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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517830Generated: November 3, 2026

Maleic Acid → (R)-1-(4-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenylcarbamoyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydropyrazol-1-yl)propan-2-yl 2-(methylamino)acetate maleate

https://huagongshe.com/reaction/1517830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AcidHCID 444266—
Reactant(R)-1-(4-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenylcarbamoyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydropyrazol-1-yl)propan-2-yl 2-(methylamino)acetateHCID 46937772—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product(R)-1-(4-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenylcarbamoyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydropyrazol-1-yl)propan-2-yl 2-(methylamino)acetate maleateHCID 66669919—

Reaction Steps

To a solution (R)-1-(4-(4-(7-methoxyquinolin-4-yloxy)-3-fluorophenylcarbamoyl)-2,3-dihydro-5-methyl-3-oxo-2-phenylpyrazol-1-yl)propan-2-yl 2-(methylamino)acetate (82.3 mg, 0.134 mmol) in a mixture of EtOAc (10 mL) and MeOH (10 mL) was added maleic acid (31.1 mg, 0.268 mmol, Shanghai San'aisi Reagent Co., Ltd). After stirring for 40 min, the reaction mixture was concentrated in vacuo. The residue was recrystallized in a mixture of MeOH (2 mL)/EtOAc (10 mL). The solid was collected by filtration, washed with EtOAc (5 mL×3) and dried under vacuum overnight. The title compound was obtained as a yellow solid (60.2 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232294B2
Source datasetuspto-grants-2012_07
ORD IDord-dcb1404c1929457f9fe2d4377705c319
Source noteuspto-grants-2012_07