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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577938Generated: November 2, 2026

Hydrochloric Acid → HCID 20570440, compound

https://huagongshe.com/reaction/1577938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantHCID 12751813HCID 12751813—
SolventAcetoneHCID 180—
ProductHCID 20570440HCID 2057044045.5%

Reaction Steps

0.66 g of 8-hydroxy-5-(2-hydroxy-3-isopropylaminopropoxy)-3,4-dihydrocarbostyril was suspended in 10 ml of acetone, and 3.0 ml of 1 N sodium hydroxide was added thereto to form a homogeneous solution. 0.35 g of cyclohexylcarbonyl chloride dissolved in a small amount of acetone was added dropwise to the solution while ice-cooling and stirring. After the reaction mixture was allowed to stand under ice-cooling for 30 minutes, 1 N hydrochloric acid was added thereto to adjust to a pH of 3. The solvent was evaporated under reduced pressure, and the residue was dissolved in water and extracted with chloroform. The aqueous layer was concentrated to dryness under reduced pressure, and the residue was purified by silica gel chromatography using chloroform-methanol (8:1 by volume) as an eluent. The solvent was evaporated, and the residue was recrystallized from methanol-diethyl ether to obtain 0.45 g of 8-cyclohexylcarbonyloxy-5-(2-hydroxy-3-isopropylaminopropoxy)-3,4-dihydrocarbostyril hydrochloride as colorless flake-like crystals having a melting point of 227°-228° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04289883
Source datasetuspto-grants-1981_09
ORD IDord-477756705f6647a5a7aa8e2caf28458a
Source noteuspto-grants-1981_09