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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167107Generated: October 25, 2026

Triethylamine → Methyl 2-methyl-2-phenyl-5-{4-[(biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-pentanecarboxylate

https://huagongshe.com/reaction/1167107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-[(2-Biphenyl)carbonylamino]piperidineHCID 11391851—
ReactantMethyl 5-bromo-2-methyl-2-phenyl-pentanecarboxylateHCID 22995606—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-methyl-2-phenyl-5-{4-[(biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-pentanecarboxylateHCID 22995520—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 0.634 g (0.002 mol) of biphenyl-2-carboxylic acid-piperidin-4-ylamide, 0.5 g (1.75 mmol) of methyl 5-bromo-2-methyl-2-phenyl-pentanecarboxylate and 1 ml (0.007 mol) of triethylamine are dissolved in 3 ml dimethylformamide. The mixture is stirred for 14 hours at 80° C. Then the reaction mixture is poured onto water and extracted with ethyl acetate. The organic phase is dried over sodium sulphate. After column chromatography on silica gel (eluant: dichloromethane/methanol=10:1) colourless crystals remain.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617325B1
Source datasetuspto-grants-2003_09
ORD IDord-be0aaedc435e4e1c9fd25e02e5d8de5a
Source noteuspto-grants-2003_09