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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422293Generated: October 29, 2026

2-Bromopyridine → 2-(4-(5-Phenyloxazol-2-yl)but-1-ynyl)pyridine

https://huagongshe.com/reaction/422293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant2-(But-3-ynyl)-5-phenyloxazoleHCID 86086917—
Product2-(4-(5-Phenyloxazol-2-yl)but-1-ynyl)pyridineHCID 1166625618.8%
Product4-(5-Phenyloxazol-2-yl but-1-ynyl)pyridineHCID 86630242—

Reaction Steps

The title compound was prepared in accordance with the general method of Example 1, from 2-bromopyridine (25 mg, 0.16 mmol) and 2-(but-3-ynyl)-5-phenyloxazole (31 mg, 0.16 mmol). The crude residue was purified by flash chromatography (DCM/MeOH 99:1) and SCX column (DCM/MeOH 95:5, DCM/MeOH/NH4OH 90:5:0.1 to 90:9:1) to yield 4.0 mg (15 μmol, 9%) of 2-(4-(5-phenyloxazol-2-yl)but-1-ynyl)pyridine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-acd8210762094eaf9c66bd8ff627327e
Source noteuspto-grants-2012_01