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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422273Generated: October 25, 2026

4-Bromo-2-methyl-1,3-thiazole → 2-(4-(2-Methylthiazol-4-yl)but-3-ynyl)benzo[d]oxazole

https://huagongshe.com/reaction/422273

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-methyl-1,3-thiazoleHCID 2763186—
Reactant2-(But-3-ynyl)benzo[d]oxazoleHCID 86086907—
Product2-(4-(2-Methylthiazol-4-yl)but-3-ynyl)benzo[d]oxazoleHCID 115145452%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 1, from 4-bromo-2-methylthiazole (47 mg, 2.7 mmol) and 2-(but-3-ynyl)benzo[d]oxazole (454 mg, 2.65 mmol, Example 8(A)). The reaction mixture was stirred for one day under reflux. The crude residue was purified by flash chromatography (cyclohexane/AcOEt 4:1) and trituration with pentane to yield 14-mg (52 μmol, 2%) of 2-(4-(2-methylthiazol-4-yl)but-3-ynyl)benzo[d]oxazole as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-8f0101e5b1b0482b96d339242f507098
Source noteuspto-grants-2012_01