4,4'-Diaminobenzophenone → HCID 67112941, compound

HRID 2284189Notes

Reaction equation

HRID 2284189 reaction equation
[NH2:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([NH2:14])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.[OH:17][CH2:18][CH2:19][N:20]([CH2:30][CH2:31][OH:32])[C:21]1[CH:29]=[CH:28][C:24]([C:25]([O-])=[O:26])=[CH:23][CH:22]=1>>[C:6]([C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:25](=[O:26])[C:24]2[CH:28]=[CH:29][C:21]([N:20]([CH2:30][CH2:31][OH:32])[CH2:19][CH2:18][OH:17])=[CH:22][CH:23]=2)=[CH:10][CH:9]=1)([C:5]1[CH:15]=[CH:16][C:2]([NH:1][C:25](=[O:26])[C:24]2[CH:28]=[CH:29][C:21]([N:20]([CH2:19][CH2:18][OH:17])[CH2:30][CH2:31][OH:32])=[CH:22][CH:23]=2)=[CH:3][CH:4]=1)=[O:7]

Participants

3

Procedure

Compound 327 was prepared according to the procedure described in Scheme IV from 4,4′-diaminobenzophenone and 4-bis(2-hydroxylethyl)aminobenzoate. [M+H]+ calcd for C35H38N4O7: 627.28; found: 627.06.

Sources & evidence

ORD record
ord-cc123b8c5f534306b41548bfea3f826a
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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