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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264348Generated: October 30, 2026

Hydrochloric Acid → HCID 23112232, compound

https://huagongshe.com/reaction/2264348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
Reactant3-AminophenolHCID 11568—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23112221HCID 23112221—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 23112232HCID 23112232—

Reaction Steps

A mixture of 227 mg of 3-aminophenol, 3-(piperidin-1-ylmethyl)biphenyl-4-carboxylic acid (2.08 mmol), and sodium chloride was suspended into 7 ml of DMF and then 599 mg of 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide was added thereto at room temperature, followed by 10 hours of stirring. Ethyl acetate and a 1M aqueous hydrochloric acid solution were added to the reaction solution and sodium hydrogen carbonate was added to the aqueous layer obtained by an operation of separation until the aqueous layer was rendered basic. Ethyl acetate was added to the aqueous layer and an operation of separation was conducted. The resulting organic layer was dried over anhydrous magnesium sulfate and then the solvent was removed by evaporation. The obtained white solid was dissolved in ethanol and a 4M ethyl acetate solution of hydrochloric acid was added thereto, followed by removal of the solvent by evaporation. Ethanol and water were added to the obtained reside and crystallization was effected to obtain 436 mg of N-(3-hydroxyphenyl)-3-(piperidin-1-ylmethyl)biphenyl-4-carboxamide hydrochloride as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855198B2
Source datasetuspto-grants-2010_12
ORD IDord-b67d34a3251844eda5034004810f8366
Source noteuspto-grants-2010_12