Bromine → HCID 54167733, compound
Reaction equation
[NH2:1][C:2]1[N:6]([C:7]2[CH:11]=[C:10]([O:12][CH:13]([F:15])[F:14])[N:9]([CH3:16])[N:8]=2)[N:5]=[CH:4][C:3]=1[C:17]#[N:18].[Br:19]Br>C(O)(=O)C>[NH2:1][C:2]1[N:6]([C:7]2[C:11]([Br:19])=[C:10]([O:12][CH:13]([F:14])[F:15])[N:9]([CH3:16])[N:8]=2)[N:5]=[CH:4][C:3]=1[C:17]#[N:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5.0 g (20 mmol) 5-Amino-1-(5-difluoromethoxy-1-methyl-3-pyrazolyl)-4-pyrazolecarbonitrile was dissolved in 80 ml acetic acid. At room temperature, 1.2 ml (23 mmol) bromine was added, dropwise. After stirring for 15 minutes, the mixture was concentrated and stirred with diisopropyl ether/propanol. The solid material was suction filtered and dried.
Workup
- concentrationthe mixture was concentrated
- stirringstirred with diisopropyl ether/propanol
- filtrationfiltered
- customdried
Sources & evidence
- ORD record
- ord-56a21fe2798e43f09a611ad7756d5dfb
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05756424
Reaction notes
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