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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731634Generated: October 30, 2026

2-Amino-5-chloropyridine → HCID 24738991, compound

https://huagongshe.com/reaction/731634

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chloropyridineHCID 66174—
Reactant4-(Bromoacetyl)-5-methyl-3-phenylisoxazoleHCID 2735531—
ProductHCID 24738991HCID 2473899153%

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-chloropyridine instead of 2-aminopyridine, to the title compound (82 mg, 53%) which was obtained as a yellow gum. MS: m/e=310.3[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585874B2
Source datasetuspto-grants-2009_09
ORD IDord-b183fcedb85f44629f372d02523b21ec
Source noteuspto-grants-2009_09