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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903200Generated: November 1, 2026

Isopropanol → HCID 13107975, compound

https://huagongshe.com/reaction/1903200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant6-Hydroxy-3,4-dihydro-2(1H)-quinolinoneHCID 2774040—
ReactantHCID 53721842HCID 53721842—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 13107975HCID 13107975—

Reaction Steps

Into 100 ml of isopropanol were added 1.6 g of 6-hydroxy-3,4-dihydrocarbostyril and 1.8 ml of DBU. The mixture was refluxed under stirring and 4.2 g of 4-cyclohexyl-1-γ-bromobutylpiperazine was added thereto. After the addition operation, the reaction mixture was further refluxed under stirring for 8 hours, then concentrated. The residue thus obtained was extracted with chloroform and the chloroform layer was washed with 1N-NaOH aqueous solution and water, then dried with anhydrous sodium sulfate. The drying agent was removed by filtration and the mother liquor was concentrated. The residue thus obtained was treated by a silica-gel column chromatography [the solvent used was a mixture of chloroform:methanol=20:1 (vol/vol)]. 2.8 Grams of 6-[3-(4-cyclohexyl-1-piperazinylcarbonyl)propoxy]-3,4-dihydrocarbostyril was obtained as in the form of colorless needle-like substance. Melting point: 133°-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435404
Source datasetuspto-grants-1984_03
ORD IDord-65aa5d25604944c5af55e93dd097a158
Source noteuspto-grants-1984_03