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5-((2S,5R,9S)-9-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)-2-methyldecylsulfonyl)-1-phenyl-1H-tetrazole

Base Information
  • Chemical Name:5-((2S,5R,9S)-9-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)-2-methyldecylsulfonyl)-1-phenyl-1H-tetrazole
  • CAS No.:1267597-38-5
  • Molecular Formula:C26H46N4O5SSi
  • Molecular Weight:554.827
  • Hs Code.:
5-((2S,5R,9S)-9-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)-2-methyldecylsulfonyl)-1-phenyl-1H-tetrazole

Synonyms:5-((2S,5R,9S)-9-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)-2-methyldecylsulfonyl)-1-phenyl-1H-tetrazole

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Chemical Property of 5-((2S,5R,9S)-9-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)-2-methyldecylsulfonyl)-1-phenyl-1H-tetrazole
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Technology Process of 5-((2S,5R,9S)-9-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)-2-methyldecylsulfonyl)-1-phenyl-1H-tetrazole

There total 12 articles about 5-((2S,5R,9S)-9-(tert-butyldimethylsilyloxy)-5-(methoxymethoxy)-2-methyldecylsulfonyl)-1-phenyl-1H-tetrazole 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 6 steps
1.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -90 °C / Inert atmosphere
1.2: -90 - 20 °C / Inert atmosphere
2.1: zinc trifluoromethanesulfonate; triethylamine; N-methyl ephedrine / toluene / 20 °C / Inert atmosphere
2.2: 20 °C / Inert atmosphere
3.1: tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
4.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 20 °C
5.1: triphenylphosphine; diethylazodicarboxylate / toluene / 20 °C / Inert atmosphere
6.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C / Inert atmosphere
With oxalyl dichloride; palladium 10% on activated carbon; hydrogen; tetra-(n-butyl)ammonium iodide; zinc trifluoromethanesulfonate; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; diethylazodicarboxylate; N-methyl ephedrine; In tetrahydrofuran; dichloromethane; toluene; 1.1: Swern oxidation / 1.2: Swern oxidation;
DOI:10.1002/chem.201001752
Guidance literature:
Multi-step reaction with 6 steps
1.1: potassium carbonate / methanol / 2 h / 20 °C / Inert atmosphere
2.1: zinc trifluoromethanesulfonate; triethylamine; N-methyl ephedrine / toluene / 20 °C / Inert atmosphere
2.2: 20 °C / Inert atmosphere
3.1: tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
4.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 20 °C
5.1: triphenylphosphine; diethylazodicarboxylate / toluene / 20 °C / Inert atmosphere
6.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C / Inert atmosphere
With palladium 10% on activated carbon; hydrogen; tetra-(n-butyl)ammonium iodide; zinc trifluoromethanesulfonate; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; diethylazodicarboxylate; N-methyl ephedrine; In tetrahydrofuran; methanol; dichloromethane; toluene;
DOI:10.1002/chem.201001752
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