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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420895Generated: October 30, 2026

Sodium borohydride → 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(1,3-dithiolan-2-yl)-5-(methylamino)-1H-pyrazole-3-carbonitrile

https://huagongshe.com/reaction/420895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(1,3-dithiolan-2-yl)-1H-pyrazole-3-carbonitrile ethoxyethyleneHCID 86620473—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(1,3-dithiolan-2-yl)-5-(methylamino)-1H-pyrazole-3-carbonitrileHCID 23131915100%

Reaction Steps

To the solution of 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(1,3-dithiolan-2-yl)-1H-pyrazole-3-carbonitrile-ethoxyethylene (1:1) (0.30 g, 0.6 mmol) in ethanol (40 mL) at 5 C was added sodium borohydride (74 mg, 1.9 mmol). The resulting mixture was stirred at room temperature for five hrs and then diluted with water and ethyl acetate. The layers were separated and the organic layer was washed with saturated sodium chloride, dried (Na2SO4), concentrated to afford a yellowish oil (0.27 g, 0.6 mmol); 19-F-NMR: −63.704.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097732B2
Source datasetuspto-grants-2012_01
ORD IDord-455c3442e3a44b99909c39b71e599e11
Source noteuspto-grants-2012_01