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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201694Generated: October 28, 2026

Triethylamine → 3-(5-(Cyclopent-1-en-1-yl)-2-nitrophenyl)-1-methyl-1-propylurea

https://huagongshe.com/reaction/2201694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-MethylpropylamineHCID 12315—
ReactantTriphosgeneHCID 94429—
Reactant5-(Cyclopent-1-en-1-yl)-2-nitroanilineHCID 86712523—
SolventDichloromethaneHCID 6344—
Product3-(5-(Cyclopent-1-en-1-yl)-2-nitrophenyl)-1-methyl-1-propylureaHCID 7098176575.7%

Reaction Steps

To a solution of 5-(cyclopent-1-en-1-yl)-2-nitroaniline (0.13 g, 0.61 mmol, 1.0 equiv.) in dichloromethane were added triethylamine (0.68 mL, 4.90 mmol, 8.0 equiv.) and triphosgene (0.18 g, 0.61 mmol, 1.0 equiv.) at 0° C. The mixture was warmed to room temperature and stirred for 3 h at room temperature. Triethylamine (0.17 mL, 1.22 mmol, 2.0 equiv.) and N-methylpropan-1-amine (0.07 g, 0.92 mmol, 1.5 equiv.) were added slowly to the reaction mixture. The reaction mixture was slowly warmed to 50° C. and stirred for 2 h. The mixture was diluted with dichloromethane, washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give crude 3-(5-(cyclopent-1-en-1-yl)-2-nitrophenyl)-1-methyl-1-propylurea (0.14 g, 76% crude yield) which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365498B2
Source datasetuspto-grants-2016_06
ORD IDord-0e71b9418bb241a8a203dc88275baa07
Source noteuspto-grants-2016_06