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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334574Generated: October 29, 2026

2-Bromopyridine → HCID 11687442, compound

https://huagongshe.com/reaction/334574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantHCID 86086739HCID 86086739—
ProductHCID 11687442HCID 1168744239%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 1, from 2-bromopyridine (92 mg, 0.58 mmol) and 2-(but-3-ynyl)oxazolo[5,4-b]pyridine (100 mg, 0.58 mmol). The crude residue was purified by flash chromatography (DCM/MeOH 98.5:1.5 to 98:2) to yield 56 mg (0.22 mmol, 39%) of 2-(4-(pyridin-2-yl)but-3-ynyl)oxazolo[5,4-b]pyridine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-78d5f892235e425493c5403550513285
Source noteuspto-grants-2014_11