2-Chloro-6-methylaniline → 4-[2-[(2-chloro-6-methylphenyl)amino]-4-pyridinyl]-N-(2-methoxy-1-methylethyl)-2-pyrimidinamine

HRID 913288Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 913288
Cl[C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][N:11]=[C:10]([NH:14][CH:15]([CH3:19])[CH2:16][O:17][CH3:18])[N:9]=2)[CH:5]=[CH:4][N:3]=1.[Cl:20][C:21]1[CH:27]=[CH:26][CH:25]=[C:24]([CH3:28])[C:22]=1[NH2:23].C(=O)([O-])[O-].[Cs+].[Cs+]>C1(C)C=CC=CC=1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[Cl:20][C:21]1[CH:27]=[CH:26][CH:25]=[C:24]([CH3:28])[C:22]=1[NH:23][C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][N:11]=[C:10]([NH:14][CH:15]([CH3:19])[CH2:16][O:17][CH3:18])[N:9]=2)[CH:5]=[CH:4][N:3]=1

Komponenten

6

Versuchsvorschrift

To a solution of 4-(2-chloro-4-pyridinyl)-N-(2-methoxy-1-methylethyl)-2-pyrimidinamine (i.e., the product of Step B) (100 mg, 0.35 mmol) in toluene (10 mL) was added 2-chloro-6-methylaniline (102 mg, 0.72 mmol), cesium carbonate (350 mg, 1.07 mmol), palladium(II) acetate (4 mg, 0.017 mmol) and ((±)-BINAP) (22 mg, 0.035 mmol), and the resulting mixture was stirred at reflux for 30 h. After cooling to room temperature, the mixture was concentrated, and purified using column chromatography on silica gel eluted with 40% ethyl acetate in hexanes to give 30 mg of the title compound as a solid.

Aufarbeitung

  1. temperatureat reflux for 30 h
  2. concentrationthe mixture was concentrated
  3. custompurified
  4. washeluted with 40% ethyl acetate in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-6897530edede4bc380f1d54a73e03c54
Quelldatensatz
uspto-grants-2011_09
Patentnummer
US08026359B2

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