Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731633Generated: October 30, 2026

4-(Bromoacetyl)-5-methyl-3-phenylisoxazole → HCID 24738992, compound

https://huagongshe.com/reaction/731633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromoacetyl)-5-methyl-3-phenylisoxazoleHCID 2735531—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
ProductHCID 24738992HCID 2473899213%

Reaction Steps

As described for Example 2, 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (112 mg, 0.4 mmol) was converted, using 2-amino-5-fluoropyridine instead of 2-amino-3-methylpyridine, to the title compound (15 mg, 13%) which was obtained as a yellow solid. MS: m/e=294.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585874B2
Source datasetuspto-grants-2009_09
ORD IDord-5ae639013ced40b7819a119cbae6af95
Source noteuspto-grants-2009_09