Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183151Generated: October 30, 2026

1,2-Dichloroethane → 1-[(4-Fluorophenyl)carbamoyl]cyclopropanecarboxylic Acid

https://huagongshe.com/reaction/1183151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-FluoroanilineHCID 9731—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-(Methoxycarbonyl)cyclopropane-1-carboxylic acidHCID 13861823—
SolventDichloromethaneHCID 6344—
Product1-[(4-Fluorophenyl)carbamoyl]cyclopropanecarboxylic AcidHCID 2108153043%

Reaction Steps

To a mixture of 1-(methoxycarbonyl)cyclopropanecarboxylic acid (4.2 g) and 4-fluoroaniline (3.3 g) in DCM (40 ml) was added EDC (7.4 g) and HOBt (4 g), the reaction was stirred at RT for 4 hours and washed with 1N HCl, NaHCO3 solution, water, brine and dried over Na2SO4. The solution was evaporated and the residue was mixed with NaOH (3.2 g) and MeOH/H2O (60 ml/6 ml). The mixture was refluxed for 30 minutes then was evaporated. The residue was acidified with 4N HCl and the precipitate was filtered. The filter cake was washed with water followed by cold EtOH to give the product as 1-(4-fluorophenylcarbamoyl)-cyclopropanecarboxylic acid 2.8 g. This product (1.8 g) was mixed with DCM (30 ml) and two drops of DMF. Oxalyl chloride (1.2 ml) was added into the solution and the reaction was refluxed for one hour. The solvent was removed followed by adding DCM (20 ml) and DIPEA (1.3 ml). To the above solution was added 4-methoxybenzyl 1-((4-(2-fluoro-4-aminophenoxy)-6-methoxyquinolin-7-yloxy)-methyl)cyclopropylcarbamate (1.5 g), the reaction was stirred at RT for 4 hours. Saturated NaHCO3 (30 ml) and DCM (80 ml) were added into the reaction, the solution was further extracted with DCM twice. The combined organic layer was washed with water, brine and dried over Na2SO4. The solution was evaporated and purified with silica gel column to give the titled compound 2.1 gram. Mass: (M+1), 739

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664244B2
Source datasetuspto-grants-2014_03
ORD IDord-48add35bbd2040f0804564e2d74424f9
Source noteuspto-grants-2014_03