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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569963Generated: October 30, 2026

Dimethylformamide → HCID 12899546, compound

https://huagongshe.com/reaction/569963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-PhenylpiperazineHCID 7096—
ReactantHCID 21243013HCID 21243013—
SolventChloroformHCID 6212—
ProductHCID 12899546HCID 12899546—

Reaction Steps

5.1 Grams of 7-(3-chloro-2-hydroxypropoxy)-3,4-dihydrocarbostyril and 8 g of 4-phenylpiperazine are mixed with 50 ml of dimethylformamide and reacted at 50°-60° C. for 5 hours under stirring conditions. The reaction mixture is concentrated under a reduced pressure to dryness and the residue thus obtained is dissolved in 80 ml of chloroform, then the chloroform layer is washed 3 times with 5% of sodium hydrogencarbonate aqueous solution and washed 3 times with water and dried with anhydrous sodium sulfate. Chloroform is removed by distillation under a reduced pressure and the residue thus obtained is purified by a silica gel-chromatography [silica gel: Wako C-200, extracting solvent:chloroform:methanol=30:1 (v/v)]. Then the extracted product is converted into its hydrochloride by using ethanol containing hydrogen chloride and ethanol is removed by distillation under a reduced pressure. The thus obtained residue is recrystallized from water to obtain 5.6 g of 7-[2-hydroxy-3-(4-phenylpiperazinyl)propoxy]-3,4-dihydrocarbostyril.monohydrochloride.1/2 hydrate in the form of colorless crystals with a melting point of 122° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734416
Source datasetuspto-grants-1988_03
ORD IDord-feba0b4fad4c4f9394527d247c0f5daf
Source noteuspto-grants-1988_03