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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133086Generated: October 30, 2026

Ethylmorpholine → 3-(4-chlorophenyl)-N-(2,2-diethoxyethyl)-N-isopropyl-2-[3-(4-methoxybenzenesulfonylamino)propionylamino]propionamide

https://huagongshe.com/reaction/133086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-(4-Methoxybenzenesulfonamido)propanoic acidHCID 757377—
Reactant2-amino-3-(4-chlorophenyl)-N-(2,2-diethoxyethyl)-N-isopropylpropionamideHCID 67341646—
Solvent1,2-DichloroethaneHCID 11—
SolventDimethylformamideHCID 6228—
Product3-(4-chlorophenyl)-N-(2,2-diethoxyethyl)-N-isopropyl-2-[3-(4-methoxybenzenesulfonylamino)propionylamino]propionamideHCID 68452840—

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 3-(4-methoxybenzenesulfonylamino)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 mixture 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 with Chromabond XTR 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=598.16 (calculated); measured value (M−C2H6O+H)+: 552.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390814B2
Source datasetuspto-grants-2008_06
ORD IDord-c7b9a3523c92451e9f69af6bb8d821d6
Source noteuspto-grants-2008_06