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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381486Generated: November 2, 2026

Triethylamine → HCID 15887790, compound

https://huagongshe.com/reaction/381486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-Acetamidocinnamic acidHCID 5357155—
SolventDichloromethaneHCID 6344—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 15887790HCID 1588779051%

Reaction Steps

To a solution of Intermediate 1 (0.2 g, 0.81 mmol) in 40 mL of DCM were added Et3N (0.13 mL, 1.1 equiv.), DCC (0.18 g, 1.1 equiv.), HOBT (0.12 g , 1.1 equiv.) and (E)-3-(4-acetylaminophenyl)acrylic acid (0.18 g , 1.1 equiv.). After 24 hours of stirring at rt the reaction was judged to be completed by tlc monitoring (SiO2, DCM:MeOH 95:5) and was quenched with 150 mL of water. A white solid precipitated out and was filtered off. The filtrate was extracted with DCM, washed with brine (5 mL), dried over MgSO4 and concentrated in vacuo. Flash chromatography on a 2.5×25 cm2 column of silica gel using DCM:MeOH (98:2) as eluting solvent and removal of the solvent in vacuo gave the title compound (0.18 g, 51%) as yellow crystals after recrystallization from 2-propanol:pentane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306870B1
Source datasetuspto-grants-2001_10
ORD IDord-9ba7b5f799864c85942d49708ab47911
Source noteuspto-grants-2001_10