Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369192Generated: October 27, 2026

HCID 23285064, compound → HCID 23285016, compound

https://huagongshe.com/reaction/369192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23285064HCID 23285064—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 23285016HCID 2328501685.8%

Reaction Steps

1.50 g of 7-chloro-3-methylthio-4-{4-[N-methyl-N-(2-phenylethyl)amino]-1-piperidinylcarbonyl}-oxindole was added to a suspension of 15 g of Raney nickel in 30 ml of methanol. The mixture was stirred at room temperature for 1 hour. The Raney nickel was separated by decantation and washed with methanol. The decanted solution and the washings were combined and concentrated under reduced pressure. The residue was purified by a silica gel column chromatography (eluant: methylene chloride/methanol=30/1). The product was converted into a hydrochloride in ethanol to obtain 0.63 g of 7-chloro-4-{4-[N-methyl-N-(2-phenylethyl)amino]-1-piperidinylcarbonyl}oxindole hydrochloride as a colorless amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136826
Source datasetuspto-grants-2000_10
ORD IDord-c599f5a08e894917920fd56287bf1f28
Source noteuspto-grants-2000_10