Triethylamine → 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)-phenyl]-4-methylsulfinyl-1H-pyrazole-3-carboxaldehyde oxime
Reaction equation
[NH2:1][C:2]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([C:14]([F:17])([F:16])[F:15])=[CH:9][C:8]=2[Cl:18])[N:5]=[C:4]([C:19]#[N:20])[C:3]=1[S:21]([CH3:23])=[O:22].Cl.CN[OH:27].C(N(CC)CC)C>CO>[NH2:1][C:2]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([C:14]([F:15])([F:16])[F:17])=[CH:9][C:8]=2[Cl:18])[N:5]=[C:4]([CH:19]=[N:20][OH:27])[C:3]=1[S:21]([CH3:23])=[O:22]Participants
5
Procedure
A mixture of 5-amino-3-cyano 1-[2,6-dichloro-4-(trifluoromethyl) phenyl]-4-methylsulfinyl-1H-pyrazole (1g), methylhydroxylamine hydrochloride (0.26g) and triethylamine (0.4g) was stirred in methanol at ambient temperature for 2 hours, evaporated, washed (water) extracted with ethyl acetate to give 5-amino- 1-[2,6-dichloro4-(trifluoromethyl)phenyl]-4-methylsulfinyl-1H-pyrazole-3-carboxaldehyde oxime (0.35g) as a white solid m.p. about 190° C.
Workup
- customevaporated
- washwashed (water)
- extractionextracted with ethyl acetate
Sources & evidence
- ORD record
- ord-ad176733efc841a39b21db0db03683b1
- Source dataset
- uspto-grants-1999_11
- Patent number
- US05981565
Reaction notes
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