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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636557Generated: November 1, 2026

2-(4-Aminophenyl)-6-methylbenzothiazole → 2-Bromo-4-(6-methyl-2-benzothiazolyl)benzenamine

https://huagongshe.com/reaction/1636557

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Aminophenyl)-6-methylbenzothiazoleHCID 7087—
ReactantBromineHCID 24408—
SolventDichloromethaneHCID 6344—
Product2-Bromo-4-(6-methyl-2-benzothiazolyl)benzenamineHCID 38794985.3%

Reaction Steps

2-(4'-Aminophenyl)-6-methylbenzothiazole (0.6 g, 2.5 mmol) was treated with bromine (0.403 g, 2.5 mmol) in dichloromethane according to the above-described general procedure for bromination. Crude product was purified by flash chromatography on silica gel, using ethyl acetate-hexane (1:3) as eluent, to give brown small crystals (0.68 g, 85.3%), m.p. 187.9-189.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034246
Source datasetuspto-grants-2000_03
ORD IDord-3ebd9a092d444e0db1f15463225f7f7f
Source noteuspto-grants-2000_03