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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095962Generated: November 1, 2026

Acetic Acid → N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)-3-fluorophenyl]-1-(4-fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxamide acetate

https://huagongshe.com/reaction/2095962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantN-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)-3-fluorophenyl]-1-(4-fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxamideHCID 44462744—
SolventWaterHCID 962—
ProductN-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)-3-fluorophenyl]-1-(4-fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxamide acetateHCID 6696888966%

Reaction Conditions

Temperature60 °C

Reaction Steps

To N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)-3-fluorophenyl]-1-(4-fluorophenyl)-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxamide (700 mg, 1.26 mmol) was added acetic acid (3.5 mL), and the mixture was heated to 60° C. Methylethylketone (2.1 mL) and water (3.5 mL) were added, and the mixture was cooled to room temperature and stirred at room temperature for 16 hr. The precipitate was collected by filtration and washed with water to give the title compound (512 mg, 66%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445509B2
Source datasetuspto-grants-2013_05
ORD IDord-3a5e1ff48ad64903ab5d7c3ab984736d
Source noteuspto-grants-2013_05