3-Amino-5-methyl-4H-1,2,4-triazole → HCID 86703039, compound
Reaction equation
[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[C:7]([C:15]3[CH:22]=[CH:21][C:18]([CH:19]=[O:20])=[CH:17][CH:16]=3)=[N:8][C:9]3[N:10]([N:12]=[CH:13][CH:14]=3)[CH:11]=2)=[CH:2]1.CC1NN=C(N)[N:25]=1>>[CH3:14][C:13]1[N:25]=[C:9]2[N:8]=[C:7]([C:15]3[CH:22]=[CH:21][C:18]([CH:19]=[O:20])=[CH:17][CH:16]=3)[C:6]([C:3]3[CH:4]=[CH:5][S:1][CH:2]=3)=[CH:11][N:10]2[N:12]=1Participants
3
Procedure
This compound was prepared in a manner according to 4-(6-thiophen-3-yl-pyrazolo[1,5-a]pyrimidin-5-yl)-benzaldehyde by using 5-methyl-1,2,4-triazol-3-amine in the first step.
Workup
- customThis compound was prepared in a manner
Sources & evidence
- ORD record
- ord-64b89b59133044a293f5faee530f73b1
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957064B2
Reaction notes
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