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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334579Generated: October 29, 2026

4-Iodo-2-methyl-1,3-thiazole → 7-Chloro-5-fluoro-2-(4-(2-methylthiazol-4-yl)but-3-ynyl)benzo[d]oxazole

https://huagongshe.com/reaction/334579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-2-methyl-1,3-thiazoleHCID 53706790—
Reactant2-(But-3-ynyl)-7-chloro-5-fluorobenzo[d]oxazoleHCID 86086744—
Product7-Chloro-5-fluoro-2-(4-(2-methylthiazol-4-yl)but-3-ynyl)benzo[d]oxazoleHCID 1161674655.1%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 1, from 4-iodo-2-methylthiazole (200 mg, 0.89 mmol) and 2-(but-3-ynyl)-7-chloro-5-fluorobenzo[d]oxazole (199 mg, 0.89 mmol). The crude residue was purified by flash chromatography (cyclohexane/AcOEt 85:15) to yield 157 mg (0.49 mmol, 55%) of 7-chloro-5-fluoro-2-(4-(2-methylthiazol-4-yl)but-3-ynyl)benzo[d]oxazole as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-e9cfd103645748798fde2961421b9d18
Source noteuspto-grants-2014_11