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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371129Generated: October 29, 2026

1,2-Dichloro-4-isothiocyanatobenzene → N-(3,4-Dichlorophenyl)-4-[(1-methylpiperidin-3-yl)methyl]piperazine-1-carbothioamide

https://huagongshe.com/reaction/2371129

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dichloro-4-isothiocyanatobenzeneHCID 23065—
Reactant1-[(1-Methylpiperidin-3-yl)methyl]piperazineHCID 2736940—
ReactantSodium trimethylsilylamideHCID 23692414—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductN-(3,4-Dichlorophenyl)-4-[(1-methylpiperidin-3-yl)methyl]piperazine-1-carbothioamideHCID 57656911—

Reaction Steps

To a solution of 1-[(1-methylpiperidin-3-yl)methyl]piperazine (400 mg) in chloroform (10 ml) was added a 2M solution of sodium(trimethylsilyl)amide in THF (2.2 ml). The resulting solution was stirred at room temperature for 10 minutes. 3,4-Dichlorophenylisothiocyanate (0.44 ml) was added and mixture stirred at room temperature for 1 hour. The reaction was quench with water (1 ml) then concentrated in vacuo before being separated between ethyl acetate (100 ml) and saturated sodium bicarbonate solution (100 ml). The ethyl acetate layer was separated, dried over magnesium sulphate, filtered then concentrated in vacuo onto silica gel (1.0 g). The resulting powder was purified by column chromatography on silica gel (50 g) using a gradient of 100% dichloromethane through to 10% methanolic ammonia in dichloromethane to give the title compound (726 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710224B2
Source datasetuspto-grants-2014_04
ORD IDord-8d900e7e1e004285a3a99033bc66bdf8
Source noteuspto-grants-2014_04