Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494915Generated: October 31, 2026

N-methyl-1-(1-benzyloxycarbonylpiperidin-4-yl)-1H-indole-6-carboxamide → 1-(piperidin-4-yl)-N-methyl-1H-indole-6-carboxamide

https://huagongshe.com/reaction/494915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-1-(1-benzyloxycarbonylpiperidin-4-yl)-1H-indole-6-carboxamideHCID 57682860—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product1-(piperidin-4-yl)-N-methyl-1H-indole-6-carboxamideHCID 5768283783.6%

Reaction Steps

1.77 g of N-methyl-1-(1-benzyloxycarbonylpiperidin-4-yl)-1H-indole-6-carboxamide was dissolved in 30 ml of methanol. Then, 200 mg of 10% palladium carbon was added to the obtained solution. The reaction atmosphere was replaced by hydrogen, and it was then stirred at room temperature. After completion of the reaction, 10% palladium carbon was filtered off from the reaction solution, and the reaction solution was then concentrated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate/methanol), followed by solidification from a mixed solution consisting of ethyl acetate, t-butylmethyl ether, and methanol, so as to obtain 973 mg of the subject compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538123B2
Source datasetuspto-grants-2009_05
ORD IDord-300aff1a8c3347148e59f89c6d1fa17c
Source noteuspto-grants-2009_05