Reaction equation
N1CCCC1.[Br:6][C:7]1[CH:8]=[CH:9][C:10]2[N:11]([N:13]=[C:14]([N:16]3[CH2:21][CH2:20]O[CH2:18][CH2:17]3)[N:15]=2)[CH:12]=1>>[Br:6][C:7]1[CH:8]=[CH:9][C:10]2[N:11]([N:13]=[C:14]([N:16]3[CH2:21][CH2:20][CH2:18][CH2:17]3)[N:15]=2)[CH:12]=1Participants
3
Procedure
Using pyrrolidine, this compound was prepared following the same method as for the synthesis of 6-bromo-2-morpholin-4-yl-[1,2,4]triazolo[1,5-a]pyridine Off white solid (1.0 g, 41%). MS: m/z=268 (M+H+).
Workup
- customthis compound was prepared
Sources & evidence
- ORD record
- ord-e12bd21b6088435b9a7edca7cbdda269
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09227970B2
Linked notes
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