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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109619Generated: October 31, 2026

1-(1-Methyl(4-piperidyl))-6-nitroindoline → 1-(1-Methyl-4-piperidyl)-indoline-6-ylamine

https://huagongshe.com/reaction/2109619

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Methyl(4-piperidyl))-6-nitroindolineHCID 18796623—
SolventMethanolHCID 887—
Product1-(1-Methyl-4-piperidyl)-indoline-6-ylamineHCID 21959560—

Reaction Steps

1-(1-Methyl(4-piperidyl))-6-nitroindoline (3 g, Step A) was dissolved in 100 mL MeOH and the mixture was bubbled with H2 for 10 min. 10% Pd/C (200 mg) was added and the mixture was stirred under H2 overnight. The mixture was filtered through Celite® and concentrated in vacuo to afford light yellow oil. MS: 232 (M+1). Calc'd. for C14H21N3−231.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514564B2
Source datasetuspto-grants-2009_04
ORD IDord-093071b1edb544558a66f7e27557b99f
Source noteuspto-grants-2009_04