4-Nitrobenzaldehyde → HCID 67686873, compound

HRID 2284279Notes

Reaction equation

HRID 2284279 reaction equation
[C:1]1([C:7]2[CH:12]=[CH:11][C:10]([N+:13]([O-])=O)=[C:9]([N+:16]([O-])=O)[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N+:19]([C:22]1[CH:29]=[CH:28][C:25]([CH:26]=O)=[CH:24][CH:23]=1)([O-])=O.[NH:30]1[CH:34]=[CH:33][CH:32]=[C:31]1[C:35](O)=[O:36]>>[C:1]1([C:7]2[CH:12]=[CH:11][C:10]3[N:13]=[C:26]([C:25]4[CH:28]=[CH:29][C:22]([NH:19][C:35]([C:31]5[NH:30][CH:34]=[CH:33][CH:32]=5)=[O:36])=[CH:23][CH:24]=4)[NH:16][C:9]=3[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

4

Reactant 3

HCID 5414-NitrobenzaldehydeHCID 12473Pyrrole-2-Carboxylic AcidHCID 15052906HCID 15052906, compound

Product 1

HCID 67686873HCID 67686873, compound

Procedure

Compound 644 was prepared according to the procedure similar to that described in Scheme III from 1-phenyl-3,4-dinitrobenzene, 4-nitrobenzaldehyde, and 2-pyrrolecarboxylic acid. [M+H]+ calcd for C24H18N4O: 379.15; found: 378.96.

Sources & evidence

ORD record
ord-becfa8feaaf144f982811bec32150929
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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