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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035846Generated: October 26, 2026

1-(1-Methyl-4-piperidinyl)piperazine → 5-Cyano-3-(2-ethoxypyridin-3-yl)-6-fluoro-2-oxo-2,3-dihydro-1H-indol-3-yl 4-(1-methylpiperidin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1035846

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Methyl-4-piperidinyl)piperazineHCID 566324—
ReactantPhenyl 5-cyano-3-(2-ethoxypyridin-3-yl)-6-fluoro-2-oxo-3-phenoxycarbonyloxy-2,3-dihydroindole-1-carboxylateHCID 67087492—
SolventTetrahydrofuranHCID 8028—
Product5-Cyano-3-(2-ethoxypyridin-3-yl)-6-fluoro-2-oxo-2,3-dihydro-1H-indol-3-yl 4-(1-methylpiperidin-4-yl)piperazine-1-carboxylateHCID 6708768657%

Reaction Steps

A mixture of 291 mg (0.53 mmol) of phenyl 5-cyano-3-(2-ethoxypyridin-3-yl)-6-fluoro-2-oxo-3-phenoxycarbonyloxy-2,3-dihydroindole-1-carboxylate, 289 mg (1.58 mmol) of 1-(1-methylpiperidin-4-yl)piperazine and 6 ml of dried tetrahydrofuran (THF) was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure and stirred with methanol. The precipitated solid was filtered off and dried in a vacuum drying oven. 158 mg of the title compound were obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546401B2
Source datasetuspto-grants-2013_10
ORD IDord-c05d0492587d4c5199194115d3dee79f
Source noteuspto-grants-2013_10