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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398902Generated: October 30, 2026

4-Amino-3,5-dimethylisoxazole → HCID 68764632, compound

https://huagongshe.com/reaction/1398902

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3,5-dimethylisoxazoleHCID 182040—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantEthyl 4-[2,4-dichloro-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]butanoateHCID 68761768—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 68764632HCID 6876463250%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of ethyl 4-[2,4-dichloro-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]butanoate (Reference Example 33; 740 mg, 2.0 mmol), 3,5-dimethylisoxazol-4-amine (672 mg, 6.0 mmol) and p-toluenesulfonic acid monohydrate (380 mg, 2.0 mmol) in 1-methyl-2-pyrrolidinone (3 mL) was stirred at 130° C. for 16 hr. After cooling, the mixture was diluted with ethyl acetate, washed with aqueous sodium bicarbonate and brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel eluting with a 20-60% ethyl acetate/n-hexane gradient mixture followed by recrystallization from ethyl acetate/n-hexane to give the title compound (450 mg, 1.0 mmol, 50%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-1f2e34eebedd4f4e9849f4ce1c1de780
Source noteuspto-grants-2014_12