2,6-Dimethylaniline → HCID 118113930, compound
Reaction equation
[CH3:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:3]=1[NH2:4].[Br:10][C:11]1[CH:12]=[CH:13][C:14]2[N:15]([CH:17]=[C:18]([C:20](OCC)=[O:21])[N:19]=2)[CH:16]=1>>[Br:10][C:11]1[CH:12]=[CH:13][C:14]2[N:15]([CH:17]=[C:18]([C:20]([NH:4][C:3]3[C:5]([CH3:9])=[CH:6][CH:7]=[CH:8][C:2]=3[CH3:1])=[O:21])[N:19]=2)[CH:16]=1Participants
3
Procedure
The title compound was prepared by using procedures analogous to those described for the synthesis of Intermediate I, using 2,6-dimethylaniline and ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate as starting materials.
Sources & evidence
- ORD record
- ord-4f01d20ce1fc4c3f9573261e091a2e92
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09271969B2
Reaction notes
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