Dimethylformamide → 4-[1-(4-amino-3-methyl-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl]-6-chloro-3-ethoxy-2-(3-methoxyazetidin-1-yl)benzonitrile

HRID 1499927Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1499927
C(=O)([O-])[O-].[Cs+].[Cs+].[CH3:7][C:8]1[C:16]2[C:11](=[N:12][CH:13]=[N:14][C:15]=2[NH2:17])[NH:10][N:9]=1.[Cl:18][C:19]1[C:24]([C:25]#[N:26])=[C:23]([N:27]2[CH2:30][CH:29]([O:31][CH3:32])[CH2:28]2)[C:22]([O:33][CH2:34][CH3:35])=[C:21]([CH:36](Cl)[CH3:37])[CH:20]=1.CN(C)C=O>CCOC(C)=O>[NH2:17][C:15]1[N:14]=[CH:13][N:12]=[C:11]2[N:10]([CH:36]([C:21]3[CH:20]=[C:19]([Cl:18])[C:24]([C:25]#[N:26])=[C:23]([N:27]4[CH2:30][CH:29]([O:31][CH3:32])[CH2:28]4)[C:22]=3[O:33][CH2:34][CH3:35])[CH3:37])[N:9]=[C:8]([CH3:7])[C:16]=12

Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 10796Cesium carbonateHCID 866778446-Chloro-4-(1-chloroethyl)-3-ethoxy-2-(3-methoxyazetidin-1-yl)benzonitrileHCID 178434474HCID 178434474, Verbindung

Produkt 1

HCID 715090894-[1-(4-amino-3-methyl-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl]-6-chloro-3-ethoxy-2-(3-methoxyazetidin-1-yl)benzonitrileAusbeute 20 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Cesium carbonate (50 mg, 0.2 mmol) was added to a mixture of 3-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (16 mg, 0.10 mmol) and 6-chloro-4-(1-chloroethyl)-3-ethoxy-2-(3-methoxyazetidin-1-yl)benzonitrile (30 mg, 0.09 mmol) in N,N-dimethylformamide (3 mL, 40 mmol) and the reaction was stirred at 80° C. overnight. The mixture was diluted with EtOAc, washed with water, brine, dried over Na2SO4, filtered and concentrated the crude product. The product was purified was purified by prep HPLC on a C-18 column eluting water:acetonitrile gradient buffered pH 10 to give the title compound as a white amorphous solid (0.007 g, 20%). The product was isolated as a racemic mixture. LCMS calculated for C21H25ClN7O2(M+H)+: m/z=442.1; found: 442.1. 1H NMR (400 MHz, DMSO-d6) δ 8.11 (s, 1H), 6.80 (s, 1H), 6.18 (d, J=7.1 Hz, 1H), 4.58-4.44 (m, 2H), 4.18 (m, 1H), 4.13-4.01 (m, 2H), 3.81-3.62 (m, 2H), 3.23 (s, 3H), 2.55 (s, 3H), 1.69 (d, J=7.1 Hz, 3H), 1.35 (t, J=7.0 Hz, 3H).

Aufarbeitung

  1. washwashed with water, brine
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated the crude product
  5. customThe product was purified
  6. customwas purified by prep HPLC on a C-18 column
  7. washeluting water

Quellen und Nachweise

ORD-Eintrag
ord-4fde2fc04fa74f73a7dfa6ccf5c1debd
Quelldatensatz
uspto-grants-2015_12
Patentnummer
US09199982B2

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