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

HRID 605080Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 605080
[NH2:1][C:2]1[CH:3]=[C:4]([CH:16]=[CH:17][C:18]=1[S:19][C:20]1[CH:25]=[CH:24][C:23]([OH:26])=[CH:22][CH:21]=1)[C:5]([NH:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[Br:15])=[O:6].C([C:29]1[C:30]([N:36]=[CH:37][N:38]([CH3:40])C)=[N:31][C:32]([CH3:35])=[CH:33][CH:34]=1)#N.NC1C=C(C=CC=1SC1C=CC(O)=CC=1)C(NC1C=CC(Br)=CC=1)=O>>[Br:15][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[CH2:8][NH:7][C:5](=[O:6])[C:4]1[CH:16]=[CH:17][C:18]([S:19][C:20]2[CH:21]=[CH:22][C:23]([OH:26])=[CH:24][CH:25]=2)=[C:2]([NH:1][C:40]2[C:29]3[CH:34]=[CH:33][C:32]([CH3:35])=[N:31][C:30]=3[N:36]=[CH:37][N:38]=2)[CH:3]=1

Komponenten

4

Versuchsvorschrift

The product of Example 31A was reacted with the product of Example 9B using the procedure of Example 22C substituting the product of Example 31A 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 (60 mg, 71%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 2.68 (s, 3 H) 4.48 (d, J=5.52 Hz, 2 H) 6.84 (d, J=8.82 Hz, 2 H) 6.87-6.96 (m, 1 H) 7.16-7.25 (m, 1 H) 7.25-7.40 (m, 4 H) 7.56 (d, J=8.09 Hz, 1 H) 7.61 (d, J=8.82 Hz, 1 H) 7.76 (d, J=8.82 Hz, 1 H) 7.93 (s, 1 H) 8.58 (s, 1 H) 8.74-8.85 (m, 1 H) 8.94-9.21 (m, 1 H) 9.94 (s, 1 H) 10.16 (s, 1 H); MS (ESI+) m/z 572/574 (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-b31062c517d44c77b3d5044fda9c681f
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07910595B2

Notizen zur Reaktion

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