Ethanol → HCID 67259831, Verbindung

HRID 79259Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 79259
[CH2:1]([N:8]1[C:16]2[C:11](=[C:12]([N+:17]([O-])=O)[CH:13]=[CH:14][CH:15]=2)[C:10]([CH2:20][CH3:21])=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl-].[NH4+].C(O)C>[Fe].O>[CH2:1]([N:8]1[C:16]2[CH:15]=[CH:14][CH:13]=[C:12]([NH2:17])[C:11]=2[C:10]([CH2:20][CH3:21])=[N:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
85 °C

Versuchsvorschrift

A mixture of 1-benzyl-3-ethyl-4-nitro-1H-indazole (46.0 mg, 0.164 mmol), iron powder (91.3 mg, 1.64 mmol) and ammonium chloride (4.4 mg, 0.082 mmol) was stirred in a 4:1 mixture of ethanol and water (5 mL) with heating to 85° C. for 60 minutes. The solvent was removed under reduced pressure. Ethyl acetate (4 mL) and triethylamine (1 mL) was added and the mixture was heated for 15 minutes at 85° C. After cooling, the mixture was filtered through glass fiber filter paper, rinsing with methanol, dichloromethane and ethyl acetate. The filtrate was concentrated under reduced pressure to provide 1-benzyl-3-ethyl-1H-indazol-4-amine as an oil (40 mg).

Aufarbeitung

  1. customThe solvent was removed under reduced pressure
  2. additionEthyl acetate (4 mL) and triethylamine (1 mL) was added
  3. temperaturethe mixture was heated for 15 minutes at 85° C
  4. temperatureAfter cooling
  5. filtrationthe mixture was filtered through glass fiber
  6. filtrationfilter paper
  7. washrinsing with methanol, dichloromethane and ethyl acetate
  8. concentrationThe filtrate was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-e6fae5492da24fd1b1c3bbc42bdb3962
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08841455B2

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