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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871006Generated: October 30, 2026

Potassium Carbonate → Methyl 4-[({[4-cyano-3-(4-nitrophenyl)isothiazol-5-yl]amino}carbonyl)amino]butanoate

https://huagongshe.com/reaction/871006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-isocyanatobutanoateHCID 2759393—
Reactant5-Amino-3-(4-nitrophenyl)isothiazole-4-carbonitrileHCID 69055185—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-[({[4-cyano-3-(4-nitrophenyl)isothiazol-5-yl]amino}carbonyl)amino]butanoateHCID 8668922780.1%

Reaction Steps

A solution of 5-amino-3-(4-nitrophenyl)isothiazole-4-carbonitrile (25.0 g, 0.101 mol) in tetrahydrofuran (300 mL) dimethylsulfoxide (40 mL) at ambient temperature was treated with potassium carbonate (35.0 g, 0.25 mol). The resulting mixture was stirred at ambient temperature for 15 min. The reaction mixture was treated with 4-isocyanato-butyric acid methyl ester (21.8 g, 0.15 mol) at ambient temperature. The mixture was stirred at ambient temperature overnight. The reaction mixture was filtered through celite and filtrate concentrated in vacuo. The residue was dissolved EtOAc (600 mL) and washed with water and brine then dried (sodium sulfate), filtered, solvent concentrated in vacuo. The crude residue was purified by column chromatography (20% ethyl acetate in dichloromethane) to give the title compound as a light brown solid (31.5 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969583B2
Source datasetuspto-grants-2015_03
ORD IDord-0007843c66bf419a9d98952a8baaede5
Source noteuspto-grants-2015_03