2-Nitrobenzaldehyde → HCID 178509368, compound

HRID 489415Notes

Reaction equation

HRID 489415 reaction equation
[CH:1]1([C:4](OC)=O)C[CH2:2]1.[N+:8]([C:11]1[CH:18]=[CH:17][CH:16]=[CH:15][C:12]=1[CH:13]=O)([O-:10])=[O:9].[NH2:19][C:20]1[CH:24]=[CH:23][NH:22][N:21]=1>>[C:11]([C:12]1[CH:13]([C:12]2[CH:15]=[CH:16][CH:17]=[CH:18][C:11]=2[N+:8]([O-:10])=[O:9])[C:24]2[C:20](=[N:21][NH:22][CH:23]=2)[NH:19][C:13]=1[CH:4]1[CH2:1][CH2:2]1)#[N:8]

Participants

4

Reactant 3

HCID 111012-NitrobenzaldehydeHCID 76122Methyl cyclopropanecarboxylateHCID 178418806HCID 178418806, compound

Product 1

HCID 178509368HCID 178509368, compound

Procedure

The title compound was prepared from methyl cyclopropanecarboxylate, 2-nitrobenzaldehyde and 3-aminopyrazole in the same manner as in Example 94.

Sources & evidence

ORD record
ord-6c30f43ce30c45d687431d621de74f0f
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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