Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614635Generated: November 1, 2026

Hydrochloric Acid → 1-[4-[3-[4-[(4-Fluorophenyl)[(4-fluorophenyl)amino]methyl]-1-piperidinyl]propoxy]phenyl]-2-methyl-1-propanone dihydrochloride

https://huagongshe.com/reaction/1614635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantN,alpha-bis(4-fluorophenyl)-4-piperidinemethanamineHCID 19771957—
Reactant1-[4-(3-Chloropropoxy)phenyl]-2-methyl-1-propanoneHCID 19772013—
Solvent1-ButanolHCID 263—
SolventDichloromethaneHCID 6344—
Product1-[4-[3-[4-[(4-Fluorophenyl)[(4-fluorophenyl)amino]methyl]-1-piperidinyl]propoxy]phenyl]-2-methyl-1-propanone dihydrochlorideHCID 19772097—

Reaction Steps

A mixture of N,α-bis(4-fluorophenyl)-4-piperidinemethanamine (4.63 g, 0.0153 mol), 1-[4-(3-chloropropoxy)phenyl]-2-methyl-1-propanone (3.69 g, 0.0153 mol), and potassium carbonate (2.76 g, 0.02 mol) was heated at reflux 16 h in 350 mL 1-butanol containing sodium iodide (0.2 g). The reaction was concentrated to dryness and partitioned between chloroform and water. The chloroform layer was then extracted with 5% sodium hydroxide and dried (Na2SO4). The chloroform was removed to give a red oil. This material was subjected to flash chromatography on silica gel using 2% methanol in methylene chloride to accomplish elution. Fractions of similar purities were combined, and solvents removed to give an oil. The oil was converted to the HCl salt and recrystallized from methanol-diethyl ether to give a white solid. This solid was dried 16 h at 78° C. in vacuo. The procedure utilized here furnished 5.26 g (59%) of white crystalline product, mp 221° -223° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198449
Source datasetuspto-grants-1993_03
ORD IDord-7f2b906195254c3ca0add4bbea859e38
Source noteuspto-grants-1993_03