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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746139Generated: November 3, 2026

Methyl 5-hydroxypyridine-2-carboxylate → 3-(Pyridin-3-yloxy)-4,5-dihydroisoxazole

https://huagongshe.com/reaction/1746139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-hydroxypyridine-2-carboxylateHCID 4715126—
Reactant3-Bromo-4,5-dihydroisoxazoleHCID 21983498—
Product3-(Pyridin-3-yloxy)-4,5-dihydroisoxazoleHCID 66818532—

Reaction Steps

3-(pyridin-3-yloxy)-4,5-dihydroisoxazole I-215a and I-215b were prepared in 2 steps compound from racemic compound I-21. Bromo-4,5-dihydroisoxazole I-21 was reacted with 5-hydroxy picolinic acid methyl ester using Method 5 followed by hydrolysis using the analogous conditions as in example 94. These compounds can be separated using chiral HPLC methods known in the art. For example, see chiral HPLC Method disclosed herein. [M+H]+=418.3 m/z. Activity: B

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149465B2
Source datasetuspto-grants-2015_10
ORD IDord-9c8fbccc2892440e9c5ee4a48bc2d3d2
Source noteuspto-grants-2015_10