5-cyclopropyl-1H-1,2,4-triazol-3-amine → 4-(2-Cyclopropyl-6-phenyl-[1,2,4]triazolo[1,5-a]pyrimidin-5-yl)benzaldehyde
Reaction equation
[CH3:1][C:2]1[N:24]=[C:5]2[N:6]=[C:7]([C:16]3[CH:23]=[CH:22][C:19]([CH:20]=[O:21])=[CH:18][CH:17]=3)[C:8]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:9][N:4]2[N:3]=1.[CH:25]1(C2NN=C(N)N=2)C[CH2:26]1>>[CH:1]1([C:2]2[N:24]=[C:5]3[N:6]=[C:7]([C:16]4[CH:17]=[CH:18][C:19]([CH:20]=[O:21])=[CH:22][CH:23]=4)[C:8]([C:10]4[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=4)=[CH:9][N:4]3[N:3]=2)[CH2:26][CH2:25]1Participants
3
Procedure
This compound was prepared in a manner according to 4-(2-methyl-6-phenyl-[1,2,4]triazolo[1,5-a]pyrimidin-5-yl)-benzaldehyde by using 5-cyclopropyl-1,2,4-triazol-3-amine in the first step.
Workup
- customThis compound was prepared in a manner
Sources & evidence
- ORD record
- ord-9bbb1821f5d74d83abbf7d7b31f987dc
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957064B2
Reaction notes
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