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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265649Generated: October 30, 2026

HCID 23152981, compound → HCID 59596927, compound

https://huagongshe.com/reaction/2265649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23152981HCID 23152981—
Reactant[4-(3-fluoro-4-{[1-(4-fluorophenylcarbamoyl)cyclopropanecarbonyl]amino}phenoxy)pyridin-2-yl]-N-(phenoxycarbonyl)carbamic acid phenyl esterHCID 59597026—
SolventDimethylformamideHCID 6228—
ProductHCID 59596927HCID 5959692765.9%

Reaction Steps

To a solution of phenyl N-[4-(3-fluoro-4-{[1-(4-fluorophenylcarbamoyl)cyclopropanecarbonyl]amino}phenoxy)pyridin-2-yl]-N-phenoxycarbonylcarbamate (50.0 mg) in N,N-dimethylformamide (2.0 ml) was added N-[1-(2-dimethylaminoethyl)piperidin-4-yl]-N-methylamine (69.5 mg), followed by stirring at room temperature for 22 hr. The reaction mixture was partitioned between ethyl acetate and a 1N aqueous solution of sodium hydroxide. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was removed, and the residue was purified by silica gel column chromatography (Fuji Silysia NH, ethyl acetate, then ethyl acetate:methanol=20:1). Fractions containing the target compound were concentrated. To the residue was added diethyl ether:hexane=1:3, and the precipitate was collected by filtration. This was washed with hexane and dried under aeration to provide the titled compound as white powder (31.4 mg, 65.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855290B2
Source datasetuspto-grants-2010_12
ORD IDord-0c3d5759eb364f1bb562de8a7e647d28
Source noteuspto-grants-2010_12