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Dimethylformamide → HCID 68553177, Verbindung

HRID 2382100
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2382100
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][N:7]=[CH:8][CH:9]=2)[NH:4][CH:3]=1.CC([O-])(C)C.[K+].O(C(OC(C)(C)C)=O)C(OC(C)(C)C)=O.C[N:33](C=O)C>>[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][N:7]=[CH:8][CH:9]=2)[N:4]([NH2:33])[CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 6228DimethylformamideHCID 90495Di-tert-butyl dicarbonateHCID 213006013-Methyl-1H-pyrrolo[2,3-C]pyridineHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 68553177HCID 68553177, VerbindungAusbeute 35 %

Versuchsvorschrift

A mixture of 3-methyl-1H-pyrrolo[2,3-c]pyridine (1.21 g, 9.16 mmol), KOtBu (2.05 g, 18.3 mmol) in DMF (41 mL) is purged with N2 and stirred at rt for 2 h. Chloramine in ether (0.15 M, 92 mL) is added and the mixture is stirred for 20 min. The reaction is cooled to 00 C. and a solution of Na2S2O3 (5 g) in water (80 mL) is added. The mixture is stirred for 10 min, and then concentrated in vacuo. The residue is triturated in DCM and filtered. DCM is added, cooled to 0° C. and charged with BOC2O (541 mg, 2.48 mmol). The resulting mixture is separated by silica gel chromatography eluting with 10% MeOH in DCM to afford 3-methyl-pyrrolo[2,3-c]pyridin-1-yl amine (468 mg, 35%). MS: 148 (M+H); 1H NMR (300 MHz, CDCl3): δ 8.85 (s, 1H), 8.27 (d, 1H), 7.46 (d, 1H), 7.09 (s, 1H), 2.30 (s, 3H).

Aufarbeitung

  1. customis purged with N2
  2. additionChloramine in ether (0.15 M, 92 mL) is added
  3. stirringthe mixture is stirred for 20 min
  4. temperatureThe reaction is cooled to 00 C
  5. additionand a solution of Na2S2O3 (5 g) in water (80 mL) is added
  6. stirringThe mixture is stirred for 10 min
  7. concentrationconcentrated in vacuo
  8. customThe residue is triturated in DCM
  9. filtrationfiltered
  10. additionDCM is added
  11. temperaturecooled to 0° C.
  12. customThe resulting mixture is separated by silica gel chromatography
  13. washeluting with 10% MeOH in DCM

Quellen und Nachweise

ORD-Eintrag
ord-27f12b68a20c4697b651d13d02a9b3b0
Quelldatensatz
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08258130B2

Notizen zur Reaktion

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