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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732723Generated: October 30, 2026

Ethyl Acetate → HCID 68912483, compound

https://huagongshe.com/reaction/732723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantEthyl chloroformateHCID 10928—
Reactant1-Acetylpiperidine-4-carboxylic acidHCID 117255—
ReactantHCID 86628564HCID 86628564—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 68912483HCID 68912483—

Reaction Steps

An 8.0 ml ethyl acetate solution of 318 mg of 1-acetylpiperidine-4-carboxylic acid was mixed with 0.18 ml of ethyl chloroformate, 0.52 ml of triethylamine and 400 mg of tert-butyl [(1R)-1-(1-naphthyl)ethyl][(4-phenylpyrrolidin-3-yl)methyl]carbamate in that order and stirred at room temperature for 30 minutes. This was mixed with 10 ml of water and extracted with ethyl acetate. The solvent was evaporated, and the thus obtained residue was purified by a silica gel column chromatography (chloroform-methanol). This was treated with 4 M hydrogen chloride/ethyl acetate and concentrated to dryness to obtain 75 mg of (1R)—N-({1-[(1-acetylpiperidin-4-yl)carbonyl]-4-phenylpyrrolidin-3-yl}methyl)-1-(1-naphthyl)ethanamine hydrochloride as a pale pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585886B2
Source datasetuspto-grants-2009_09
ORD IDord-b9301001efa640a08e761fdc40a889f3
Source noteuspto-grants-2009_09