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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885406Generated: November 1, 2026

Dicyclohexylcarbodiimide → HCID 14772799, compound

https://huagongshe.com/reaction/1885406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-((Pyrrolidine-1-carbonyl)methyl)piperazineHCID 100614—
Reactant2-(3-Piridyl)thiazolidine-4-carboxylic acidHCID 327593—
SolventDimethylformamideHCID 6228—
ProductHCID 14772799HCID 1477279959.1%

Reaction Steps

To a solution of 2-(3-pyridyl)thiazolidine-4-caroxylic acid 2.1 g, 1-(pyrrolidinecarbonylmethyl)piperazine 1.8 g, 1-hydroxybenzotriazole 1.5 g and N,N-dimethylformamide 50 ml was added dicyclohexylcarbodiimide 2 g under ice-cooling, and the mixture was stirred overnight at room temperature. The resultant dicyclohexylurea was filtered off and the filtrate concentrated under reduced pressure. To the residue were added ethyl acetate 100 ml and water 10 ml, the mixture was basified by addition of sodium carbonate, sodium chloride added until saturation and allowed to stand. The organic layer was separated, washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with a mixture solution of ethyl acetate -methanol (6:4) to give 2.1 g of 1-[2-(3-pyridyl)thiazolidine-4-ylcarbonyl]-4-[1-(pyrrolidinyl)carbonylmethyl]piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05144035
Source datasetuspto-grants-1992_09
ORD IDord-108450279efa49d9989f03225016eb81
Source noteuspto-grants-1992_09