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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160735Generated: November 1, 2026

Diisopropylethylamine → 2-Methyl-N-[1-methyl-3-(4-methylphenyl)-2-phenylpropyl]-2-{[5-(trifluoromethyl)pyridin-2-yl]oxy}propanamide

https://huagongshe.com/reaction/1160735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
Reactant2-Methyl-2-(5-(trifluoromethyl)pyridin-2-yloxy)propanoic acidHCID 16098342—
Reactant4-(4-Methylphenyl)-3-phenylbutan-2-amineHCID 22270653—
SolventDichloromethaneHCID 6344—
Product2-Methyl-N-[1-methyl-3-(4-methylphenyl)-2-phenylpropyl]-2-{[5-(trifluoromethyl)pyridin-2-yl]oxy}propanamideHCID 22270600—

Reaction Steps

To a solution of 2-methyl-2-{[5-(trifluoromethyl)pyridin-2-yl]oxy}propanoic acid (Reference example 55, 250 mg, 1.04 mmol) and 4-(4-methylphenyl)-3-phenylbutan-2-amine (Reference example 102, 260 mg, 1.04 mmol, mixture of 4 isomers) in CH2Cl2 (5.5 mL) at RT was added diisopropylethylamine (272 μl, 1.56 mmol) followed by PyBOP (649 mg, 1.25 mmol) and the reaction mixture stirred overnight. The reaction was purified by loading the reaction mixture directly onto a silica gel column and eluting from 0-30% EtOAc/hexane to give the title compound as a mixture of 4 isomers. The diastereomers were separated by HPLC on a ZORBAX RxSi column eluting 97% hexane: 3% ethanol at 20 mL/min with retention times of:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816534B2
Source datasetuspto-grants-2010_10
ORD IDord-e993a46de7eb4510afe70150f70692e3
Source noteuspto-grants-2010_10