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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420897Generated: October 31, 2026

1,3-Propanedithiol → 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(1,3-dithian-2-yl)-1H-pyrazole-3-carbonitrile

https://huagongshe.com/reaction/420897

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanedithiolHCID 8013—
ReactantSodium HydroxideHCID 14798—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-formylpyrazoleHCID 19356478—
SolventDichloromethaneHCID 6344—
Product5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(1,3-dithian-2-yl)-1H-pyrazole-3-carbonitrileHCID 2313191633%

Reaction Steps

To the solution of 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-formyl-1H-pyrazole-3-carbonitrile (0.5 g, 1.4 mmol) in dichloromethane (10 mL) was added N-bromosuccinimide (0.075 g, 0.2 mmol) followed by the addition of 1,3-dimercaptopropane (0.19 g, 1.8 mmol). The resulting solution was stirred at room temperature for eight hours. It was then worked-up by the addition of 2 N sodium hydroxide. The layers were separated and the organic layer was dried (Na2SO4) and concentrated. The resulting solid was further purified via silica gel column eluting with heptane:ethyl acetate (1:1) to afford a white solid (0.2 g, 33%). 19F-NMR: −64.231.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097732B2
Source datasetuspto-grants-2012_01
ORD IDord-c09af8d7191c4465b97c32d7fc432258
Source noteuspto-grants-2012_01