Technology Process of N9-benzylpyrido[3,4-b]indol-1(2H)-one
There total 4 articles about N9-benzylpyrido[3,4-b]indol-1(2H)-one which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 3 steps
1: sodium hydroxide / methanol; water / 5 h / 20 °C
2: diphenylphosphoranyl azide; triethylamine / 1,2-dichloro-benzene / 0.25 h / 60 °C / Inert atmosphere
3: 1,2-dichloro-benzene / 1 h / 180 °C / Microwave irradiation; Inert atmosphere
With
diphenylphosphoranyl azide; triethylamine; sodium hydroxide;
In
methanol; water; 1,2-dichloro-benzene;
2: |Curtius Rearrangement;
DOI:10.3987/COM-16-S(S)13
- Guidance literature:
-
Multi-step reaction with 4 steps
1: tetrahydrofuran / 12 h / 80 °C / Inert atmosphere
2: sodium hydroxide / methanol; water / 5 h / 20 °C
3: diphenylphosphoranyl azide; triethylamine / 1,2-dichloro-benzene / 0.25 h / 60 °C / Inert atmosphere
4: 1,2-dichloro-benzene / 1 h / 180 °C / Microwave irradiation; Inert atmosphere
With
diphenylphosphoranyl azide; triethylamine; sodium hydroxide;
In
tetrahydrofuran; methanol; water; 1,2-dichloro-benzene;
1: |Wittig Olefination / 3: |Curtius Rearrangement;
DOI:10.3987/COM-16-S(S)13
- Guidance literature:
-
Multi-step reaction with 2 steps
1: diphenylphosphoranyl azide; triethylamine / 1,2-dichloro-benzene / 0.25 h / 60 °C / Inert atmosphere
2: 1,2-dichloro-benzene / 1 h / 180 °C / Microwave irradiation; Inert atmosphere
With
diphenylphosphoranyl azide; triethylamine;
In
1,2-dichloro-benzene;
1: |Curtius Rearrangement;
DOI:10.3987/COM-16-S(S)13