Technology Process of (6-phenoxy-1,2,3,4-tetrahydronaphthalen-2-yl)(5-(pyridin-2-yl)-1,3,4-oxadiazol-2-yl)methanone
There total 18 articles about (6-phenoxy-1,2,3,4-tetrahydronaphthalen-2-yl)(5-(pyridin-2-yl)-1,3,4-oxadiazol-2-yl)methanone which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
Dess-Martin periodane;
In
dichloromethane;
at 20 ℃;
for 2h;
DOI:10.1021/jm101597x
- Guidance literature:
-
Multi-step reaction with 11 steps
1.1: copper diacetate / dichloromethane / 0.25 h / 20 °C / Molecular sieve
1.2: 17 h / 20 °C / Inert atmosphere
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C
3.1: Dess-Martin periodane / dichloromethane / 2 h / 20 °C
4.1: tetrahydrofuran; water / 16 h / 20 °C
5.1: hydrogenchloride / ethyl acetate / 16 h / Reflux; Inert atmosphere
6.1: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 20 °C
7.1: water; lithium hydroxide / tetrahydrofuran; methanol / 16 h / 20 °C
8.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 16 h / 20 °C
9.1: triethylamine; p-toluenesulfonyl chloride / dichloromethane / 16 h / 20 °C
10.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere
11.1: Dess-Martin periodane / dichloromethane / 2 h / 20 °C
With
1H-imidazole; hydrogenchloride; lithium aluminium tetrahydride; tetrabutyl ammonium fluoride; water; copper diacetate; Dess-Martin periodane; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; p-toluenesulfonyl chloride; lithium hydroxide;
In
tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm101597x