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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358508Generated: November 1, 2026

Hydrochloric Acid → HCID 13369835, compound

https://huagongshe.com/reaction/358508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13369832HCID 13369832—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 13369835HCID 13369835—

Reaction Steps

0.5 Gram of 6-[4-(2-hydroxypropyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril and 0.3 ml of triethylamine were dissolved in 10 ml of dichloromethane, the mixture was stirred at a room temperature, 0.15 g of acetyl chloride was added slowly thereto and further stirred at a room temperature for 1 hour. The reaction mixture was poured into a saturated sodium bicarbonate aqueous solution and extracted with chloroform. The organic layer was washed with water and a saturated sodium chloride aqueous solution and extracted with chloroform. The organic layer was washed with water and a saturated sodium chloride aqueous solution then dried with anhydrous sodium sulfate. The solvent was removed by distillation under a reduced pressure and the residue obtained was treated by means of a silica gel column chromatography, then the objective product was dissolved in methanol and converted into the hydrochloride by adding a concentrated hydrochloric acid. Recrystallized from water-acetone to obtain 0.22 g of 6-[4-(2-acetoxypropyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril monohydrochloride. Melting point: 239°-241° C. (decomposed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04468402
Source datasetuspto-grants-1984_08
ORD IDord-2cbbcea2b87a41c0a4062f421b681d19
Source noteuspto-grants-1984_08