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

HRID 2247263Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2247263
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[C:14]([N+:17]([O-])=O)[CH:15]=3)[CH2:10][CH2:9]2)[CH2:4][CH2:3]1>CO>[CH3:1][N:2]1[CH2:3][CH2:4][CH:5]([N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[C:14]([NH2:17])[CH:15]=3)[CH2:10][CH2:9]2)[CH2:6][CH2:7]1

Komponenten

3

Edukt 1

HCID 187966231-(1-Methyl(4-piperidyl))-6-nitroindoline

Produkt 1

HCID 219595601-(1-Methyl-4-piperidyl)-indoline-6-ylamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  1. customthe mixture was bubbled with N2 for 10 min
  2. addition10% Pd/C (200 mg) was added
  3. filtrationThe mixture was filtered through Celite®
  4. concentrationconcentrated in vacuo
  5. customto afford a light yellow oil

Quellen und Nachweise

ORD-Eintrag
ord-b0b0286a35cc465c84b7112f828d1d32
Quelldatensatz
uspto-grants-2010_03
Patentnummer
US07687643B2

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