Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869491Generated: October 26, 2026

Dimethyl Sulfoxide → Lenvatinib

https://huagongshe.com/reaction/869491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant4-Chloro-7-methoxyquinoline-6-carboxamideHCID 22936418—
ReactantME-92HCID 23135084—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventPropan-2-one--water (1/1)HCID 18366337—
ProductLenvatinibHCID 982382096.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

7-Methoxy-4-chloroquinoline-6-carboxamide (5.00 kg, 21.13 mol), dimethyl sulfoxide (55.05 kg), 1-(2-chloro-4-hydroxyphenyl)-3-cyclopropylurea (5.75 kg, 25.35 mol) and potassium t-butoxide (2.85 kg, 25.35 mol) were introduced in this order into a reaction vessel under a nitrogen atmosphere. The mixture was stirred for 30 min at 20° C., and the temperature was raised to 65° C. over 2.5 hours. The mixture was stirred at the same temperature for 19 hours. 33% (v/v) acetone-water (5.0 L) and water (10.0 L) were added dropwise over 3.5 hours. After the addition was completed, the mixture was stirred at 60° C. for 2 hours. 33% (v/v) acetone-water (20.0 L) and water (40.0 L) were added dropwise at 55° C. or more over 1 hour. After stirring at 40° C. for 16 hours, precipitated crystals were collected by filtration using a nitrogen pressure filter, and was washed with 33% (v/v) acetone-water (33.3 L), water (66.7 L), and acetone (50.0 L) in that order. The obtained crystals were dried at 60° C. for 22 hours using a conical vacuum dryer to give 7.78 kg of the titled compound (yield: 96.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969379B2
Source datasetuspto-grants-2015_03
ORD IDord-62a90b60afbd4ec3b427d78a3cba5011
Source noteuspto-grants-2015_03