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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731641Generated: October 30, 2026

2-Amino-4-bromopyridine → HCID 24738828, compound

https://huagongshe.com/reaction/731641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-bromopyridineHCID 693282—
Reactant4-(Bromoacetyl)-5-methyl-3-phenylisoxazoleHCID 2735531—
ProductHCID 24738828HCID 2473882833%

Reaction Steps

As described for Example 2, 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (2.0 g, 7.2 mmol) was converted, using 2-amino-4-bromopyridine instead of 2-amino-3-methylpyridine, to the title compound (824 mg, 33%) which was obtained as a light yellow foam. MS: m/e=354.1/355.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585874B2
Source datasetuspto-grants-2009_09
ORD IDord-b6c0ffc1a63b4c718ae3196f7fc7fa65
Source noteuspto-grants-2009_09