Sodium Carbonate → 6-(1H-indol-4-yl)-1H-indazol-4-amine

HRID 42238

Reaktionsgleichung

Reaktionsgleichung von HRID 42238
Br[C:2]1[CH:3]=[C:4]([NH2:11])[C:5]2[CH:6]=[N:7][NH:8][C:9]=2[CH:10]=1.CC1(C)C(C)(C)OB([C:20]2[CH:28]=[CH:27][CH:26]=[C:25]3[C:21]=2[CH:22]=[CH:23][NH:24]3)O1.C(=O)([O-])[O-].[Na+].[Na+]>O1CCOCC1.O.ClCCl.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl>[NH:24]1[C:25]2[C:21](=[C:20]([C:2]3[CH:3]=[C:4]([NH2:11])[C:5]4[CH:6]=[N:7][NH:8][C:9]=4[CH:10]=3)[CH:28]=[CH:27][CH:26]=2)[CH:22]=[CH:23]1

Komponenten

8

Edukt 3

HCID 10340Sodium CarbonateHCID 113224711H-Indole-4-boronic acid, pinacol esterHCID 247280636-Bromo-1H-indazol-4-amine

Produkt 1

HCID 582680196-(1H-indol-4-yl)-1H-indazol-4-amineAusbeute 109,3 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 178418807HCID 178418807, VerbindungKatalysatorHCID 962WaterLösungsmittelHCID 6344DichloromethaneLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
115 °C

Versuchsvorschrift

6-Bromo-1H-indazol-4-amine (10 g, available from Sinova Inc.) and 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole (16.05 g, available from Frontier Scientific, Europe Ltd) were dissolved in 1,4-dioxane (60 ml) and water (60 ml). 2M sodium carbonate (70.7 ml) and Pd(dppf)Cl2-DCM adduct (1.93 g) were added and the mixture was heated at 115° C. for 18 hr. The reaction mixture was diluted with dichloromethane (200 ml) and the organic and aqueous layers were separated by hydrophobic frit. The aqueous layer was extracted with further quantities of dichloromethane (2×200 ml), using a hydrophobic frit to separate the layers. The organic layers were combined and silica (80 g) was added. The solvent was removed in vacuo to give a crude material that was purified by chromatography on silica gel (750 g cartridge, Flashmaster II) eluting with 0-100% ethyl acetate in cyclohexane over 60 minutes. The oil was dried in vacuo on a drying rack overnight. The resultant yellow foam was dissolved in dichloromethane (3×400 ml), removing the solvent in vacuo after each dissolution. Ethyl acetate (50 ml) was then added and the solvent was removed in vacuo. The solid obtained was dried in a vacuum oven to afford the title compound (12.8 g) as a yellow foam.

Aufarbeitung

  1. customthe organic and aqueous layers were separated by hydrophobic frit
  2. extractionThe aqueous layer was extracted with further quantities of dichloromethane (2×200 ml)
  3. customto separate the layers
  4. additionsilica (80 g) was added
  5. customThe solvent was removed in vacuo
  6. customto give a crude material that
  7. customwas purified by chromatography on silica gel (750 g cartridge, Flashmaster II)
  8. washeluting with 0-100% ethyl acetate in cyclohexane over 60 minutes
  9. customThe oil was dried in vacuo on a drying rack overnight
  10. dissolutionThe resultant yellow foam was dissolved in dichloromethane (3×400 ml)
  11. customremoving the solvent in vacuo
  12. dissolutionafter each dissolution
  13. additionEthyl acetate (50 ml) was then added
  14. customthe solvent was removed in vacuo
  15. customThe solid obtained
  16. customwas dried in a vacuum oven

Quellen und Nachweise

ORD-Eintrag
ord-3930262a914743309a99998ff69ffe44
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08536169B2

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