tert-Butyl isocyanoacetate → Tert-butyl imidazo[1,5-a]quinoxaline-3-carboxylate
Reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=[CH:3][C:2]=1O.[N+:12]([CH2:14][C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])#[C-:13]>>[CH:13]1[N:1]2[C:10]3[C:5]([N:4]=[CH:3][C:2]2=[C:14]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[N:12]=1)=[CH:6][CH:7]=[CH:8][CH:9]=3Participants
3
Procedure
M.p. 187°-190° C., from 2-quinoxalinol and tert-butyl isocyanoacetate. (Compound 4)
Sources & evidence
- ORD record
- ord-661450db4b474366839fc454e2dfdecc
- Source dataset
- uspto-grants-1991_07
- Patent number
- US05034530
Reaction notes
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