4-Dimethylaminobenzoate → N-(2-Acetyl-1-(4-(4-dimethylaminobenzamido)phenyl)-1H-indol-5-yl)-4-dimethylaminobenzamide

HRID 2284195Notes

Reaction equation

[C:1]([C:4]1[N:5]([C:14]2[CH:19]=[CH:18][C:17]([NH2:20])=[CH:16][CH:15]=2)[C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([NH2:13])=[CH:8][CH:7]=2)(=[O:3])[CH3:2].[CH3:21][N:22]([CH3:32])[C:23]1[CH:31]=[CH:30][C:26]([C:27]([O-])=[O:28])=[CH:25][CH:24]=1>>[C:1]([C:4]1[N:5]([C:14]2[CH:19]=[CH:18][C:17]([NH:20][C:27](=[O:28])[C:26]3[CH:30]=[CH:31][C:23]([N:22]([CH3:32])[CH3:21])=[CH:24][CH:25]=3)=[CH:16][CH:15]=2)[C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([NH:13][C:27](=[O:28])[C:26]1[CH:25]=[CH:24][C:23]([N:22]([CH3:21])[CH3:32])=[CH:31][CH:30]=1)=[CH:8][CH:7]=2)(=[O:3])[CH3:2]

Participants

Reactant 2

HCID 69502454-Dimethylaminobenzoate

HCID 866739852-Acetyl-5-amino-1-(4-aminophenyl)indole

Product 1

HCID 67112579N-(2-Acetyl-1-(4-(4-dimethylaminobenzamido)phenyl)-1H-indol-5-yl)-4-dimethylaminobenzamide

Procedure

Compound 372 was prepared according to the procedure described in Scheme IV from 2-acetyl-5-amino-1-(4-aminophenyl)indole and 4-dimethylaminobenzoate. [M+H]+ calcd for C34H33N5O3: 560.26; found: 560.02.

Sources & evidence

ORD record: ord-5b519675f3064ad0b084810643c59034
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

Loading…