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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331213Generated: October 29, 2026

Water → Cabozantinib

https://huagongshe.com/reaction/331213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
Reactant1-[(4-Fluorophenyl)carbamoyl]cyclopropanecarbonyl chlorideHCID 58083267—
SolventTetrahydrofuranHCID 8028—
ProductCabozantinibHCID 25102847—

Reaction Conditions

Temperature22.5 °C

Reaction Steps

The solution from the previous step containing 1-(4-fluoro-phenylcarbamoyl)-cyclopropanecarbonyl chloride was added to a mixture of 4-(6,7-dimethoxy-quinoline-4-yloxy)-phenylamine (3.0 kg) and potassium carbonate (4.0 kg) in THF (27.0 kg) and water (13.0 kg) at a rate such that the batch temperature did not exceed 30° C. When the reaction was complete (in typically 10 minutes), water (74.0 kg) was added. The mixture was stirred at 15-30° C. for approximately 10 hours, which resulted in the precipitation of the product. The product was recovered by filtration, washed with a premade solution of THF (11.0 kg) and water (24.0 kg), and dried at approximately 65° C. under vacuum for approximately 12 hours to afford the title compound (free base, 5.0 kg). 1H NMR (400 MHz, d6-DMSO): δ 10.2 (s, 1H), 10.05 (s, 1H), 8.4 (s, 1H), 7.8 (m, 2H), 7.65 (m, 2H), 7.5 (s, 1H), 7.35 (s, 1H), 7.25 (m, 2H), 7.15 (m, 2H), 6.4 (s, 1H), 4.0 (d, 6H), 1.5 (s, 4H). LC/MS: M+H=502.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877776B2
Source datasetuspto-grants-2014_11
ORD IDord-954002d8875b48e2b4619c93852b9b87
Source noteuspto-grants-2014_11