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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731635Generated: October 30, 2026

2-Amino-5-bromopyridine → HCID 24738993, compound

https://huagongshe.com/reaction/731635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyridineHCID 70622—
Reactant4-(Bromoacetyl)-5-methyl-3-phenylisoxazoleHCID 2735531—
ProductHCID 24738993HCID 2473899342%

Reaction Steps

As described for Example 1, 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (140 mg, 0.5 mmol) was converted, using 2-amino-5-bromopyridine instead of 2-aminopyridine, to the title compound (75 mg, 42%) which was obtained as a yellow gum. MS: m/e=354.1/356.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585874B2
Source datasetuspto-grants-2009_09
ORD IDord-9af54248dcb546f8abf11fd1a9a91a3a
Source noteuspto-grants-2009_09