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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63716Generated: October 26, 2026

2,6-Dichlorobenzoyl chloride → (S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester

https://huagongshe.com/reaction/63716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-N-((1,1-dimethylethoxy)carbonyl)-L-phenylalanine methyl esterHCID 11011855—
SolventDichloromethaneHCID 6344—
Product(S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl esterHCID 5439386188.5%

Reaction Steps

To a solution of (S)-3-[4-aminophenyl]-2-tert-butoxycarbonylamino-propionic acid methyl ester (37.57 g, 127.6 mmol) and 2,6-dichlorobenzoyl chloride (29.45 g, 140.6 mmol) in dichloromethane (350 mL) was added DIPEA (24.8 g, 192 mmol) at room temperature. The brown solution was stirred for 15 h at room temperature to afford a white suspension at this time TLC analysis of the mixture indicated the absence of starting material. Then, the solids were collected by filtration and the solids were washed with dichloromethane (150 mL) and air dried to obtain 52.75 g (88.4% yield) of (S)-2-tert-butoxycarbonylamino-3-[4-(2,6-dichlorobenzoylamino)phenyl]propionic acid methyl ester as a white solid: mp 192-194° C. ES(+)-HRMS m/e calcd. for C22H24Cl2N2O5 (M+H)+ 466.1062, obsd. 466.1069.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447035B2
Source datasetuspto-grants-2016_09
ORD IDord-ec259c0dcfa745ae80aa81e4c827b872
Source noteuspto-grants-2016_09