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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750342Generated: October 30, 2026

Lawesson's reagent → 1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carbothioamide

https://huagongshe.com/reaction/1750342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carboxamideHCID 86721179—
SolventTetrahydrofuranHCID 8028—
Product1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carbothioamideHCID 8672118065%

Reaction Steps

A solution of the compound (4.00 g, 15.31 mmol) obtained in step 3 and Lawesson's reagent (6.19 g, 15.31 mmol) in THF (50 mL) was stirred at 50° C. for 1.5 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by NH-silica gel column chromatography (solvent gradient; 2→65% ethyl acetate/hexane) to give 1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carbothioamide (2.75 g, 9.91 mmol, 65%) as a pale-yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156837B2
Source datasetuspto-grants-2015_10
ORD IDord-39e1fccf05b149bf8d12a9fcce7ee535
Source noteuspto-grants-2015_10