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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095961Generated: November 2, 2026

Diethyl Ether → 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 methanesulfonate

https://huagongshe.com/reaction/2095961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantMethanesulfonic AcidHCID 6395—
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—
SolventEthanolHCID 702—
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 methanesulfonateHCID 8665140293.3%

Reaction Steps

A suspension (3 mL) of 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) in ethanol was heated to 80° C., and a solution (1 mL) of methanesulfonic acid (107 mg, 1.12 mmol) in ethanol was added. The mixture was cooled to room temperature, diethyl ether was added dropwise, and the obtained solid was collected by filtration to give the title compound (550 mg, 93%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445509B2
Source datasetuspto-grants-2013_05
ORD IDord-37ff2842c54446c195cf0e6a28256a2f
Source noteuspto-grants-2013_05