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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427404Generated: October 29, 2026

1,2-Dichloroethane → n-{1-[(Benzyl-methyl-amino)-methyl]-1-cyano-3-phenyl-propyl}-2-cyclohexylmethyl-4-morpholin-4-yl-oxo-butyramide

https://huagongshe.com/reaction/427404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
ReactantHCID 18768971HCID 18768971—
Reactant2-Cyclohexylmethyl-4-morpholin-4-yl-oxo-butanoic acidHCID 18768987—
SolventDichloromethaneHCID 6344—
Productn-{1-[(Benzyl-methyl-amino)-methyl]-1-cyano-3-phenyl-propyl}-2-cyclohexylmethyl-4-morpholin-4-yl-oxo-butyramideHCID 1876894525%

Reaction Steps

2-Cyclohexylmethyl-4-morpholin-4-yl-oxo-butanoic acid (0.097 g, 0.34 mmol, 1.0 equiv) was dissolved in 10 mL of CH2Cl2 followed by addition of EDC (0.065 g, 0.34 mmol, 1.0 equiv). The solution was stirred for 15 min at which time a solution of 2-amino-2-[(benzyl-methyl-amino)-methyl]-4-phenyl-butyronitrile (0.10 g, 0.34 mmol, 1.0 equiv) in 5 mL of CH2Cl2 was added followed by N-methylmorpholine (0.137 g, 1.36 mmol, 4.0 equiv). The resulting solution was stirred at room temperature for 72 h. The volatiles were removed in vacuo and the residue was redissolved in 100 mL of EtOAc and the solution was washed 2×25 mL brine. The organic layer was evaporated to dryness and the crude product was purified by semi-prep reverse-phase HPLC using 40% CH3CN in water to 90% over a time of 25 min. The appropriate fractions were combined and concentrated to yield the desired product as a thick oil (0.047 g, 25%); MS, m/z 559=M+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313117B1
Source datasetuspto-grants-2001_11
ORD IDord-d863c1cb44cc4ad88b1c3723172ea9a8
Source noteuspto-grants-2001_11