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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903199Generated: October 31, 2026

Isopropanol → HCID 20468115, compound

https://huagongshe.com/reaction/1903199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 20468176HCID 20468176—
ReactantHCID 53721842HCID 53721842—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 20468115HCID 20468115—

Reaction Steps

Into 100 ml isopropanol were added 2.0 g of 1-allyl-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)]. 3.5 Grams of 1-allyl-6-[3-(4-cyclohexyl-1-piperazinylcarbonyl)propoxy]-3,4-dihydrocarbostyril was obtained as in the form of a colorless syrupy substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435404
Source datasetuspto-grants-1984_03
ORD IDord-12518a2a80874aac9e1ebc2ce2cfda99
Source noteuspto-grants-1984_03