2-Chlorobenzothiazole → HCID 71486684, compound

HRID 284111Notes

Reaction equation

HRID 284111 reaction equation
[CH3:40][N:41]1[CH2:42][CH2:43][CH2:44][C:45]1=[O:46].[CH:21]([N:22]([CH2:23][CH3:24])[CH:25]([CH3:26])[CH3:27])([CH3:28])[CH3:29].[Cl:30][c:31]1[s:32][c:33]2[c:34]([n:35]1)[cH:36][cH:37][cH:38][cH:39]2.[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:31]1[s:32][c:33]2[c:34]([n:35]1)[cH:36][cH:37][cH:38][cH:39]2

Participants

5

Reactant 4

HCID 119872-ChlorobenzothiazoleHCID 13387N-methyl-2-pyrrolidoneHCID 81531DiisopropylethylamineHCID 712083983-(aminomethyl)-7-chloro-1-phenylquinolin-4(1H)-one

Product 1

HCID 71486684HCID 71486684, compound

Sources & evidence

ORD record
ord-00ed996d5b1c4288bff3d3e9463eb885
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

Loading…