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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975813Generated: October 25, 2026

Hydrochloric Acid → 1-(8-Aza-bicyclo[3.2.1]oct-8-yl)-4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-2-phenyl-butan-1-one

https://huagongshe.com/reaction/975813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant(1R,5S)-8-Azabicyclo[3.2.1]octaneHCID 637985—
ReactantTropaneHCID 637986—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-[4-(2-Methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acidHCID 9863428—
Reactant3-AcetyltropineHCID 10559369—
ReactantHydrate;dihydrochlorideHCID 21226127—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product1-(8-Aza-bicyclo[3.2.1]oct-8-yl)-4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-2-phenyl-butan-1-oneHCID 19968356—

Reaction Steps

A mixture of 4-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acid (4.0 g, 11.3 mmole), desmethyltropane (1.7 g, 15.3 mmole, prepared from tropane by the method used by R. A. Olofson et. al., J. Org. Chem., 1984, 49(11), 2081, for the conversion of O-acetyltropine to O-acetyldesmethyltropine), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (2.2 g, 11.3 mmole) and triethylamine (0.19.8 mmole) in methylene chloride (25 mL) was stirred at ambient temperature for 48 hr. The mixture was poured into 1 N sodium hydroxide (100 mL) and extracted with ethyl acetate (3×100 mL). The combined ethyl acetate layer was washed with water (100 mL) and brine (100 mL), dried over anhydrous magnesium sulfate, filtered and concentrated under vacuum to give crude product. Purification of this material by column chromatoghaphy (silica gel with 1% ammonia in ethyl acetate as eluant) followed by the treatment with 1.1 equivalent of 1N hydrogen chloride in ether gave 2.5 g of the title compound as the hydrochloride hemihydrate, m.p. 225°-228° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05610154
Source datasetuspto-grants-1997_03
ORD IDord-a2384bbb1ffa436092f760bf01f3f5a5
Source noteuspto-grants-1997_03