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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843030Generated: October 30, 2026

Dimethylcarbamoyl Chloride → HCID 18396082, compound

https://huagongshe.com/reaction/843030

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-fluorophenyl)-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 numberUS06376506B1
Source datasetuspto-grants-2002_04
ORD IDord-d33e76bf3e904f60903b90de831be97c
Source noteuspto-grants-2002_04