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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372678Generated: November 1, 2026

2-Bromo-4-chlorobenzothiazole → HCID 58778599, compound

https://huagongshe.com/reaction/1372678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-chlorobenzothiazoleHCID 77178—
ReactantMethyl 2-(4-amino-3-chlorophenyl)acetateHCID 13616273—
ReactantPyridinium.p-toluenesulfonateHCID 22033616—
SolventO-XyleneHCID 7237—
ProductHCID 58778599HCID 5877859958.2%

Reaction Steps

In xylene (7 ml), 2-bromo-4-chlorobenzothiazole (647 mg, 2.60 mmol), methyl 4-amino-3-chlorophenylacetate (520 mg, 2.60 mmol), and pyridinium•p-toluenesulfonate (PPTS) (200 mg, 0.80 mmol) were heated under reflux for 7 hours. After cooling, the reaction mixture was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane/ethyl acetate (6:1, v/v) eluate fractions, methyl (4-(4-chloro-2-benzothiazolyl)amino-3-chlorophenyl)acetate (556 mg, 58%) was obtained as a yellow amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-8b7e2bf5b4fc446d9ef604a3fd736b30
Source noteuspto-grants-2007_01