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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334565Generated: October 29, 2026

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

https://huagongshe.com/reaction/334565

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant2-(But-3-ynyl)-5-phenyloxazoleHCID 86086917—
Product2-(4-(5-Phenyloxazol-2-yl)but-1-ynyl)pyridineHCID 116662569.4%

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 numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-6f0b28959a59438099ea885640a748f6
Source noteuspto-grants-2014_11