HCID 19348067, compound → HCID 178522192, compound

HRID 2284274Notes

Reaction equation

HRID 2284274 reaction equation
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:15]=[CH:14][C:13]([N+:16]([O-])=O)=[C:12]([N+:19]([O-])=O)[CH:11]=1.[O:22]1[CH2:27][CH2:26][N:25]([C:28]2[CH:33]=[CH:32][C:31]([NH:34][C:35]([C:37]3[CH:44]=[CH:43][C:40]([CH:41]=O)=[CH:39][CH:38]=3)=[O:36])=[CH:30][CH:29]=2)[CH2:24][CH2:23]1>>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:15]=[CH:14][C:13]2[NH:16][C:41]([C:40]3[CH:39]=[CH:38][C:37]([C:35]([NH:34][C:31]4[CH:30]=[CH:29][C:28]([N:25]5[CH2:24][CH2:23][O:22][CH2:27][CH2:26]5)=[CH:33][CH:32]=4)=[O:36])=[CH:44][CH:43]=3)=[N:19][C:12]=2[CH:11]=1

Participants

3

Procedure

Compound 638 was prepared according to the procedure similar to that described in Scheme III from 1-(benzothiazol-2-yl)-3,4-dinitrobenzene and 4-(4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C31H25N5O2S: 532.18; found: 532.07.

Sources & evidence

ORD record
ord-ff20a4957fb143c287c6361364d71d13
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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