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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27781Generated: October 25, 2026

2-Hydroxyquinoline → 8-Cyclohexylcarbonyloxy-5-(1-hydroxy-2-isopropylaminobutyl)-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/27781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-HydroxyquinolineHCID 6038—
ReactantSodium MethoxideHCID 10942334—
Reactant5-(1-Hydroxy-2-isopropylaminobutyl)-8-hydroxy-3,4-dihydrocarbostyril hydrochlorideHCID 23342111—
SolventMethanolHCID 887—
Product8-Cyclohexylcarbonyloxy-5-(1-hydroxy-2-isopropylaminobutyl)-3,4-dihydrocarbostyrilHCID 23342118—

Reaction Conditions

Temperature10 °C

Reaction Steps

3.28 g of 5-(1-hydroxy-2-isopropylaminobutyl)-8-hydroxy-3,4-dihydrocarbostyril hydrochloride was dissolved in 50 ml of methanol, and a 10% methanolic solution of sodium methylate was added to the solution in an amount of 2 moles per mole of the starting carbostyril compound. The resulting mixture was concentrated to dryness, and the residue was dissolved in dimethylformamide. 1.6 g of cyclohexanecarboxylic acid chloride was added to the solution and the mixture was stirred for 2 hours at a temperature of 10° C. The reaction mixture was poured into ice-water and the mixture was extracted with chloroform. A mixture of diethyl ether and petroleum benzene was added to the extract to obtain 1.2 g of crystalline 8-cyclohexylcarbonyloxy-5-(1-hydroxy-2-isopropylaminobutyl)-3,4-dihydrocarbostyril having a melting point of 148°-149° C. (after recrystallization from chloroform-n-hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04223137
Source datasetuspto-grants-1980_09
ORD IDord-8764f7097d814378b0920f93d835f036
Source noteuspto-grants-1980_09