Ammonium Chloride → HCID 69652717, Verbindung

HRID 1790144Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1790144
[CH3:1][O:2][CH:3]([O:17][CH3:18])[CH2:4][N:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([N+:14]([O-])=O)[CH:12]=2)[CH2:7][NH:6]1.[NH4+].[Cl-]>C(O)C.O.[Fe]>[CH3:18][O:17][CH:3]([O:2][CH3:1])[CH2:4][N:5]1[C:13]2[C:8](=[CH:9][CH:10]=[C:11]([NH2:14])[CH:12]=2)[CH2:7][NH:6]1

Komponenten

5

Versuchsvorschrift

To a mixture of 1-(2,2-dimethoxyethyl)-6-nitro-2H-indazole (1.89 g, 7.52 mmol) and NH4Cl (337 mg, 6.01 mmol) in ethanol/H2O (2:1, 75 mL) at room temperature was added Fe (1.28 g, 23.7 mmol) and the mixture was heated for 2 hours at 70 C. The mixture was cooled to room temperature, filtered through celite, which was washed with hot methanol (5×20 mL), and the combined filtrate concentrated under reduced pressure. The residue was diluted with ethyl acetate (50 mL), filtered, the filtrate was concentrated under reduced pressure to provide 1-(2,2-dimethoxyethyl)-2H-indazol-6-ylamine as an amber oil. 1H NMR (300 MHz, DMSO-d6) δ ppm 3.26 (m, 6 H), 4.23 (d, J=5.42 Hz, 2 H), 4.71 (t, J=5.42 Hz, 1 H), 5.30 (s, 2 H), 6.49 (m, 2 H), 7.35 (m, 1 H), and 7.73 (s, 1 H); MS (ESI) 222 (M+H)+.

Aufarbeitung

  1. temperaturethe mixture was heated for 2 hours at 70 C
  2. filtrationfiltered through celite, which
  3. washwas washed with hot methanol (5×20 mL)
  4. concentrationthe combined filtrate concentrated under reduced pressure
  5. additionThe residue was diluted with ethyl acetate (50 mL)
  6. filtrationfiltered
  7. concentrationthe filtrate was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-818e4ca598ff4a3cb2d249174af30651
Quelldatensatz
uspto-grants-2006_07
Patentnummer
US07071182B2

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