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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731632Generated: October 30, 2026

2-Amino-5-methylpyridine → HCID 24739640, compound

https://huagongshe.com/reaction/731632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methylpyridineHCID 15348—
Reactant4-(Bromoacetyl)-5-methyl-3-phenylisoxazoleHCID 2735531—
ProductHCID 24739640HCID 2473964021%

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-methylpyridine instead of 2-amino-3-methylpyridine, to the title compound (24 mg, 21%) which was obtained as a yellow oil. MS: m/e=290.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585874B2
Source datasetuspto-grants-2009_09
ORD IDord-4de6201459c34d7eb37564b3ed0a871a
Source noteuspto-grants-2009_09