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Odalasvir

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Odalasvir

Synonyms:Odalasvir

Suppliers and Price of Odalasvir
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The product has achieved commercial mass production*data from LookChem market partment
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Total 4 raw suppliers
Chemical Property of Odalasvir
Chemical Property:
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98%min *data from raw suppliers

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Technology Process of Odalasvir

There total 9 articles about Odalasvir 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:
C46H50N6*4CH4O3S; With triethylamine; In dichloromethane; at 10 ℃; for 0.5h; Industrial scale;
N-methoxycarbonyl-L-valine; With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; In dichloromethane; at 10 - 25 ℃; for 3.5h; Industrial scale;
DOI:10.1021/acs.oprd.1c00237
Guidance literature:
Multi-step reaction with 5 steps
1.1: acetic acid / ethyl acetate; tetrahydrofuran / 8 - 69 °C / Industrial scale
2.1: potassium acetate; [2,6-bis(2,4,6-triisopropylphenyl)phenyl(dicyclohexylphosphine)](allyl-η3)palladium(II) chloride / Isopropyl acetate / 5 h / 90 °C / Industrial scale
3.1: palladium diacetate; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; tetrabutylammomium bromide; caesium carbonate / water; toluene / 17 h / 90 °C / Inert atmosphere; Industrial scale
4.1: dichloromethane / 11 h / 20 - 35 °C / Reflux; Industrial scale
5.1: triethylamine / dichloromethane / 0.5 h / 10 °C / Industrial scale
5.2: 3.5 h / 10 - 25 °C / Industrial scale
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; [2,6-bis(2,4,6-triisopropylphenyl)phenyl(dicyclohexylphosphine)](allyl-η3)palladium(II) chloride; tetrabutylammomium bromide; potassium acetate; palladium diacetate; caesium carbonate; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; Isopropyl acetate; water; ethyl acetate; toluene; 2.1: |Miyaura Borylation Reaction / 3.1: |Suzuki Coupling;
DOI:10.1021/acs.oprd.1c00237
Guidance literature:
Multi-step reaction with 7 steps
1.1: ethyl acetate / Industrial scale
2.1: ethyl acetate; tetrahydrofuran / 2 h / 20 °C / Industrial scale
3.1: acetic acid / ethyl acetate; tetrahydrofuran / 8 - 69 °C / Industrial scale
4.1: potassium acetate; [2,6-bis(2,4,6-triisopropylphenyl)phenyl(dicyclohexylphosphine)](allyl-η3)palladium(II) chloride / Isopropyl acetate / 5 h / 90 °C / Industrial scale
5.1: palladium diacetate; dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; tetrabutylammomium bromide; caesium carbonate / water; toluene / 17 h / 90 °C / Inert atmosphere; Industrial scale
6.1: dichloromethane / 11 h / 20 - 35 °C / Reflux; Industrial scale
7.1: triethylamine / dichloromethane / 0.5 h / 10 °C / Industrial scale
7.2: 3.5 h / 10 - 25 °C / Industrial scale
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; [2,6-bis(2,4,6-triisopropylphenyl)phenyl(dicyclohexylphosphine)](allyl-η3)palladium(II) chloride; tetrabutylammomium bromide; potassium acetate; palladium diacetate; caesium carbonate; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; Isopropyl acetate; water; ethyl acetate; toluene; 4.1: |Miyaura Borylation Reaction / 5.1: |Suzuki Coupling;
DOI:10.1021/acs.oprd.1c00237
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