4,4'-Diaminobenzophenone → HCID 67686614, compound

HRID 2284186Notes

Reaction equation

HRID 2284186 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.[N:17]1([C:23]2[CH:31]=[CH:30][C:26]([C:27]([O-])=[O:28])=[CH:25][CH:24]=2)[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1>>[C:6]([C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:27](=[O:28])[C:26]2[CH:30]=[CH:31][C:23]([N:17]3[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]3)=[CH:24][CH:25]=2)=[CH:10][CH:9]=1)([C:5]1[CH:15]=[CH:16][C:2]([NH:1][C:27](=[O:28])[C:26]2[CH:30]=[CH:31][C:23]([N:17]3[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]3)=[CH:24][CH:25]=2)=[CH:3][CH:4]=1)=[O:7]

Participants

3

Reactant 2

HCID 691494,4'-DiaminobenzophenoneHCID 34381734-(Piperidin-1-yl)benzoate

Product 1

HCID 67686614HCID 67686614, compound

Procedure

Compound 322 was prepared according to the procedure described in Scheme IV from 4,4′-diaminobenzophenone and 4-piperidinobenzoate. [M+H]+ calcd for C37H38N4O3: 587.30; found: 587.02.

Sources & evidence

ORD record
ord-77c6d0a57dcf4630848620f0e02907e8
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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