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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609713Generated: October 29, 2026

Dimethylcarbamoyl Chloride → HCID 18396082, compound

https://huagongshe.com/reaction/609713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
Reactant(2R)-Piperazine-2-carboxylic acid--hydrogen chloride (1/2)HCID 12680090—
ReactantHCID 86754904HCID 86754904—
SolventAcetonitrileHCID 6342—
SolventHexamethyldisilazaneHCID 13838—
ProductHCID 18396082HCID 1839608270.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

Piperazine-2(R)-carboxylic acid dihydrochloride (5.0 g, 24.6 mmol) was suspended in hexamethyldisilazane (50 ml). The reaction mixture was heated at about 120° C. to achieve complete dissolution and then cooled to about 80° C. A solution of dimethylcarbamoyl chloride (3.18 g, 29.5 mmol) in acetonitrile (5 ml) was added and the reaction mixture is stirred overnight at about 80° C. A solution of 4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridine sulfamoyl chloride (5.4 g, 19.58 mmol) in acetonitrile (10 ml) was added and the resulting reaction mixture was stirred at about 80° C. till the completion of the reaction (followed by HPLC). The reaction mixture was cooled and then quenched with methanol. The resulting slurry was concentrated and then replaced into water. The aqueous slurry was made alkaline with ammonium hydroxide and then washed with dichloromethane. The aqueous phase was acidified with dilute HCl and extracted with dichoromethane. The organic extracts were washed with water and then evaporated to dryness to yield 4-(N,N-dimethylaminocarbonyl)-1-[4-(4-fluoropheny)-1,2,3,6-tetrahydropyridinesulfonyl]piperazine-2(R)-carboxylic acid (6.1 g) as a beige colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998412
Source datasetuspto-grants-1999_12
ORD IDord-c25214ecf6504ec383f173ad9233e023
Source noteuspto-grants-1999_12