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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731615Generated: October 30, 2026

2-Amino-4-methylpyridine → HCID 24738342, compound

https://huagongshe.com/reaction/731615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methylpyridineHCID 1533—
Reactant4-(Bromoacetyl)-5-methyl-3-phenylisoxazoleHCID 2735531—
ProductHCID 24738342HCID 2473834219%

Reaction Steps

As described for Example 2, 4-(bromoacetyl)-5-methyl-3-phenylisoxazole (commercially available) (140 mg, 0.5 mmol) was converted, using 2-amino-4-methylpyridine instead of 2-amino-3-methylpyridine, to the title compound (22 mg, 19%) which was obtained as a yellow solid. MS: m/e=290.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585874B2
Source datasetuspto-grants-2009_09
ORD IDord-18664e352fd043a0a50225fdbdd51835
Source noteuspto-grants-2009_09