Pyrazole → HCID 69104038, Verbindung

HRID 2217262Notizen

Reaktionsgleichung

[NH:1]1[CH:5]=[CH:4][CH:3]=[N:2]1.[H-].[Na+].[NH2:8][C:9]1[N:10]=[C:11]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:12]([C:16]2[CH:17]=[CH:18][C:19](=[O:25])[N:20]([CH:22]([CH3:24])[CH3:23])[CH:21]=2)=[N:13][C:14]=1Br.CCOC(C)=O>CN1C(=O)CCC1.O>[NH2:8][C:9]1[N:10]=[C:11]([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[C:12]([C:16]2[CH:17]=[CH:18][C:19](=[O:25])[N:20]([CH:22]([CH3:24])[CH3:23])[CH:21]=2)=[N:13][C:14]=1[N:1]1[CH:5]=[CH:4][CH:3]=[N:2]1

Komponenten

Reaktionsbedingungen

Temperatur: 100 °C

Versuchsvorschrift

To a solution of pyrazole (106 mg) in NMP (1.0 ml), was added 60% NaH (52 mg) under ice-bath cooling. After 5 minutes stirring, 5-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-1-isopropyl-2(1H)-pyridone (100 mg) was added to the mixture. And then the mixture was heated at 100° C. with stirring for 2 hours. After cooling, EtOAc and water were poured into the mixture, and the organic layer was separated, washed with water and brine, and dried over MgSO4. The solvent was removed under reduced pressure, and the residue was recrystallized from MeOH and dried in vacuo to give 5-[5-amino-3-phenyl-6-(1H-pyrazol-1-yl)-2-pyrazinyl]-1-isopropyl-2(1H)-pyridone (60 mg).

Aufarbeitung

temperaturecooling
stirringwith stirring for 2 hours
temperatureAfter cooling
customthe organic layer was separated
washwashed with water and brine
dry with materialdried over MgSO4
customThe solvent was removed under reduced pressure
customthe residue was recrystallized from MeOH
customdried in vacuo

Quellen und Nachweise

ORD-Eintrag: ord-02a904348a3a4c00b08734c7a9e620a1
Quelldatensatz: uspto-grants-2008_08
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07407961B2

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