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(3R,4S,5S)-3-amino-5-(4-amino-3-fluoro-5-((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)benzyl)-4-hydroxytetrahydro-2H-thiopyran 1,1-dioxide

Base Information Edit
  • Chemical Name:(3R,4S,5S)-3-amino-5-(4-amino-3-fluoro-5-((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)benzyl)-4-hydroxytetrahydro-2H-thiopyran 1,1-dioxide
  • CAS No.:1367877-85-7
  • Molecular Formula:C15H17F7N2O4S
  • Molecular Weight:454.366
  • Hs Code.:
  • Mol file:1367877-85-7.mol
(3R,4S,5S)-3-amino-5-(4-amino-3-fluoro-5-((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)benzyl)-4-hydroxytetrahydro-2H-thiopyran 1,1-dioxide

Synonyms:(3R,4S,5S)-3-amino-5-(4-amino-3-fluoro-5-((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)benzyl)-4-hydroxytetrahydro-2H-thiopyran 1,1-dioxide

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Chemical Property of (3R,4S,5S)-3-amino-5-(4-amino-3-fluoro-5-((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)benzyl)-4-hydroxytetrahydro-2H-thiopyran 1,1-dioxide Edit
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Technology Process of (3R,4S,5S)-3-amino-5-(4-amino-3-fluoro-5-((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)benzyl)-4-hydroxytetrahydro-2H-thiopyran 1,1-dioxide

There total 11 articles about (3R,4S,5S)-3-amino-5-(4-amino-3-fluoro-5-((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)benzyl)-4-hydroxytetrahydro-2H-thiopyran 1,1-dioxide 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:
Multi-step reaction with 2 steps
1: hydrogenchloride / tetrahydrofuran; 1,4-dioxane / 2 h / 25 °C / Inert atmosphere
2: palladium 10% on activated carbon; ammonia; hydrogen / methanol / 50 h / 25 °C / Inert atmosphere
With hydrogenchloride; palladium 10% on activated carbon; ammonia; hydrogen; In tetrahydrofuran; 1,4-dioxane; methanol;
DOI:10.1021/jm300069y
Guidance literature:
Multi-step reaction with 11 steps
1.1: thionyl chloride / 0 - 25 °C / Inert atmosphere
2.1: diisobutylaluminium hydride / tetrahydrofuran; hexane / 4 h / 0 - 5 °C / Inert atmosphere
2.2: 0.5 h / 25 °C / Cooling with ice; Inert atmosphere
3.1: phosphorus tribromide / 24 h / 25 °C / Inert atmosphere
4.1: potassium carbonate / acetone / 2.5 h / 25 - 30 °C / Inert atmosphere
5.1: palladium diacetate; triethylamine; triphenylphosphine / tert-butyl methyl ether / 16 h / 25 °C / Inert atmosphere
6.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / -70 °C / Inert atmosphere
7.1: Chiralpak AD-I / ethanol; n-heptane / Inert atmosphere
8.1: potassium hexamethylsilazane / tetrahydrofuran / 24 h / 25 °C / Inert atmosphere
9.1: potassium peroxymonosulfate / tetrahydrofuran; water / 2 h / 25 °C / Inert atmosphere
10.1: hydrogenchloride / tetrahydrofuran; 1,4-dioxane / 2 h / 25 °C / Inert atmosphere
11.1: palladium 10% on activated carbon; ammonia; hydrogen / methanol / 50 h / 25 °C / Inert atmosphere
With hydrogenchloride; lithium aluminium tetrahydride; thionyl chloride; potassium peroxymonosulfate; palladium 10% on activated carbon; ammonia; hydrogen; palladium diacetate; phosphorus tribromide; potassium hexamethylsilazane; diisobutylaluminium hydride; potassium carbonate; triethylamine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; hexane; n-heptane; tert-butyl methyl ether; water; acetone;
DOI:10.1021/jm300069y
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