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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433132Generated: October 27, 2026

Ethanol → Lenvatinib

https://huagongshe.com/reaction/1433132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantCyclopropylamineHCID 69828—
Reactant(4-((6-(Aminocarbonyl)-7-methoxy-4-quinolinyl)oxy)-2-chlorophenyl)carbamic acid phenyl esterHCID 22936529—
SolventDimethylformamideHCID 6228—
ProductLenvatinibHCID 9823820—

Reaction Steps

Phenyl N-(4-(6-carbamoyl-7-methoxy-4-quinolyl)oxy-2-chlorophenyl)carbamate (17.5 g, 37.7 mmol) disclosed in WO 02/32872 was dissolved in N,N-dimethylformamide (350 mL), and then cyclopropylamine (6.53 mL, 94.25 mmol) was added to the reaction mixture under a nitrogen atmosphere, followed by stirring overnight at room temperature. To the mixture was added water (1.75 L), and the mixture was stirred. Precipitated crude crystals were filtered off, washed with water, and dried at 70° C. for 50 min. To the obtained crude crystals was added ethanol (300 mL), and then the mixture was heated under reflux for 30 min to dissolve, followed by stirring overnight to cool slowly down to room temperature. Precipitated crystals was filtered off and dried under vacuum, and then further dried at 70° C. for 8 hours to give the titled crystals (12.91 g; 80.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612208B2
Source datasetuspto-grants-2009_11
ORD IDord-b60d29f2f73a4e2ba2e5c3f7312651aa
Source noteuspto-grants-2009_11