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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926414Generated: October 26, 2026

6-Chloro-m-anisidine → 2-Iodo-5-methoxy-1,3-benzothiazole

https://huagongshe.com/reaction/1926414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-m-anisidineHCID 75460—
Reactant2,3-DifluoroanilineHCID 78278—
Reactant7-Fluoro-2-iodobenzo[d]thiazoleHCID 67521180—
Product2-Iodo-5-methoxy-1,3-benzothiazoleHCID 18966972—

Reaction Steps

The title compound was prepared following the route for 7-fluoro-2-iodo-1,3-benzothiazole from 2,3-difluoroaniline, starting from 2-chloro-5-methoxyaniline and conducting the first step at 150° C. for 16 h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178668B2
Source datasetuspto-grants-2012_05
ORD IDord-9ac711b8b2eb44a5aff8e660f566aa97
Source noteuspto-grants-2012_05