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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197339Generated: October 30, 2026

Diisopropylethylamine → (2'-{[(3,5-Dichloro-benzyloxycarbonyl)-ethyl-amino]-methyl)-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid methyl ester

https://huagongshe.com/reaction/2197339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3,5-Dichlorobenzyl ChloroformateHCID 13305532—
Reactant(2'-Ethylaminomethyl-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid methyl esterHCID 66603748—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(2'-{[(3,5-Dichloro-benzyloxycarbonyl)-ethyl-amino]-methyl)-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid methyl esterHCID 66604037—

Reaction Steps

To (2′-ethylaminomethyl-6-methoxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid methyl ester (0.101 g, 0.26 mmol) and diisopropylethylamine (0.23 mL, 1.32 mmol) in CH2Cl2 (1 mL) was added 3,5-dichlorobenzyl chloroformate (1.06 mmol) in CH2Cl2, and the reaction was stirred at room temperature for 5 minutes. The mixture was diluted with H2O and extracted with CH2Cl2. The combined organic layers were dried over Na2SO4, decanted, and concentrated, and the residue was purified by silica gel chromatography to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338484B2
Source datasetuspto-grants-2012_12
ORD IDord-60468c6647a24bf6b220182d3fefd9bc
Source noteuspto-grants-2012_12