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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989241Generated: October 29, 2026

Ammonium Chloride → HCID 18005445, compound

https://huagongshe.com/reaction/989241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(Ethylsulfonyl)etheneHCID 74680—
ReactantPotassium hydrideHCID 82127—
ReactantHCID 10861895HCID 10861895—
SolventDimethylformamideHCID 6228—
ProductHCID 18005445HCID 1800544531.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a suspension of 35% potassium hydride in oil (0.7 g) in dry N,N-dimethylformamide (DMF) was added a solution of 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(methylsulfinyl)-1H-pyrazole-3-carbonitrile (10.0 g) in dry DMF dropwise at 4° C. over 10 minutes. After stirring for 20 minutes, vinyl ethyl sulfone (3.13 g) in dry DMF was added during 5 hours at 4° C. The mixture was stirred overnight under nitrogen with warming to 20° C. Ammonium chloride was added at 4° C., and the mixture extracted (ethyl acetate), washed twice with water, dried (sodium sulfate) and evaporated. Crystallization from ethyl acetate/methanol/hexane gave 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-[2-(ethylsulfonyl)ethylamino]-4-(methylsulfinyl)-1H-pyrazole-3-carbonitrile (4.08 g), m.p.131-132° C. By proceeding in a similar manner the following compounds were prepared:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638956B2
Source datasetuspto-grants-2003_10
ORD IDord-0adbf66a133a438da1bde4a173119796
Source noteuspto-grants-2003_10