Benzylamine → HCID 118113935, compound
Reaction equation
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br:9][C:10]1[CH:11]=[CH:12][C:13]2[N:14]([CH:16]=[C:17]([C:19](OCC)=[O:20])[N:18]=2)[CH:15]=1>>[CH2:1]([NH:8][C:19]([C:17]1[N:18]=[C:13]2[CH:12]=[CH:11][C:10]([Br:9])=[CH:15][N:14]2[CH:16]=1)=[O:20])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
The title compound was prepared by essentially following the same procedures described for Intermediate I, using benzylamine and ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate as starting materials.
Sources & evidence
- ORD record
- ord-9862889ba9284a8c9ef056820211ee21
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09271969B2
Reaction notes
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