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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422261Generated: October 28, 2026

2-Bromopyridine → 2-(4-(Pyridin-2-yl)but-3-ynyl)benzo[d]oxazole

https://huagongshe.com/reaction/422261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant2-(But-3-ynyl)benzo[d]oxazoleHCID 86086907—
ReactantHCID 178526334HCID 178526334—
SolventDichloromethaneHCID 6344—
Product2-(4-(Pyridin-2-yl)but-3-ynyl)benzo[d]oxazoleHCID 1163738379.7%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 1, from 2-bromopyridine (746 mg, 4.67 mmol) and 2-(but-3-ynyl)benzo[d]oxazole (800 mg, 4.67 mmol). Reaction time: 3 hours. The crude residue was dissolved in DCM, syn-2-pyridinecarboxaldoxime (684 mg, 5.60 mmol) was added and the reaction mixture was stirred overnight. The solvent was evaporated and the resulting crude product was purified by flash chromatography (DCM/MeOH 99:1) to yield 923 mg (3.72 mmol, 79%) of 2-(4-(pyridin-2-yl)but-3-ynyl)benzo[d]oxazole as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-56b99cf6d48e475f9638b0a8ea1876e6
Source noteuspto-grants-2012_01