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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252870Generated: October 30, 2026

Dichloromethane → 4-(4-Cyanobenzyl)piperazine-1-carbothioamide

https://huagongshe.com/reaction/252870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
Reactant1-Boc-4-(4-Cyanobenzyl)piperazineHCID 18382257—
SolventMethanolHCID 887—
SolventTrifluoroacetic acidHCID 6422—
Product4-(4-Cyanobenzyl)piperazine-1-carbothioamideHCID 8604043750%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of tert-butyl 4-(4-cyanobenzyl)piperazine-1-carboxylate (336, 1.374 g, 4.56 mmol) in DCM (5 mL) and TFA (5 mL) was stirred at room temperature for one hour. The reaction mixture was concentrated and the residue was added to a solution of thiocarbonyldiimidazole (1.21 g, 6.84 mmol, 1.5 equiv.) in dry DCM (20 mL) under N2 at 0° C. Obtained solid was diluted with MeOH (20 mL) and transferred to a pressure vial. Ammonia gas was bubbled in for 10 min and the flask was capped and stirred at 80° C. for two days. The reaction mixture was concentrated and purified by flash chromatography using 60% EtOAc in hexane as an eluent, to afford the title compound 337 (593 mg, 50% yield). MS: calc: 260.1; found: 261.2 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868205B2
Source datasetuspto-grants-2011_01
ORD IDord-903b24d46f9d4024862180afb5f5ca09
Source noteuspto-grants-2011_01