Triethylamine → 4-[(3-Oxo-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]benzamide

HRID 225502

Reaktionsgleichung

Reaktionsgleichung von HRID 225502
[CH3:1]CCP(=O)=O.C[C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:15]2[N:20]=[C:19]([C:21]3[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=3)[CH:18]=[CH:17][N:16]=2)=[CH:10][C:9]=1[NH2:27].[O:28]=[C:29]1[NH:34][CH2:33][CH2:32][N:31]([CH2:35][C:36]2[CH:44]=[CH:43][C:39]([C:40](O)=[O:41])=[CH:38][CH:37]=2)[CH2:30]1.C(N(CC)CC)C.C(=O)([O-])O.[Na+]>CN(C)C=O>[O:28]=[C:29]1[NH:34][CH2:33][CH2:32][N:31]([CH2:35][C:36]2[CH:44]=[CH:43][C:39]([C:40]([NH:27][C:9]3[CH:8]=[CH:13][C:12]([CH3:1])=[C:11]([NH:14][C:15]4[N:20]=[C:19]([C:21]5[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=5)[CH:18]=[CH:17][N:16]=4)[CH:10]=3)=[O:41])=[CH:38][CH:37]=2)[CH2:30]1

Komponenten

7

Versuchsvorschrift

A solution of propylphosphonic anhydride in N,N-dimethylformamide (Fluka, Buchs, Switzerland; 1.3 mL of 50%, 2.25 mmol) is added dropwise to a stirred mixture of 4-methyl-N-[4-(3-pyridinyl)-2-pyrimidinyl]-1,3-benzenediamine (416 mg, 1.5 mmol), 4-[(3-oxo-1-piperazinyl)methyl]benzoic acid (351 mg, 1.5 mmol) and triethylamine (1.7 mL, 12 mmol) in dry N,N-dimethylformamide (4 mL). The mixture is stirred for 17 hours at room temperature and then treated with saturated aqueous sodium hydrogen carbonate solution (100 mL). The resulting precipitate is filtered, washed with water, dried and recrystallised from methanol to give the title compound as a cream crystalline solid.

Aufarbeitung

  1. filtrationThe resulting precipitate is filtered
  2. washwashed with water
  3. customdried
  4. customrecrystallised from methanol

Quellen und Nachweise

ORD-Eintrag
ord-c3e61f6688dc4d85bd0d7f3e4111673b
Quelldatensatz
uspto-grants-2009_07
Patentnummer
US07557105B2

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