3-(aminomethyl)-7-chloro-1-phenylquinolin-4(1H)-one → HCID 71217342, 화합물

반응식

[Cl:21][c:22]1[cH:23][cH:24][c:25]([CH2:26][n:27]2[c:28](=[O:36])[cH:29][c:30]([C:33](=[O:34])[OH:35])[cH:31][cH:32]2)[cH:37][cH:38]1.[NH2:1][CH2:2][c:3]1[cH:4][n:5](-[c:15]2[cH:16][cH:17][cH:18][cH:19][cH:20]2)[c:6]2[cH:7][c:8]([Cl:14])[cH:9][cH:10][c:11]2[c:12]1=[O:13]>>[NH:1]([CH2:2][c:3]1[cH:4][n:5](-[c:15]2[cH:16][cH:17][cH:18][cH:19][cH:20]2)[c:6]2[cH:7][c:8]([Cl:14])[cH:9][cH:10][c:11]2[c:12]1=[O:13])[C:33]([c:30]1[cH:29][c:28](=[O:36])[n:27]([CH2:26][c:25]2[cH:24][cH:23][c:22]([Cl:21])[cH:38][cH:37]2)[cH:32][cH:31]1)=[O:34]

참가 물질

반응물 2

HCID 712083983-(aminomethyl)-7-chloro-1-phenylquinolin-4(1H)-one

HCID 71208950HCID 71208950, 화합물

생성물 1

HCID 71217342HCID 71217342, 화합물

출처 및 근거

ORD 기록: ord-2fd0ca89b8f94b4a868d589584279d0f
출처 데이터셋: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D

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