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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858366Generated: October 28, 2026

Triethylamine → 2-Ethoxy-4-(3-((S)-3-methy-1-(2-piperidin-1-yl-phenyl)-butylamino)-2-oxo-propyl)-benzoic acid ethyl ester

https://huagongshe.com/reaction/858366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
Reactant3-Ethoxy-4-ethoxycarbonylphenylacetic acidHCID 10131212—
Reactant3-Methyl-1-(2-piperidinophenyl)-1-butylamine, (S)-HCID 10514609—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product2-Ethoxy-4-(3-((S)-3-methy-1-(2-piperidin-1-yl-phenyl)-butylamino)-2-oxo-propyl)-benzoic acid ethyl esterHCID 1064841973%

Reaction Conditions

Temperature30 °C

Reaction Steps

Pivaloyl chloride (5.4 g, 45 mmol) was added to a mixture of 3-ethoxy-4-ethoxycarbonyl phenylacetic acid (10.0 g, 40 mmol), toluene (50 ml) and triethylamine (5.0 g, 49 mmol) at −5° C. and stirred for 1 hour. A solution of (S)-3-methyl-1-(2-piperidinophenyl)-1-butylamine (9.8 g, 40 mmol) in toluene (20 ml) was then added at below 10° C. The temperature of the reaction mixture was raised to 30° C. and the mixture stirred overnight. It was then washed with water and saturated sodium bicarbonate solution. Toluene was distilled off under reduced pressure to get the crude product. The crude product was dissolved in toluene (35 ml), hexane (200 ml) was added and the mixture cooled at 0° C. The solid product so obtained was filtered and dried to give 14.0 g of the title compound (Yield: 73%, HPLC Purity 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148355B2
Source datasetuspto-grants-2006_12
ORD IDord-f8329fcb31f64a37ba5427f9c5fdadb5
Source noteuspto-grants-2006_12