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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422298Generated: October 30, 2026

Benzoxazole → 2-(4-(5-Fluoropyridin-2-yl)but-3-ynyl)benzo[d]oxazole

https://huagongshe.com/reaction/422298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoxazoleHCID 9228—
Reactant2-Bromo-5-fluoropyridineHCID 2783171—
Product2-(4-(5-Fluoropyridin-2-yl)but-3-ynyl)benzo[d]oxazoleHCID 116876029.8%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 1, from 2-bromo-5-fluoropyridine (200 mg, 1.14 mmol) and 2-but-3-ynyl)benzo[d]oxazole (195 mg, 1.14 mmol, Example 8(A)). The crude residue was purified by flash chromatography (DCM/MeOH 99:1) and SCX column (DCM/MeOH 100:0 to 94:6, DCM/MeOH 94:5:1 to 90:8:2) to yield 15 mg (56 μmol, 5%) of 2-(4-(5-fluoropyridin-2-yl)but-3-ynyl)benzo[d]oxazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-18a3d354a1e3478c873f1f400931cbed
Source noteuspto-grants-2012_01