4-(4-Morpholinophenyl)aminocarbonylbenzaldehyde → 4-(6-(Pyridin-2-ylmethoxy)-1H-benzo[d]imidazol-2-yl)-N-(4-morpholinophenyl)benzamide

HRID 2284264Notes

Reaction equation

HRID 2284264 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[C:11]([N+:18]([O-])=O)[CH:10]=1.[O:21]1[CH2:26][CH2:25][N:24]([C:27]2[CH:32]=[CH:31][C:30]([NH:33][C:34]([C:36]3[CH:43]=[CH:42][C:39]([CH:40]=O)=[CH:38][CH:37]=3)=[O:35])=[CH:29][CH:28]=2)[CH2:23][CH2:22]1>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]2[N:15]=[C:40]([C:39]3[CH:38]=[CH:37][C:36]([C:34]([NH:33][C:30]4[CH:29]=[CH:28][C:27]([N:24]5[CH2:23][CH2:22][O:21][CH2:26][CH2:25]5)=[CH:32][CH:31]=4)=[O:35])=[CH:43][CH:42]=3)[NH:18][C:11]=2[CH:10]=1

Participants

3

Procedure

Compound 624 was prepared according to the procedure similar to that described in Scheme III from 1-(pyridin-2-ylmethoxy)-3,4-dinitrobenzene and 4-(4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C30H27N5O3: 506.21; found: 506.06.

Sources & evidence

ORD record
ord-4636bf89b2344f58a00ef8d5bfacdd2a
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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