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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334600Generated: October 31, 2026

4-Chloropyrimidine → 2-(4-(Pyrimidin-4-yl)but-3-ynyl)benzo[d]oxazole

https://huagongshe.com/reaction/334600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloropyrimidineHCID 642834—
Reactant2-(But-3-ynyl)benzo[d]oxazoleHCID 86086907—
Product2-(4-(Pyrimidin-4-yl)but-3-ynyl)benzo[d]oxazoleHCID 6659812217.3%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 1, from 4-chloropyrimidine (85 mg, 0.74 mmol) and 2-(but-3-ynyl)benzo[d]oxazole (127 mg, 0.74 mmol). The crude residue was purified by flash chromatography (cyclohexane/AcOEt 3:2) to yield 32 mg (128 μmol, 17%) of 2-(4-(pyrimidin-4-yl)but-3-ynyl)benzo[d]oxazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-1079d02265d9423b9fd489504d6fecc8
Source noteuspto-grants-2014_11