Technology Process of methyl 4-oxo-6-(m-tolylethynyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxylate
There total 4 articles about methyl 4-oxo-6-(m-tolylethynyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxylate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
6-(m-tolylethynyl)-2,3-dihydro-1,8-naphthyridin-4(1H)-one;
With
lithium hexamethyldisilazane;
In
tetrahydrofuran;
at -75 ℃;
Inert atmosphere;
methyl chloroformate;
In
tetrahydrofuran;
at -75 - 0 ℃;
Inert atmosphere;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: toluene / 72 h / Reflux
2.1: trifluorormethanesulfonic acid / 3 h / 90 °C
3.1: triethylamine; tri-tert-butyl phosphine / N,N-dimethyl-formamide / 0.08 h / 20 °C / Inert atmosphere
3.2: 0.17 h / 20 °C / Inert atmosphere
3.3: 20 - 80 °C / Inert atmosphere
4.1: lithium hexamethyldisilazane / tetrahydrofuran / -75 °C / Inert atmosphere
4.2: -75 - 0 °C / Inert atmosphere
With
tri-tert-butyl phosphine; trifluorormethanesulfonic acid; triethylamine; lithium hexamethyldisilazane;
In
tetrahydrofuran; N,N-dimethyl-formamide; toluene;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: trifluorormethanesulfonic acid / 3 h / 90 °C
2.1: triethylamine; tri-tert-butyl phosphine / N,N-dimethyl-formamide / 0.08 h / 20 °C / Inert atmosphere
2.2: 0.17 h / 20 °C / Inert atmosphere
2.3: 20 - 80 °C / Inert atmosphere
3.1: lithium hexamethyldisilazane / tetrahydrofuran / -75 °C / Inert atmosphere
3.2: -75 - 0 °C / Inert atmosphere
With
tri-tert-butyl phosphine; trifluorormethanesulfonic acid; triethylamine; lithium hexamethyldisilazane;
In
tetrahydrofuran; N,N-dimethyl-formamide;