3-Pyridineacetonitrile → 6-Pyridin-3-yl-pyrido[2,3-d]pyrimidine-2,7-diamine
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]#[N:9])[CH:2]=1.[NH2:10][C:11]1[N:16]=[C:15]([NH2:17])[C:14]([CH:18]=O)=[CH:13][N:12]=1>>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[C:8]([NH2:9])=[N:17][C:15]3[N:16]=[C:11]([NH2:10])[N:12]=[CH:13][C:14]=3[CH:18]=2)[CH:2]=1Participants
3
Procedure
The procedure of Example 1 was followed to react 3-pyridylacetonitrile and 2,4-diamino-5-pyrimidine-carboxaldehyde to afford the title compound; mp 317-319° C. (dec).
Sources & evidence
- ORD record
- ord-9a9e5a7f91af4c9a86ea3e0dae85e5a1
- Source dataset
- uspto-grants-1999_09
- Patent number
- US05952342
Reaction notes
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