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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926406Generated: November 2, 2026

4-Amino-3-chlorobenzonitrile → 2-Chloro-1,3-benzothiazole-6-carbonitrile

https://huagongshe.com/reaction/1926406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3-chlorobenzonitrileHCID 519896—
Reactant2,5-Dichloro-1,3-benzothiazoleHCID 13314816—
Reactant2-Sulfanylidene-2,3-dihydro-1,3-benzothiazole-6-carbonitrileHCID 178509504—
Product2-Chloro-1,3-benzothiazole-6-carbonitrileHCID 21985859—

Reaction Conditions

Temperature120 °C

Reaction Steps

The title compound was prepared from 4-amino-3-chlorobenzonitrile via 2-mercapto-1,3-benzothiazole-6-carbonitrile as described for 2,5-dichloro-1,3-benzothiazole except that in the first step the reaction mixture was heated to 120° C. for 12 h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178668B2
Source datasetuspto-grants-2012_05
ORD IDord-5c50be31205b46e39585702495995ccb
Source noteuspto-grants-2012_05