Benzenemethanamine, 3,4-dimethyl- → 2-Amino-4-(3,4-dimethyl-benylamino)-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.[CH3:19][C:20]1[CH:21]=[C:22]([CH:25]=[CH:26][C:27]=1[CH3:28])[CH2:23][NH2:24]>COCCOC>[NH2:1][C:2]1[N:7]=[C:6]([NH:24][CH2:23][C:22]2[CH:25]=[CH:26][C:27]([CH3:28])=[C:20]([CH3:19])[CH:21]=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 3,4-dimethylbenzylamine in DME. ES-MS m/e (%): 331 (M+H+, 100).
Sources & evidence
- ORD record
- ord-2df1c58841434891830eecd09f644b5c
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06586441B2
Reaction notes
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