1-Methyl-3-aminopyrazole → HCID 11717721, compound
Reaction equation
[SH:1][C:2]1[NH:6][C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[N:3]=1.[NH2:11][C:12]1[CH:16]=[CH:15][N:14]([CH3:17])[N:13]=1.Cl[C:19]1[C:20]2[N:28]=[C:27](Cl)[CH:26]=[CH:25][C:21]=2[N:22]=[CH:23][N:24]=1>>[NH:3]1[C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=[C:2]1[S:1][C:27]1[CH:26]=[CH:25][C:21]2[N:22]=[CH:23][N:24]=[C:19]([NH:11][C:12]3[CH:16]=[CH:15][N:14]([CH3:17])[N:13]=3)[C:20]=2[N:28]=1Participants
4
Procedure
The compound of Example 62 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 2-mercapto-1H-benzimidazole, 3-amino-1-methyl-1H-pyrazole and 4,6-dichloro-pyrido[3,2-d]pyrimidine.
Sources & evidence
- ORD record
- ord-adde323467df43da81eb9c27f8b333de
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687502B2
Reaction notes
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