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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066245Generated: November 1, 2026

(3S)-(-)-3-(Dimethylamino)pyrrolidine → N-(4-{[2-({[(3S)-3-(Dimethylamino)pyrrolidin-1-yl]carbonyl}amino)pyridin-4-yl]oxy}-2-fluorophenyl)-N'-phenylcyclopropane-1,1-dicarboxamide

https://huagongshe.com/reaction/2066245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3S)-(-)-3-(Dimethylamino)pyrrolidineHCID 7019156—
Reactantphenyl N-[4-(3-fluoro-4-{[1-(phenylcarbamoyl)cyclopropanecarbonyl]amino}phenoxy)pyridin-2-yl]-N-phenoxycarbonylcarbamateHCID 59596979—
SolventDimethylformamideHCID 6228—
ProductN-(4-{[2-({[(3S)-3-(Dimethylamino)pyrrolidin-1-yl]carbonyl}amino)pyridin-4-yl]oxy}-2-fluorophenyl)-N'-phenylcyclopropane-1,1-dicarboxamideHCID 59596901—

Reaction Steps

To a solution of phenyl N-[4-(3-fluoro-4-{[1-(phenylcarbamoyl)cyclopropanecarbonyl]amino}phenoxy)pyridin-2-yl]-N-phenoxycarbonylcarbamate (50.0 mg) in N,N-dimethylformamide (1.0 ml) was added (3S)-(−)-3-dimethylaminopyrrolidine (44 mg), followed by stirring at room temperature for 3.5 hr. The reaction mixture was partitioned between ethyl acetate and 1N sodium hydroxide. The organic layer was washed with brine, and dried over anhydrous sodium sulfate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288538B2
Source datasetuspto-grants-2012_10
ORD IDord-df2cdb223a0d4fb09dd7b1016b7061b7
Source noteuspto-grants-2012_10