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2,3-Dihydro-1H-indole-2-carboxamide → 2-Aminomethylindoline

HRID 1601076
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1601076
[H-].[H-].[H-].[H-].[Li+].[Al+3].[NH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:9][CH:8]1[C:16]([NH2:18])=O>C1COCC1>[NH2:18][CH2:16][CH:8]1[CH2:9][C:10]2[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=2)[NH:7]1
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Komponenten

4

Edukt 2

HCID 139378102,3-Dihydro-1H-indole-2-carboxamideHCID 21226445Aluminium lithium hydride2×

Produkt 1

HCID 218304062-AminomethylindolineAusbeute 51 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

LAH (20 mL, 1M solution in THF) was added dropwise through a syringe to a solution of (±)-indoline-2-carboxamide (2.2 g, 13.6 mmol) in anhydrous THF (20 mL) with cooling, and the resulting solution was refluxed under argon for 5 h. More LAH (20 mL) was added, and reflux was continued for another 6 h. 10% aqueous THF was added dropwise with cooling to destroy excess LAH, and then Et2O was added. After stirring for 10 min, the colorless precipitate was removed by filtration and washed with THF. The filtrate was dried (K2CO3), concentrated, and purified by silica gel flash chromatography (90:10:0.2 CH2Cl2 /MeOH/Et3N). The title compound (1.02 g, 51%) was obtained as an amber oil: MS (ES) m/e 149.0 (M+H)+.

Aufarbeitung

  1. temperaturewith cooling
  2. temperaturethe resulting solution was refluxed under argon for 5 h
  3. temperaturereflux
  4. temperaturewith cooling
  5. customto destroy excess LAH
  6. additionEt2O was added
  7. customthe colorless precipitate was removed by filtration
  8. washwashed with THF
  9. dry with materialThe filtrate was dried (K2CO3)
  10. concentrationconcentrated
  11. custompurified by silica gel flash chromatography (90:10:0.2 CH2Cl2 /MeOH/Et3N)

Quellen und Nachweise

ORD-Eintrag
ord-1f0214d779e84795af0f569e1d3eee14
Quelldatensatz
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05977101

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