Technology Process of Propanoic acid, 2,2-dimethyl-, 4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl ester
There total 12 articles about Propanoic acid, 2,2-dimethyl-, 4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yl ester which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
4-fluoro-2-methyl-1H-indol-5-ol;
With
1,4-diaza-bicyclo[2.2.2]octane;
In
acetonitrile;
at 20 - 29 ℃;
for 1.16667h;
Large scale;
4-chloro-5-methylpyrrolo[1,2-f ][1,2,4]triazin-6-yl pivalate;
In
acetonitrile;
at 26 - 28 ℃;
for 3h;
Large scale;
DOI:10.1021/op400242j
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: potassium tert-butylate / tetrahydrofuran / 7.75 h / 10 °C / Large scale
1.2: 5.5 h / 10 - 22 °C / Large scale
2.1: sulfuric acid / acetic acid / 6.42 h / 70 °C / Large scale
3.1: potassium carbonate / 18.83 h / 9 - 25 °C / Reflux; Large scale
4.1: aluminum (III) chloride; trimethylamine hydrochloride / dichloromethane / 6.75 h / 22 - 42 °C / 2250.23 Torr / Large scale
5.1: sodium dithionite / methanol; water / 5 h / 20 - 25 °C / Large scale
6.1: 1,4-diaza-bicyclo[2.2.2]octane / acetonitrile / 1.17 h / 20 - 29 °C / Large scale
6.2: 3 h / 26 - 28 °C / Large scale
With
1,4-diaza-bicyclo[2.2.2]octane; aluminum (III) chloride; sodium dithionite; sulfuric acid; potassium tert-butylate; trimethylamine hydrochloride; potassium carbonate;
In
tetrahydrofuran; methanol; dichloromethane; water; acetic acid; acetonitrile;
5.1: |Reissert Indole Synthesis;
DOI:10.1021/op400242j
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: trichlorophosphate / acetonitrile / 0.13 h / 23 - 24 °C / Large scale
1.2: 11.5 h / 22 - 85 °C / Large scale
2.1: 1,4-diaza-bicyclo[2.2.2]octane / acetonitrile / 1.17 h / 20 - 29 °C / Large scale
2.2: 3 h / 26 - 28 °C / Large scale
With
1,4-diaza-bicyclo[2.2.2]octane; trichlorophosphate;
In
acetonitrile;
DOI:10.1021/op400242j