3-tert-butyl-1-phenyl-1H-pyrazol-5-amine → HCID 44133720, Verbindung

HRID 217867

Reaktionsgleichung

Reaktionsgleichung von HRID 217867
C[Al](C)C.[C:5]([C:9]1[CH:13]=[C:12]([NH2:14])[N:11]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[N:10]=1)([CH3:8])([CH3:7])[CH3:6].[O:21]=[C:22]1[NH:27][C:26]2[N:28]=[CH:29][CH:30]=[C:31]([O:32][C:33]3[CH:34]=[C:35]([CH:40]=[CH:41][CH:42]=3)[C:36](OC)=[O:37])[C:25]=2[N:24]=[CH:23]1>C1COCC1>[C:5]([C:9]1[CH:13]=[C:12]([NH:14][C:36](=[O:37])[C:35]2[CH:40]=[CH:41][CH:42]=[C:33]([O:32][C:31]3[C:25]4[N:24]=[CH:23][C:22](=[O:21])[NH:27][C:26]=4[N:28]=[CH:29][CH:30]=3)[CH:34]=2)[N:11]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[N:10]=1)([CH3:8])([CH3:6])[CH3:7]

Komponenten

5

Edukt 3

HCID 7706343-tert-butyl-1-phenyl-1H-pyrazol-5-amineHCID 16682925TrimethylaluminumHCID 44134094HCID 44134094, Verbindung

Produkt 1

HCID 44133720HCID 44133720, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Method H1: A solution of AlMe3 (solution in toluene 2M, 0.85 mL, 1.68 mmol,) was added dropwise to a cooled (0 C) solution of 3-tert-butyl-1-phenyl-1H-pyrazol-5-amine (362 mg, 1.68 mmol) in THF (5.0 mL). When the addition was complete, the mixture was allowed to warm to room temperature and stirring was continued for 30 minutes. Then methyl 3-(3-oxo-3,4-dihydropyrido[2,3-b]pyrazin-8-yloxy)benzoate (100 mg, 0.336 mmol) was added and the mixture was heated under reflux for 19 h. The mixture was cooled to room temperature and carefully quenched with 5% aq HCl (3.0 mL). After evaporation of solvent, the residue was retaken in CH2Cl2, washed with saturated solution of NaHCO3 and dried over MgSO4 and evaporated under vacuum. The obtained residue was chromatographied (eluent: CH2Cl2/EtOAc: 2/1 towards 1/3) and the title compound was obtained as a slightly yellow solid (29 mg, 18%).

Aufarbeitung

  1. additionWhen the addition
  2. temperaturethe mixture was heated
  3. temperatureunder reflux for 19 h
  4. temperatureThe mixture was cooled to room temperature
  5. customcarefully quenched with 5% aq HCl (3.0 mL)
  6. customAfter evaporation of solvent
  7. washwashed with saturated solution of NaHCO3
  8. dry with materialdried over MgSO4
  9. customevaporated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-731975b3e712480689e05707bde82578
Quelldatensatz
uspto-grants-2012_06
Patentnummer
US08198279B2

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