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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709283Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 14772798, compound

https://huagongshe.com/reaction/1709283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-(2-Pyrimidinyl)piperazineHCID 88747—
Reactant2-(3-Piridyl)thiazolidine-4-carboxylic acidHCID 327593—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 14772798HCID 14772798—

Reaction Steps

To a solution of 2-(3-pyridyl)thiazolidine-4-carboxylic acid 2.1 g, 1-(2-pyrimidinyl)piperazine.2 hydrochyloride 2.2 g, triethylamine 1.8 g, 1-hydroxybenzotriazole 1.5 g and N,N-dimethylformamide 30 ml was added dicyclohexylcarbodiimide 2.0 g under cooling and the mixture was stirred overnight at room temperature. The resultant dicyclohexylurea was distilled off, ethyl acetate 100 ml and water 50 ml were added to the filtrate and the solution was basified by addition of potassium carbonate. The organic layer was separated and the aqueous layer extracted with ethyl acetate. The organic layer and extract were combined, washed successively with water and saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethanol to give 0.8 g of 1-[2-(3-pyridyl)thiazolidine-4-ylcarbonyl]-4-(2-pyrimidinyl)piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04948795
Source datasetuspto-grants-1990_08
ORD IDord-0b9991e131ed40b289e57f7325edbaaa
Source noteuspto-grants-1990_08