3,3'-Diaminobenzidine → HCID 178419856, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:15]=[CH:14][C:12]([NH2:13])=[C:11]([NH2:16])[CH:10]=2)[CH:5]=[CH:6][C:7]=1[NH2:8].[N:17]1([C:23]2[CH:30]=[CH:29][C:26]([CH:27]=O)=[CH:25][CH:24]=2)[CH2:22][CH2:21][O:20][CH2:19][CH2:18]1>>[NH:8]1[C:7]2[CH:6]=[CH:5][C:4]([C:9]3[CH:15]=[CH:14][C:12]4[N:13]=[C:27]([C:26]5[CH:29]=[CH:30][C:23]([N:17]6[CH2:22][CH2:21][O:20][CH2:19][CH2:18]6)=[CH:24][CH:25]=5)[NH:16][C:11]=4[CH:10]=3)=[CH:3][C:2]=2[N:1]=[C:27]1[C:26]1[CH:25]=[CH:24][C:23]([N:17]2[CH2:22][CH2:21][O:20][CH2:19][CH2:18]2)=[CH:30][CH:29]=1Participants
3
Procedure
Compound 286 was prepared according to the procedure similar to that described in Scheme III from 3,3′-diaminobenzidine and 4-morpholinylbenzaldehyde. [M+H]+ calcd for C34H32N6O2: 557.26; found: 557.58.
Sources & evidence
- ORD record
- ord-ea84aeb5bf1f4ba6b07edd638befa908
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
Loading…