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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889710Generated: October 31, 2026

Cesium carbonate → 2-{5-[1-(1-Ethyl-propyl)-piperidin-3-yl]-4'-trifluoromethyl-biphenyl-3-yl}-4-methyl-pentanoic acid ethyl ester

https://huagongshe.com/reaction/889710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-Methyl-2-(5-piperidin-3-yl-4'-trifluoromethyl-biphenyl-3-yl)-pentanoic acid ethyl esterHCID 57666020—
Reactant1-iodo-3-BromopentaneHCID 86629850—
SolventAcetonitrileHCID 6342—
Product2-{5-[1-(1-Ethyl-propyl)-piperidin-3-yl]-4'-trifluoromethyl-biphenyl-3-yl}-4-methyl-pentanoic acid ethyl esterHCID 5766596775%

Reaction Conditions

Temperature78 °C

Reaction Steps

To a solution of compound 33b, 4-Methyl-2-(5-piperidin-3-yl-4′-trifluoromethyl-biphenyl-3-yl)-pentanoic acid ethyl ester (42 mg, 0.093 mmol) in CH3CN (0.5 ml) was added 1-iodo-3-Bromopentane (21.0 mg, 0. 14 mmol) and cesium carbonate (61.0 mg, 0.186 mmol). The reaction was heated to 78° C. overnight. The subsequent addition of the reactants as described above and allowing the reaction to continue over a second night, resulted in ˜75% product: starting material. The reaction was cooled to room temperature, concentrated in vacuo, diluted with EtOAc, washed with NaHCO3, and brine. The solution was filtered, and concentrated, then purified via silica gel chromatography to give the product as a clear oil. (32.7 mg, 68% ) Calculated for C31H42F3NO2 (M+H) 517.67, Found 518.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252935B2
Source datasetuspto-grants-2012_08
ORD IDord-bc1a46842fbd44fba38a6d65b6cdb7f6
Source noteuspto-grants-2012_08