Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747047Generated: October 30, 2026

1,2-Dichloroethane → n-Cycloheptyl-2-(5,5-dimethyl-3-oxo-1-(2,4,6-trimethylbenzene-sulfonyl)piperazin-2(r,s)-yl)acetamide

https://huagongshe.com/reaction/747047

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantCycloheptylamineHCID 2899—
ReactantEthyl AcetateHCID 8857—
Reactant(5,5-Dimethyl-3-oxo-1-(2,4,6-trimethylbenzene-sulfonyl)piperazin-2-yl)acetic acidHCID 69078569—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Productn-Cycloheptyl-2-(5,5-dimethyl-3-oxo-1-(2,4,6-trimethylbenzene-sulfonyl)piperazin-2(r,s)-yl)acetamideHCID 11751607—

Reaction Steps

To (5,5-dimethyl-3-oxo-1-(2,4,6-trimethylbenzene-sulfonyl)piperazin-2-yl)acetic acid (0.32 g, 0.94 mmol) in DMF (3 mL) was added cycloheptyl amine (0.5 mL), EDC (0.5 g, 2.5 mmol), and DMAP (0.3 g, 2.6 mmol). The mixture was stirred at RT overnight. TLC indicated that the reaction was not complete. Additional EDC (0.3 g) was added and the mixture was heated at 65° C. for 1 h. The mixture was cooled to RT. EtOAc (80 mL) was added and mixture was washed with dilute HCl in brine. The EtOAc solution was dried and evaporated to give the crude compound. Column chromatograph purification (silica gel, 0-2% MeOH/CH2Cl2) gave the titled compound. MS: 464.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393852B2
Source datasetuspto-grants-2008_07
ORD IDord-2e9773d9906441bdbf2c66a05e69db29
Source noteuspto-grants-2008_07