1,2-Ethanediamine, N1-phenyl- → 2-Amino-4-(2-phenylamino-ethylamino)-6-pyridin-2-yl-pyrimidine-5-carbonitrile
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6](S(C)=O)[C:5]([C:11]#[N:12])=[C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=2)[N:3]=1.[C:19]1([NH:25][CH2:26][CH2:27][NH2:28])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>COCCOC>[NH2:1][C:2]1[N:7]=[C:6]([NH:28][CH2:27][CH2:26][NH:25][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:5]([C:11]#[N:12])=[C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=2)[N:3]=1Participants
4
Procedure
From 2-amino-4-methanesulfinyl-6-pyridin-2-yl-pyrimidine-5-carbonitrile and N-phenylethylenediamine in DME. ES-MS m/e (%): 332 (M+H+, 100).
Sources & evidence
- ORD record
- ord-502c6cc3522d4e1bac902e5e8101b7e4
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06586441B2
Reaction notes
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