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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852255Generated: October 27, 2026

Triethylamine → (S)-3-[4-(2,6-Dichlorobenzoylamino)phenyl]-2-{3-[2-(toluene-4-sulfonyl)-5-trifluoro methylphenyl]ureido}propionic acid methyl ester

https://huagongshe.com/reaction/852255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiphosgeneHCID 10426—
ReactantIsocyanateHCID 105034—
Reactant2-(4-Methylphenyl)sulfonyl-5-(trifluoromethyl)anilineHCID 2768165—
Reactantmethyl (2S)-2-amino-3-{4-[(2,6-dichlorobenzoyl)amino]phenyl}propionate hydrochlorideHCID 23383932—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product(S)-3-[4-(2,6-Dichlorobenzoylamino)phenyl]-2-{3-[2-(toluene-4-sulfonyl)-5-trifluoro methylphenyl]ureido}propionic acid methyl esterHCID 69375653163.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-(toluene-4-sulfonyl)-5-trifluoromethylphenylamine (0.2 g, 0.63 mmol) and diphosgene (0.061 g, 0.31 mmol) in dioxane (2 ml) was heated at 60° C. for 16 h. The solvent was removed under reduced pressure. The crude isocyanate was slowly added to a solution of (S)-2-amino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester hydrochloride (0.25 g, 0.63 mmol) and triethylamine (0.063 g, 0.63 mmol) in dichloromethane (2 ml) and the resulting reaction mixture was stirred at room temperature overnight. The precipitate obtained was collected by filtration, washed several times with dichloromethane and dried under vacuum to yield the title compound (0.36 g, 82%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253171B2
Source datasetuspto-grants-2007_08
ORD IDord-98bcc5831d584c3eab37773fb48e3440
Source noteuspto-grants-2007_08