Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704413Generated: October 28, 2026

Dicyclohexylcarbodiimide → HCID 20074099, compound

https://huagongshe.com/reaction/704413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-HeptylpiperazineHCID 2736510—
ReactantHCID 67934630HCID 67934630—
SolventDimethylformamideHCID 6228—
ProductHCID 20074099HCID 2007409968.4%

Reaction Steps

A mixture of 1.15 g of 2-(3-pyridyl)-1-pyrroline-4-carboxylic acid monohydrobromide, 770 mg of 1-heptylpiperazine, 860 mg of dicyclohexylcarbodiimide and 560 mg of 1-hydroxybenzotriazole in 15 ml of N,N-dimethylformamide was stirred at room temperature for 3 days. After dilution of the reaction mixture with ethyl acetate, the insoluble matter was filtered off, the filtrate was concentrated under reduced pressure and, after addition of 0.5N aqueous sodium hydroxide, the residue was extracted with ethyl acetate. The organic layer was extracted with 1N hydrochloric acid. The aqueous layer was adjusted to pH 10 by addition of potassium carbonate and extracted again with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (15 g). Elution with ethyl acetate gave 1.01 g of 1-heptyl-4-[2-(3-pyridyl)-2-pyrrolin-5-ylcarbonyl]piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987132
Source datasetuspto-grants-1991_01
ORD IDord-e95557482fc64ef3bc6219fb5a456482
Source noteuspto-grants-1991_01