Technology Process of C31H43N3O5SSi
There total 10 articles about C31H43N3O5SSi which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
pyridine;
In
dichloromethane;
for 0.333333h;
Cooling with ice;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: sodium hydroxide / water / 20 °C / Inert atmosphere
2.1: oxalyl dichloride / N,N-dimethyl-formamide; 1,4-dioxane / 20 °C / Inert atmosphere
2.2: 5 °C / Inert atmosphere
3.1: 1H-imidazole / N,N-dimethyl-formamide / 2 h / 12 °C / Inert atmosphere; Industrial scale
4.1: tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / toluene / 70 °C / Inert atmosphere
5.1: Wilkinson's catalyst / acetonitrile; water / 100 °C / Inert atmosphere
6.1: N,N-dimethyl-formamide; dichloromethane / 3 h / -3 - -1 °C / Inert atmosphere; Industrial scale
With
1H-imidazole; tris-(dibenzylideneacetone)dipalladium(0); Wilkinson's catalyst; oxalyl dichloride; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium hydroxide; sodium t-butanolate;
In
1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1021/acs.oprd.6b00415
- Guidance literature:
-
Multi-step reaction with 5 steps
1: palladium diacetate; triphenylphosphine; potassium phosphate / toluene; water / 20 h / 87 °C / Inert atmosphere; Industrial scale
2: sodium hydroxide / methanol; tetrahydrofuran; water / 2 h / 47 °C / Inert atmosphere; Industrial scale
3: hydrogenchloride / water; acetone / 50 °C / Inert atmosphere; Industrial scale
4: dmap; pyridine; trichlorophosphate / N,N-dimethyl-formamide; dichloromethane / 1 h / -4 - -3 °C / Inert atmosphere; Industrial scale
5: N,N-dimethyl-formamide; dichloromethane / 3 h / -3 - -1 °C / Inert atmosphere; Industrial scale
With
pyridine; hydrogenchloride; dmap; potassium phosphate; palladium diacetate; triphenylphosphine; sodium hydroxide; trichlorophosphate;
In
tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene;
1: |Suzuki Coupling;
DOI:10.1021/acs.oprd.6b00415