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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572628Generated: October 31, 2026

Ethanolamine → N-[4-cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-yl-2-thienyl]-N-(2-hydroxyethyl)urea

https://huagongshe.com/reaction/572628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantTolueneHCID 1140—
ReactantTetrahydrofuranHCID 8028—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-Cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-ylthiophene-2-carboxylic acidHCID 44155665—
ProductN-[4-cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-yl-2-thienyl]-N-(2-hydroxyethyl)ureaHCID 68639607—

Reaction Steps

4-cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-ylthiophene-2-carboxylic acid (0.030 g, 0.08 mmol) was weighed out into a microwave tube that was then sealed. Toluene (1 ml), TEA (0.014 mL, 0.100 mmol) and diphenylphosphoryl azide (0.020 mL, 0.091 mmol) were added to the tube. The reaction mixture was shaken at room temperature for 30 minutes, and then heated to 80° C. for 2 hours. 2-aminoethanol (0.0061 ml, 0.1 mmol) and anhydrous THF (1 mL) and TEA (0.014 mL, 0.100 mmol) were pre-mixed and then added to the reaction mixture. The reaction was heated at 80° C. for a further 60 minutes, then allowed to cool to RT and shaken overnight. The solvent was evaporated in a Genevac HT12 and the residue was purified on the Agilent 100 series LC/MSD (FA) to give N-[4-cyano-3-(2,4-dichlorophenyl)-5-morpholin-4-yl-2-thienyl]-N-(2-hydroxyethyl)urea (86). LCMS: (FA) ES+ 441.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029411B2
Source datasetuspto-grants-2015_05
ORD IDord-fbe0fc07be5f4b309e8fe81666265701
Source noteuspto-grants-2015_05