Acetic Anhydride → HCID 19390967, compound
Reaction equation
[NH2:1][C:2]1[N:3]([CH3:8])[N:4]=[CH:5][C:6]=1[Br:7].[C:9](OC(=O)C)(=[O:11])[CH3:10]>>[C:9]([NH:1][C:2]1[N:3]([CH3:8])[N:4]=[CH:5][C:6]=1[Br:7])(=[O:11])[CH3:10]Participants
3
Procedure
3-acetamido-4-bromo-2-methylpyrazole (92°-94° C.) was prepared by acetylation of 3-amino-4-bromo-2-methylpyrazole in acetic anhydride.
Sources & evidence
- ORD record
- ord-424c5783fca143489c71b656d8fdfad8
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05441969
Reaction notes
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