Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040441Generated: October 30, 2026

1-(1-Methyl-4-piperidinyl)piperazine → 4-(1-Methyl-piperidin-4-yl)-piperazine-1-carboxylic acid [3-(2-ethoxy-phenyl)-5-methoxy-2-oxo-2,3-dihydro-1H-indol-3-yl]-amide

https://huagongshe.com/reaction/2040441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Methyl-4-piperidinyl)piperazineHCID 566324—
Reactant[3-(2-Ethoxy-phenyl)-5-methoxy-2-oxo-2,3-dihydro-1H-indol-3-yl]-carbamic acid phenyl esterHCID 57517779—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Methyl-piperidin-4-yl)-piperazine-1-carboxylic acid [3-(2-ethoxy-phenyl)-5-methoxy-2-oxo-2,3-dihydro-1H-indol-3-yl]-amideHCID 5751778065.7%

Reaction Steps

1.9 g (4.5 mmol) of the intermediate from Step D and 1.75 g (9.5 mmol) 1-(1-methylpiperidine-4-yl)-piperazine were dissolved in 30 ml dry THF and refluxed for 90 minutes. The volatiles were removed in vacuo. The resulting residue was dissolved in ethyl acetate, washed with H2O and dried over magnesium sulfate and the solvent was removed in vacuo. The residue was treated with H2O and the resulting precipitate was separated to yield 1.5 g of the intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580842B2
Source datasetuspto-grants-2013_11
ORD IDord-f20e93a1f2294adfa23c4f3fe5f3d9dd
Source noteuspto-grants-2013_11