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C20H15F2N3O2S

Base Information
  • Chemical Name:C20H15F2N3O2S
  • CAS No.:1372148-89-4
  • Molecular Formula:C20H15F2N3O2S
  • Molecular Weight:399.421
  • Hs Code.:
C<sub>20</sub>H<sub>15</sub>F<sub>2</sub>N<sub>3</sub>O<sub>2</sub>S

Synonyms:C20H15F2N3O2S

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Chemical Property of C20H15F2N3O2S
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Technology Process of C20H15F2N3O2S

There total 4 articles about C20H15F2N3O2S which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; triethylamine; In 1,4-dioxane; for 5h; Reflux;
DOI:10.1055/s-0031-1290079
Guidance literature:
Multi-step reaction with 3 steps
1.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -40 °C / Inert atmosphere
1.2: 1.5 h / -40 - 20 °C
1.3: 0.33 h / 5 - 20 °C
2.1: potassium phosphate / dimethyl sulfoxide / 0.5 h / 100 °C
3.1: dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; triethylamine / 1,4-dioxane / 5 h / Reflux
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; palladium diacetate; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; 1,4-dioxane; dimethyl sulfoxide; 3.1: Suzuki-Miyaura coupling;
DOI:10.1055/s-0031-1290079
Guidance literature:
Multi-step reaction with 2 steps
1: potassium phosphate / dimethyl sulfoxide / 0.5 h / 100 °C
2: dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; triethylamine / 1,4-dioxane / 5 h / Reflux
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; palladium diacetate; triethylamine; In 1,4-dioxane; dimethyl sulfoxide; 2: Suzuki-Miyaura coupling;
DOI:10.1055/s-0031-1290079
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