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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910222Generated: October 29, 2026

2-Amino-5-bromopyrimidine → 5-[4-(6-Bromoimidazo[1,2-a]pyrimidin-2-yl)phenyl]-1,3-oxazole

https://huagongshe.com/reaction/910222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyrimidineHCID 231310—
Reactant2-Bromo-1-[4-(1,3-oxazol-5-yl)phenyl]-1-ethanoneHCID 86631886—
Solvent1,4-DioxaneHCID 31275—
Product5-[4-(6-Bromoimidazo[1,2-a]pyrimidin-2-yl)phenyl]-1,3-oxazoleHCID 6740550086.1%

Reaction Steps

2-Amino-5-bromopyrimidine (348 mg) and 2-bromo-1-[4-(1,3-oxazol-5-yl)phenyl]-1-ethanone (532 mg) were suspended in 1,4-dioxane (20 mL), followed by refluxing under heating overnight. Immediately after refluxing, the reaction mixture was filtered without being cooled, followed by washing with heated 1,4-dioxane and drying, to thereby yield the title compound (587 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022075B2
Source datasetuspto-grants-2011_09
ORD IDord-7d9150ae60a447fe97a2c80da206e44c
Source noteuspto-grants-2011_09