Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374839Generated: October 28, 2026

Triethylamine → N-[2-[4-(5H-dibenzo[a,d] [7]annulen-5-ylidene)-1-piperidinyl]-1-(hydroxymethyl)-2-oxoethyl]-1-piperidinecarboxamide

https://huagongshe.com/reaction/2374839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(5H-Dibenzo(a,d)cyclohepten-5-ylidene)piperidineHCID 159718—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-Hydroxy-2-[(1-piperidinylcarbonyl)amino]propionic acidHCID 61183027—
SolventDichloromethaneHCID 6344—
ProductN-[2-[4-(5H-dibenzo[a,d] [7]annulen-5-ylidene)-1-piperidinyl]-1-(hydroxymethyl)-2-oxoethyl]-1-piperidinecarboxamideHCID 59853888—

Reaction Steps

64.0 mg (0.296 mmol) of 3-hydroxy-2-[(1-piperidinylcarbonyl)amino]propionic acid, 80.9 mg (0.296 mmol) of 4-(5H-dibenzo[a,d][7]annulen-5-ylidene)piperidine and 85.1 mg (0.444 mmol) of 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide hydrochloride were dissolved in 10 ml of dichloromethane. 0.091 ml (0.651 mmol) of triethylamine was added to the obtained solution, and they were stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure. Ethyl acetate was added to the residue. After washing with saturated aqueous sodium chloride solution, the reaction product was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resultant product was purified by the silica gel chromatography (dichloromethane:methanol=9:1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462630B2
Source datasetuspto-grants-2008_12
ORD IDord-836917d5240b4b7f87f6f6dbacc1f851
Source noteuspto-grants-2008_12