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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095960Generated: October 29, 2026

Hydrochloride methanol → N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)-3-fluorophenyl]-6-methyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxamide hydrochloride

https://huagongshe.com/reaction/2095960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
ReactantN-(4-((2-((cyclopropylcarbonyl)amino)imidazo(1,2-a)pyridin-6-yl)oxy)-3-fluorophenyl)-6-methyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxamideHCID 44595039—
ProductN-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)-3-fluorophenyl]-6-methyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxamide hydrochlorideHCID 6696888679%

Reaction Steps

A solution (5 to 10%) of hydrogen chloride/methanol was heated to 50° C., and N-[4-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)-3-fluorophenyl]-6-methyl-2-oxo-1-phenyl-1,2-dihydropyridine-3-carboxamide (500 mg, 0.93 mmol) was added. The mixture was stirred for 5 min and at room temperature for 30 min. The precipitate was collected by filtration and washed with methanol to give the title compound (420 mg, 79%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445509B2
Source datasetuspto-grants-2013_05
ORD IDord-f8c0be460739408cbb5e57dbdb4a8ea5
Source noteuspto-grants-2013_05