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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060195Generated: November 1, 2026

Sodium Bicarbonate → HCID 86756486, compound

https://huagongshe.com/reaction/1060195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(+/-)-1-[3,5-Bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-(1-piperazinyl)piperidineHCID 18630855—
ReactantHCID 18630858HCID 18630858—
SolventEthanolHCID 702—
ProductHCID 86756486HCID 8675648659.8%

Reaction Steps

A mixture of compound 15 (0.005 mol), N-[2-(3,4-dichlorophenyl)-4-[(methylsulfonyl)oxy]butyl]-N-methyl benzamide (0.0055 mol) and NaHCO3 (0.0055 mol) in ethanol (50 ml) was stirred and refluxed for 6 hours. The solvent was evaporated, the residue was taken up in water and extracted with CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified over silica gel on a glass filter (eluent: CH2Cl2/CH3OH 100/0, 99/1, 98/2 and 97/3). The pure fractions were collected and the solvent was evaporated. The residue was converted into the fumaric acid salt (1:2) with ethanol. The precipitate was filtered off and dried, yielding 1.42 g (27%) of (±)-cis-N-[4-[4-[1-[3,5-bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-piperidinyl]-1-piperazinyl]-2-(3,4-dichlorophenyl)butyl]-N-methylbenzamide (E)-2-butenedioate(1:2) (compound 93).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521621B1
Source datasetuspto-grants-2003_02
ORD IDord-47a54a90c64948ff88d19aeb5bd8dae2
Source noteuspto-grants-2003_02