Technology Process of C22H23ClFN5O
There total 3 articles about C22H23ClFN5O which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
tris-(dibenzylideneacetone)dipalladium(0); potassium tert-butylate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene;
In
1,4-dioxane;
at 85 ℃;
Inert atmosphere;
DOI:10.1016/j.bmcl.2011.09.033
- Guidance literature:
-
Multi-step reaction with 3 steps
1: triethylamine / 0.5 h / 0 - 20 °C
2: N-ethyl-N,N-diisopropylamine / butan-1-ol
3: tris-(dibenzylideneacetone)dipalladium(0); potassium tert-butylate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 85 °C / Inert atmosphere
With
tris-(dibenzylideneacetone)dipalladium(0); potassium tert-butylate; triethylamine; N-ethyl-N,N-diisopropylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene;
In
1,4-dioxane; butan-1-ol;
3: Buchwald-Hartwig coupling;
DOI:10.1016/j.bmcl.2011.09.033
- Guidance literature:
-
Multi-step reaction with 2 steps
1: N-ethyl-N,N-diisopropylamine / butan-1-ol
2: tris-(dibenzylideneacetone)dipalladium(0); potassium tert-butylate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 85 °C / Inert atmosphere
With
tris-(dibenzylideneacetone)dipalladium(0); potassium tert-butylate; N-ethyl-N,N-diisopropylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene;
In
1,4-dioxane; butan-1-ol;
2: Buchwald-Hartwig coupling;
DOI:10.1016/j.bmcl.2011.09.033