N'-(3-Cyano-6-methyl-pyridin-2-yl)-N,N-dimethyl-formamidine → N-(3-Bromo-phenyl)-4-(4-hydroxy-phenylsulfanyl)-3-(7-methyl-pyrido[2,3-d]pyrimidin-4-ylamino)-benzamide

HRID 605075Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 605075
[NH2:1][C:2]1[CH:3]=[C:4]([CH:15]=[CH:16][C:17]=1[S:18][C:19]1[CH:24]=[CH:23][C:22]([OH:25])=[CH:21][CH:20]=1)[C:5]([NH:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([Br:14])[CH:9]=1)=[O:6].C([C:28]1[C:29]([N:35]=[CH:36][N:37]([CH3:39])C)=[N:30][C:31]([CH3:34])=[CH:32][CH:33]=1)#N.NC1C=C(C=CC=1SC1C=CC(O)=CC=1)C(NC1C=CC(Br)=CC=1)=O>>[Br:14][C:10]1[CH:9]=[C:8]([NH:7][C:5](=[O:6])[C:4]2[CH:15]=[CH:16][C:17]([S:18][C:19]3[CH:24]=[CH:23][C:22]([OH:25])=[CH:21][CH:20]=3)=[C:2]([NH:1][C:39]3[C:28]4[CH:33]=[CH:32][C:31]([CH3:34])=[N:30][C:29]=4[N:35]=[CH:36][N:37]=3)[CH:3]=2)[CH:13]=[CH:12][CH:11]=1

Komponenten

4

Versuchsvorschrift

The product of Example 26A was reacted with the product of Example 9B using the procedure of Example 22C substituting the product of Example 26A for the product of Example 22B and substituting the product of Example 9B for the product of Example 8E to provide the crude title compound which was purified by column chromatography on silica gel using methanol/dichloromethane as eluent to provide the title product (22 mg, 47%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 2.68 (s, 3 H) 6.81-6.89 (m, 2 H) 6.89-7.01 (m, 1 H) 7.22-7.38 (m, 4 H) 7.49-7.64 (m, 1 H) 7.67-7.89 (m, 2 H) 7.92-8.03 (m, 1 H) 8.04-8.17 (m, 1 H) 8.58 (s, 1 H) 8.70-8.91 (m, 1 H) 9.96 (s, 1 H) 10.20 (s, 1 H) 10.31 (s, 1 H); MS (ESI+) m/z 558/560 (M+H)+.

Aufarbeitung

  1. customto provide the crude title compound which
  2. customwas purified by column chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-7b1883574e2b45c3a5ab852ed3589fce
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07910595B2

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