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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409932Generated: October 30, 2026

4-Methylmorpholine → 1-[4-(2-Carbamoylpyridin-4-yloxy)-2-fluorophenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester

https://huagongshe.com/reaction/409932

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantThionyl ChlorideHCID 24386—
Reactant1-(Benzyloxycarbonyl)cyclopropanecarboxylic acidHCID 57470860—
Reactant4-(4-Amino-3-fluorophenoxy)pyridine-2-carboxyamideHCID 131731635—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-[4-(2-Carbamoylpyridin-4-yloxy)-2-fluorophenylcarbamoyl]cyclopropanecarboxylic acid benzyl esterHCID 24788499—

Reaction Steps

Thionyl chloride was added at −20° C. to a solution of 1-(benzyloxycarbonyl)cyclopropanecarboxylic acid (97.98 g) in tetrahydrofuran (200 ml) and N-methylpyrrolidone (200 ml) and stirred for 30 minutes. A solution of 4-(4-amino-3-fluorophenoxy)pyridine-2-carboxyamide (100 g) and N-methylmorpholine (40.91 g) in N-methylpyrrolidone (600 ml) were added to the reaction mixture at the same temperature and stirred for 1 hour at 10° C. Water (100 g) was added to the reaction mixture and stirred for 1 hour at 20° C. After confirming the crystal precipitation, a 1N sodium hydroxide aqueous solution (1 L) was added and further stirred for 19 hours. The precipitated solid was collected by filtration and washed with water (500 g). The obtained solid was dried for 20 hours at 60° C. to give 176.7 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759530B2
Source datasetuspto-grants-2014_06
ORD IDord-f5229ec57e0440a398aace9b2b83cb4b
Source noteuspto-grants-2014_06