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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154956Generated: October 27, 2026

Sodium Chloride → 1-methyl-6-[3-(N-cyclohexyl-N-methylaminocarbonyl)propoxy]-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1154956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium IodideHCID 5238—
ReactantSodiumHCID 5360545—
Reactant4-Chloro-N-cyclohexyl-N-methylbutanamideHCID 13208297—
Reactant6-Hydroxy-1-methyl-3,4-dihydroquinolin-2(1H)-oneHCID 21931828—
SolventMethanolHCID 887—
Product1-methyl-6-[3-(N-cyclohexyl-N-methylaminocarbonyl)propoxy]-3,4-dihydrocarbostyrilHCID 1557292642.2%

Reaction Steps

0.5 Gram of metallic sodium is dissolved in 50 ml of methanol under ice cooling, followed by addition thereto of 3.4 g of 1-methyl-6-hydroxy-3,4-dihydrocarbostyril, 3.2 g of sodium iodide and 5.0 g of N-methyl-N-(4-chlorobutyryl)cyclohexylamine and 4.5-hour reflux under agitation. After the reaction, the reaction solution is poured into 400 ml of saturated NaCl solution and the precipitated crystals are filtered out and washed with water. The resultant crude crystals are recrystallized from ligroin to produce 2.9 g of 1-methyl-6-[3-(N-cyclohexyl-N-methylaminocarbonyl)propoxy]-3,4-dihydrocarbostyril in the form of colorless needle-like crystals with melting point of 104.5°-106.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298739
Source datasetuspto-grants-1981_11
ORD IDord-7f2b5c96b8c240d9b93c9cf9ca12f5a8
Source noteuspto-grants-1981_11