Ammonium Chloride → 1-Methyl-4-nitro-1H-pyrazole-3-carboxamide
Reaction equation
[CH3:1][N:2]1[CH:6]=[C:5]([N+:7]([O-:9])=[O:8])[C:4]([C:10]([OH:12])=O)=[N:3]1.[Cl-].[NH4+:14]>>[CH3:1][N:2]1[CH:6]=[C:5]([N+:7]([O-:9])=[O:8])[C:4]([C:10]([NH2:14])=[O:12])=[N:3]1Participants
3
Procedure
The product was obtained according to the method described in example 1, step 1 starting from 1-methyl-4-nitro-1H-pyrazole-3-carboxylic acid and two equivalents of ammonium chloride as amine source as light yellow solid (110 mg, 37%).
Workup
- customThe product was obtained
Sources & evidence
- ORD record
- ord-bf9c17c59c834af988fb241cdbb12ba1
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08623866B2
Reaction notes
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