5-Methyl-2-phenylsulfanyl-phenylamine → 7-cyclopropyl-N-(5-methyl-2-phenylsulfanyl-phenyl)pyrido[2,3-d]pyrimidin-4-amine

HRID 607227Notes

Reaction equation

HRID 607227 reaction equation
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([S:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[C:6]([NH2:8])[CH:7]=1.C([C:18]1[C:19]([N:27]=[CH:28][N:29]([CH3:31])C)=[N:20][C:21]([CH:24]2[CH2:26][CH2:25]2)=[CH:22][CH:23]=1)#N.NC1C=C(C)C=CC=1SC1C=CC(O)=CC=1.C(C1C(N=CN(C)C)=NC(C)=CC=1)#N>>[CH:24]1([C:21]2[CH:22]=[CH:23][C:18]3[C:31]([NH:8][C:6]4[CH:7]=[C:2]([CH3:1])[CH:3]=[CH:4][C:5]=4[S:9][C:10]4[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=4)=[N:29][CH:28]=[N:27][C:19]=3[N:20]=2)[CH2:25][CH2:26]1

Participants

5

Procedure

The product from Example 5I was reacted with the product from Example 119A using the procedure from Example 102 substituting the product from Example 5I for the product from Example 6c and substituting the product from Example 119A for the product from Example 10B to provide the crude residue which was purified by trituration with methanol to provide the title compound. 1H NMR (300 MHz, DMSO-D6) δ ppm: 1.05-1.19 (m, 4H), 2.22-2.41 (m, 1H), 2.35 (s, 3H), 7.05-7.31 (m, 7H), 7.37 (s, 1H), 7.58 (d, J=8.46 Hz, 1H), 8.50 (s, 1H), 8.65 (d, J=8.46 Hz, 1H), 10.21 (s, 1H); MS (ESI)+ m/z 385 (M+H)+.

Workup

  1. customto provide the crude residue which
  2. customwas purified by trituration with methanol

Sources & evidence

ORD record
ord-757a14f4b7814fefb6976e59612990e9
Source dataset
uspto-grants-2011_03
Patent number
US07915411B2

Reaction notes

Loading…