Ammonia → HCID 54565766, compound
Reaction equation
[F:1][CH:2]([F:19])[O:3][C:4]1[N:8]([CH3:9])[N:7]=[C:6]([N:10]2[C:14]([CH3:15])=[C:13]([C:16](Cl)=[O:17])[CH:12]=[N:11]2)[CH:5]=1.[NH3:20]>O1CCCC1>[F:1][CH:2]([F:19])[O:3][C:4]1[N:8]([CH3:9])[N:7]=[C:6]([N:10]2[C:14]([CH3:15])=[C:13]([C:16]([NH2:20])=[O:17])[CH:12]=[N:11]2)[CH:5]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.98 g (3.38 mmol) 1-(5-Difluoromethoxy-1-methyl-3-pyrazolyl)-5-methyl-4-pyrazolecarbonyl chloride was dissolved in 20 ml tetrahydrofuran and 50 ml aqueous ammonia (33%) was added with stirring. After stirring for 3 hours at room temperature, the mixture was concentrated to half and acidified with dilute hydrochloric acid. The precipitate was suction filtered off, washed with a small amount of water and dried.
Workup
- stirringAfter stirring for 3 hours at room temperature
- concentrationthe mixture was concentrated to half
- filtrationfiltered off
- washwashed with a small amount of water
- customdried
Sources & evidence
- ORD record
- ord-ab5b4dde538945b9896e7df58011de47
- Source dataset
- uspto-grants-1999_02
- Patent number
- US05869686
Reaction notes
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