethyl-2,3-dihydro-1H-indene-1,5-diamine dihydrochloride (0.814 mmol) to afford the desired product (19 mg, 5.5%) as a yellow-brown solid. ESI MS m/z 424 [C22H22BrN3O+H]+

출처 및 근거

ORD 기록
ord-32ca9e27994842a5baa005e3a194d4b5
출처 데이터셋
uspto-grants-2015_09
특허 번호
US09120749B2

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