Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911758Generated: November 2, 2026

3-Amino-5-methylisoxazole → HCID 57486825, compound

https://huagongshe.com/reaction/1911758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-5-methylisoxazoleHCID 66172—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-((Cyclobutylmethyl)(ethyl)amino)quinoline-3-carbaldehydeHCID 57444444—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 57486825HCID 5748682543%

Reaction Steps

5-Methyl-isoxazol-3-ylamine (0.098 g, 1 mmol) was added to a solution of 2-(cyclobutylmethyl-ethyl-amino)-quinoline-3-carbaldehyde (0.268 g, 1 mmol) in anhydrous methanol (5 mL) and acetic acid (0.15 mL) under nitrogen. After being stirred for 15 minutes at ambient temperature, sodium cyanoborohydride (0.19 g, 3 mmol) was added slowly, and the reaction mixture was stirred overnight. Afterwards, the solvent was evaporated in vacuo, and water (30 mL) and ethyl acetate (30 mL) were added to the residue. The organic layer was separated, washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by chromatography on silica gel, eluting with 1-5% methanol in dichloromethane, to afford the title compound (0.150 g, yield: 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604055B2
Source datasetuspto-grants-2013_12
ORD IDord-0386ca1f13a74f3eb11394d6fa838af8
Source noteuspto-grants-2013_12