Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250002Generated: October 26, 2026

6-Chloro-2-benzothiazolamine → N-(6-chlorobenzo[d]thiazol-2-yl)-1H-imidazole-1-carbothioamide

https://huagongshe.com/reaction/250002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-2-benzothiazolamineHCID 7226—
Reactant1,1'-ThiocarbonyldiimidazoleHCID 80264—
SolventAcetonitrileHCID 6342—
ProductN-(6-chlorobenzo[d]thiazol-2-yl)-1H-imidazole-1-carbothioamideHCID 5808796664%

Reaction Conditions

Temperature50 °C

Reaction Steps

To 6-chlorobenzo[d]thiazol-2-amine (1.14 g, 6.17 mmol) in acetonitrile (30 mL) was added 1,1′-thiocarbonyldiimidazole (1.43 g, 8 mmol). The reaction was stirred at 50° C. for 18 hours. The reaction was cooled to room temperature and the precipitate was filtered and washed with acetonitrile (2×50 mL). The yellow powder was dried in a vacuum oven (40° C.) for 1 hour to yield N-(6-chlorobenzo[d]thiazol-2-yl)-1H-imidazole-1-carbothioamide (1.16 g, 3.9 mmol, 64% yield) and then used in the next step without any further purification or characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863291B2
Source datasetuspto-grants-2011_01
ORD IDord-0afa20145a894ab9bd015045304d18b6
Source noteuspto-grants-2011_01