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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670499Generated: November 1, 2026

Ethylmorpholine → N-{2-(4-Chlorophenyl)-1-[(2,2-diethoxyethyl)isopropylcarbamoyl]ethyl}-3-(2,4-dichlorobenzenesulfonylamino)-2-methanesulfonylaminopropionamide

https://huagongshe.com/reaction/1670499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-Benzyloxycarbonylamino-3-(2,4-dichlorobenzenesulfonylamino)propionic acidHCID 67339404—
Reactant2-amino-3-(4-chlorophenyl)-N-(2,2-diethoxyethyl)-N-isopropylpropionamideHCID 67341646—
Solvent1,2-DichloroethaneHCID 11—
SolventDimethylformamideHCID 6228—
ProductN-{2-(4-Chlorophenyl)-1-[(2,2-diethoxyethyl)isopropylcarbamoyl]ethyl}-3-(2,4-dichlorobenzenesulfonylamino)-2-methanesulfonylaminopropionamideHCID 67340421—

Reaction Steps

52 mg of EDC, 45 mg of HOBt and 100 μl of N-ethylmorpholine are added to a solution of 124 mg of 2-benzyloxycarbonylamino-3-(2,4-dichlorobenzenesulfonylamino)propionic acid in 1 ml of DMF. A solution of 100 mg of 2-amino-3-(4-chlorophenyl)-N-(2,2-diethoxyethyl)-N-isopropylpropionamide in 1 ml of DMF is added dropwise thereto, and the solution is left to stir for 12 h. The reaction solution is filtered, mixed with ethyl acetate and then extracted with 5% aqueous sodium bicarbonate solution and aqueous sodium chloride solution. Drying of the organic phase over sodium sulfate is followed by concentration under reduced pressure, and the residue is separated by HPLC (Knauer Eurospher-100-10-C18, water (0.1% trifluoroacetic acid)/acetonitrile (0.1% trifluoroacetic acid)=80/20→10/90). The desired product is obtained with MW=784.186 (calculated); measured value (M−CO2+H)+: 741.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994168B2
Source datasetuspto-grants-2011_08
ORD IDord-682df87d12e9445f95ee9c28342716ee
Source noteuspto-grants-2011_08