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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986978Generated: November 1, 2026

Dimethyl Sulfoxide → Lenvatinib

https://huagongshe.com/reaction/1986978

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

In a reaction vessel were placed 7-methoxy-4-chloroquinoline-6-carboxamide (5.00 kg, 21.13 mol), dimethylsulfoxide (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) in that order, under a nitrogen atmosphere. After stirring at 20° C. for 30 min, the temperature was raised to 65° C. over a period of 2.5 hours. After stirring at the same temperature for 19 hours, 33% (v/v) acetone water (5.0 L) and water (10.0 L) were added dropwise over a period of 3.5 hours. Upon completion of the dropwise addition, the mixture was stirred at 60° C. for 2 hours, and 33% (v/v) acetone water (20.0 L) and water (40.0 L) were added dropwise at 55° C. or higher over a period of 1 hour. After then stirring at 40° C. for 16 hours, the precipitated crystals were collected by filtration using a nitrogen pressure filter, and the crystals were 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 (96.3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550483B2
Source datasetuspto-grants-2009_06
ORD IDord-3661b2bc26084d8dbc667e625d150b0e
Source noteuspto-grants-2009_06