5-Methylpyrazin-2-amine → HCID 178430626, compound
Reaction equation
[SH:1][C:2]1[N:6]=[CH:5][NH:4][N:3]=1.Cl[C:8]1[C:9]2[N:17]=[C:16](Cl)[CH:15]=[CH:14][C:10]=2[N:11]=[CH:12][N:13]=1.[NH2:19][C:20]1[CH:25]=[N:24][C:23]([CH3:26])=[CH:22][N:21]=1>>[CH3:26][C:23]1[N:24]=[CH:25][C:20]([NH:19][C:8]2[C:9]3[N:17]=[C:16]([S:1][C:2]4[N:6]=[CH:5][NH:4][N:3]=4)[CH:15]=[CH:14][C:10]=3[N:11]=[CH:12][N:13]=2)=[N:21][CH:22]=1Participants
4
Procedure
The compound of Example 42 was manufactured by the same method as in Example 31, by a similar method thereto or by a combination of such a method with a conventional method using 3-mercapto-[1,2,4]triazole, 4,6-dichloropyrido-[3,2-d]-pyrimidine and 2-amino-5-methylpyrazine.
Sources & evidence
- ORD record
- ord-f5aa5e1dc2264d2f8bbfb500e48d77c9
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687502B2
Reaction notes
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