Technology Process of 1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline
There total 6 articles about 1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
boron trifluoride diethyl etherate; trifluoroacetic anhydride;
In
benzene;
at 20 ℃;
for 1h;
DOI:10.1248/cpb.47.1269
- Guidance literature:
-
Multi-step reaction with 4 steps
1: NaI; Na2CO3; TEAB / dioxane / 144 h / Heating
2: Ac2O / 1 h / 60 °C
3: 96 percent / NaIO4 / methanol / 6 h / 20 °C
4: 84 percent / TFAA; BF3*Et2O / benzene / 1 h / 20 °C
With
sodium periodate; boron trifluoride diethyl etherate; tetraethylammonium bromide; acetic anhydride; sodium carbonate; trifluoroacetic anhydride; sodium iodide;
In
1,4-dioxane; methanol; benzene;
1: Condensation / 2: Formylation / 3: Oxidation / 4: Pummerer reaction;
DOI:10.1248/cpb.47.1269
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 83 percent / SOCl2 / pyridine / 10 h / 110 °C
2: NaI; Na2CO3; TEAB / dioxane / 144 h / Heating
3: Ac2O / 1 h / 60 °C
4: 96 percent / NaIO4 / methanol / 6 h / 20 °C
5: 84 percent / TFAA; BF3*Et2O / benzene / 1 h / 20 °C
With
sodium periodate; thionyl chloride; boron trifluoride diethyl etherate; tetraethylammonium bromide; acetic anhydride; sodium carbonate; trifluoroacetic anhydride; sodium iodide;
In
1,4-dioxane; pyridine; methanol; benzene;
1: Chlorination / 2: Condensation / 3: Formylation / 4: Oxidation / 5: Pummerer reaction;
DOI:10.1248/cpb.47.1269