2-Nitrobenzaldehyde → HCID 178439637, compound

HRID 489384Notes

Reaction equation

HRID 489384 reaction equation
[N+:1]([C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[CH:6]=O)([O-:3])=[O:2].[NH2:12][C:13]1[CH:17]=[CH:16][NH:15][N:14]=1>>[N+:1]([C:4]1[CH:6]([C:5]2[CH:8]=[CH:9][CH:10]=[CH:11][C:4]=2[N+:1]([O-:3])=[O:2])[C:17]2[C:13](=[N:14][NH:15][CH:16]=2)[NH:12][C:5]=1[CH2:8][CH2:9][CH3:10])([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 111012-NitrobenzaldehydeHCID 178418806HCID 178418806, compound

Product 1

HCID 178439637HCID 178439637, compound

Procedure

The title compound was prepared from n-butylaldehyde, 2-nitrobenzaldehyde and 3-aminopyrazole in the same manner as in Example 93.

Sources & evidence

ORD record
ord-c9af8e6baaac4c938fa0586170da5e65
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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