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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564884Generated: October 31, 2026

Triethylamine → HCID 86757778, compound

https://huagongshe.com/reaction/564884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-((4-Phenyl-4-piperidyl)carbonyl)pyrrolidine monohydrochlorideHCID 3019484—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 18319935HCID 18319935—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
SolventTitanium isopropoxideHCID 11026—
ProductHCID 86757778HCID 8675777855%

Reaction Steps

A solution of intermediate 15 (0.01 mol), 1-(4-phenyl-4-piperidinylcarbonyl)-pyrrolidine hydrochloride (0.01 mol) and triethylamine (0.015 mol) in THF (10 ml) and titanium(IV)isopropoxide (3.72 ml) was stirred at RT for 4 hours. Ethansol (10 ml) and sodium cyanoborohydride (0.01 mol) were added. The mixture was stirred for a few hours. Ice and ethanol (10 ml) were added and the mixture was stirred at RT for 30 minutes and then filtered over decalite. The solvent was evaporated and the residue extracted with CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by HPLC over silica gel (eluent: CH2Cl2/CH3OH 95/5). Two pure fractions were collected and their solvents were evaporated. The residue was crystallized from DIPE. The precipitate was filtered off and dried, yielding 4.07 g of (±)-cis-1-[3,5-bis(trifluoromethyl)-benzoyl]-4-[4-phenyl-4-(1-pyrrolidinylcarbonyl)-1-piperidinyl]-2-[[4-(trifluoromethyl)-phenyl]methyl]-piperdine (55% ) compound 111) and 1.3 g of (±)-trans-1-[3,5-bis(trifluoromethyl-benzoyl]-4-[4-phenyl-4-(1-pyrroldinylcarbonyl)-1-piperidinyl]-2-[[4-(trifluoromethyl)-phenyl]methyl]-piperidine (18%) (compound 112).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169097A
Source datasetuspto-grants-2001_01
ORD IDord-7300b36fbb724899ac45b65c1c2993f2
Source noteuspto-grants-2001_01