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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154937Generated: October 27, 2026

Sodium Chloride → Cilostamide

https://huagongshe.com/reaction/1154937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantN-MethylcyclohexylamineHCID 7514—
Reactant4-((2-Oxo-1,2-dihydroquinolin-6-yl)oxy)butanoic acidHCID 12866342—
ReactantMethyl bromoformateHCID 15389422—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductCilostamideHCID 2753—

Reaction Steps

2.5 Grams of 6-(3-carboxy)propoxycarbostyril and 1.8 ml of pyridine are added to 50 ml of tetrahydrofuran, and then 1.0 ml of methyl bromoformate is added dropwise to said solution under external ice cooling and agitation while maintaining the internal temperature at 5°-15° C. after addition, the mixture is further agitated at room temperature for 1 hour and then added with 1.2 g of N-methylcyclohexylamine, followed by additional 3-hour agitation. The reaction solution is poured into 200 ml of saturated NaCl solution and the precipitated crystals are filtered out and washed with water. The obtained crude crystals are recrystallized from chloroform-ethanol to obtain 2.3 g of 6-[3-(N-methyl-N-cyclohexylaminocarbonyl)propoxy]carbostyril in the form of colorless needle-like crystals with m.p. of 184.5°-186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298739
Source datasetuspto-grants-1981_11
ORD IDord-5810647647504145b573b3275219579e
Source noteuspto-grants-1981_11