Isopropanol → HCID 178503490, Verbindung

HRID 499092

Reaktionsgleichung

Reaktionsgleichung von HRID 499092
Cl[C:2]1[N:7]=[C:6]([S:8][CH3:9])[N:5]=[C:4]([NH:10][C:11]2[NH:15][N:14]=[C:13]([CH3:16])[CH:12]=2)[CH:3]=1.Cl.[CH:18]1([C:21]2([F:25])[CH2:24][NH:23][CH2:22]2)[CH2:20][CH2:19]1.C(N(C(C)C)CC)(C)C.C(O)(C)C>CCCCCC>[CH:18]1([C:21]2([F:25])[CH2:24][N:23]([C:2]3[N:7]=[C:6]([S:8][CH3:9])[N:5]=[C:4]([NH:10][C:11]4[NH:15][N:14]=[C:13]([CH3:16])[CH:12]=4)[CH:3]=3)[CH2:22]2)[CH2:20][CH2:19]1

Komponenten

6

Edukt 4

HCID 3776IsopropanolHCID 81531DiisopropylethylamineHCID 665896423-Cyclopropyl-3-fluoroazetidine hydrochlorideHCID 178418729HCID 178418729, Verbindung

Produkt 1

HCID 178503490HCID 178503490, VerbindungAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8058HexaneLösungsmittel

Reaktionsbedingungen

Temperatur
85 °C

Versuchsvorschrift

To a mixture of 6-chloro-N-(3-methyl-1H-pyrazol-5-yl)-2-(methylthio)pyrimidin-4-amine (150 g, 0.58 mol) and 3-cyclopropyl-3-fluoroazetidine hydrochloride (132.2 g, 0.87 mol) was added diisopropylethylamine (208 g, 1.61 mol) and isopropanol (1.125 L). The mixture was heated to reflux for 23 hours. The reaction was then cooled to 85° C. (a slightly hazy solution) and filtered. The homogeneous solution was concentrated to a minimal volume. EtOAc was then added (1 L) and the solution was concentrated to a minimal volume. EtOAc (1 L) and H2O (1 L) were then added and the layers were separated. Crystallized product began to crystallize out of the organic layer during the extraction. The aqueous layer was further extracted with EtOAc (500 ml). The 1st organic layer was concentrated to dryness to give a white solid. Hexane (750 ml) was added to the second organic extract and the slurry was stirred at ambient temperature, and then cooled to 0° C. for 30 min. The slurry was filtered and washed with copious Heptane. The filter cake was dried under vacuum. The filter cake and the white solid from the 1st extraction were combined to afford 155.1 g of the desired product. (155.1 g, 77%). 1H NMR (DMSO, 400 MHz) 0.44 (2H, m), 0.60 (2H, m), 1.38-1.43 (1H, m), 2.18 (3H, s), 2.42 (3H, s), 3.89-3.97 (4H, m), 5.92 (1H, br s), 6.04 (1H, br s), 9.23 (1H, s), 11.86 (1H, s). ES+ 335

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 23 hours
  3. filtrationfiltered
  4. concentrationThe homogeneous solution was concentrated to a minimal volume
  5. additionEtOAc was then added (1 L)
  6. concentrationthe solution was concentrated to a minimal volume
  7. additionEtOAc (1 L) and H2O (1 L) were then added
  8. customthe layers were separated
  9. customto crystallize out of the organic layer during the extraction
  10. extractionThe aqueous layer was further extracted with EtOAc (500 ml)
  11. concentrationThe 1st organic layer was concentrated to dryness
  12. customto give a white solid
  13. extractionorganic extract
  14. temperaturecooled to 0° C. for 30 min
  15. filtrationThe slurry was filtered
  16. washwashed with copious Heptane
  17. customThe filter cake was dried under vacuum
  18. extractionThe filter cake and the white solid from the 1st extraction

Quellen und Nachweise

ORD-Eintrag
ord-60e1b59e6e7b4f419745acb8cea65457
Quelldatensatz
uspto-grants-2010_08
Patentnummer
US07767672B2

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