Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746127Generated: October 25, 2026

4-Butoxybenzaldehyde → 3-(Pyrimidin-5-yloxy)-4,5-dihydroisoxazole

https://huagongshe.com/reaction/1746127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ButoxybenzaldehydeHCID 79813—
ReactantPyrimidin-5-olHCID 565855—
Reactant3-Bromo-4,5-dihydroisoxazoleHCID 21983498—
Product3-(Pyrimidin-5-yloxy)-4,5-dihydroisoxazoleHCID 86650564—

Reaction Steps

3-(pyrimidin-5-yloxy)-4,5-dihydroisoxazole I-139a and I-139b was prepared in 3 steps from 4-butoxybenzaldehyde using Method 8 followed by cycloaddition using Method 1. The resulting bromo-4,5-dihydroisoxazole was reacted with 5-hydroxypyrimidine using Method 5. These compounds can be separated using chiral HPLC methods known in the art. For example, see chiral HPLC Method disclosed herein. [M+H]+=314.9 m/z. Activity: A

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149465B2
Source datasetuspto-grants-2015_10
ORD IDord-cf1212bc9584496e8775f6f1bf65c0c6
Source noteuspto-grants-2015_10