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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247263Generated: October 29, 2026

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

https://huagongshe.com/reaction/2247263

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 N2 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 a light yellow oil. MS:232 (M+1). Calc'd. for C14H21N3—231.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687643B2
Source datasetuspto-grants-2010_03
ORD IDord-b0b0286a35cc465c84b7112f828d1d32
Source noteuspto-grants-2010_03