4-Nitrobenzaldehyde → HCID 178526535, compound

HRID 2218355Notes

Reaction equation

HRID 2218355 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH2:9])[C:5]([NH2:8])=[N:6][CH:7]=1.[N+:10]([C:13]1[CH:20]=[CH:19][C:16]([CH:17]=O)=[CH:15][CH:14]=1)([O-:12])=[O:11]>>[Br:1][C:2]1[CH:3]=[C:4]2[N:9]=[C:17]([C:16]3[CH:19]=[CH:20][C:13]([N+:10]([O-:12])=[O:11])=[CH:14][CH:15]=3)[NH:8][C:5]2=[N:6][CH:7]=1

Participants

3

Reactant 2

HCID 5414-NitrobenzaldehydeHCID 6911565-Bromopyridine-2,3-diamine

Product 1

HCID 178526535HCID 178526535, compound

Procedure

The title compound was prepared from 5-bromo-2,3-diaminopyridine (0.94 g, 5 mmol) and 4-nitrobenzaldehyde (0.76 g, 5 mmol).

Sources & evidence

ORD record
ord-34436a2af99a4f1d8ef2ea62af5291f0
Source dataset
uspto-grants-2008_08
Patent number
US07410966B2

Reaction notes

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