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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154948Generated: October 31, 2026

N-Methylcyclohexylamine → Cilostamide

https://huagongshe.com/reaction/1154948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylcyclohexylamineHCID 7514—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant4-((2-Oxo-1,2-dihydroquinolin-6-yl)oxy)butanoic acidHCID 12866342—
SolventChloroformHCID 6212—
ProductCilostamideHCID 2753—

Reaction Steps

2.5 Grams of 6-(3-carboxypropoxy)carbostyril is suspended in 200 ml of chloroform, followed by addition of 1.5 ml of triethylamine, and then 1.2 g of thionyl chloride is added dropwise to the solution under agitation while maintaining the internal temperature at 0° to 20° C. After this addition, the mixture is agitated at the same temperature for 1 hour and then added dropwise with 2 ml of N-methylcyclohexylamine, followed by additional 3-hour agitation at room temperature. The reaction solution is washed well with a 5% aqueous K2CO3 solution, then further washed with water and diluted hydrochloric acid and then dried with anhydrous Na2SO4. After removing the solvent by distillation, the residue is refined by silica gel column chromatography (silica gel: Wakogel C-200; eluent: 10:1 chloroform/methanol (V/V)) and then recrystallized from chloroform-ethanol to obtain 0.4 g of 6-[3-(N-methyl-N-cyclohexylaminocarbonyl)propoxy]-carbostyril with melting point of 184.5°-186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298739
Source datasetuspto-grants-1981_11
ORD IDord-831eec8287e3463cbf94787c27680d39
Source noteuspto-grants-1981_11