5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-1-phenyl-1H-tetrazole

Base Information

Chemical Name:5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-1-phenyl-1H-tetrazole
CAS No.:1514894-29-1
Molecular Formula:C₃₂H₅₈N₄O₃SSi₂
Molecular Weight:635.075
Hs Code.:

Synonyms:5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-1-phenyl-1H-tetrazole

Suppliers and Price of 5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-1-phenyl-1H-tetrazole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-1-phenyl-1H-tetrazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-1-phenyl-1H-tetrazole

There total 9 articles about 5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-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:

Reference yield: 70.0%

: 1514894-28-0
(5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-ol

: 86-93-1
1-Phenyl-1H-tetrazole-5-thiol

: 1514894-29-1
5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-1-phenyl-1H-tetrazole

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20 ℃; for 3h;
DOI:10.1021/ol403246j

Reference yield:

: 50727-94-1,62777-72-4,62960-04-7,71030-55-2,76985-26-7,82188-73-6,112456-40-3,112456-65-2,62777-71-3
(2R,3R)-3-methyl-3-(4-methyl-3-pentenyl)oxiranemethanol

: 1514894-29-1
5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-1-phenyl-1H-tetrazole

Guidance literature:: Multi-step reaction with 8 steps

1.1: triethylamine / dichloromethane / 0.83 h / 0 °C

2.1: potassium carbonate; potassium hexacyanoferrate(III); C₄₈H₅₄N₆O₄; osmium(VIII) oxide; methanesulfonamide / water; tert-butyl alcohol / 24 h / 0 °C

2.2: CSA / 1 h / 0 °C

3.1: potassium carbonate / methanol / 1 h / 0 °C

4.1: 1H-imidazole; dmap / N,N-dimethyl-formamide / 2 h / 0 - 20 °C

5.1: copper(l) iodide / tetrahydrofuran / 2 h

6.1: 1H-imidazole / N,N-dimethyl-formamide / 1 h / 0 °C / Inert atmosphere

7.1: mercury(II) diacetate / tetrahydrofuran; water / 20 h / 20 °C

7.2: 1 h / 0 °C

7.3: 1.5 h

8.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 3 h / 0 - 20 °C

With 1H-imidazole; dmap; copper(l) iodide; osmium(VIII) oxide; methanesulfonamide; di-isopropyl azodicarboxylate; C₄₈H₅₄N₆O₄; mercury(II) diacetate; potassium carbonate; triethylamine; triphenylphosphine; potassium hexacyanoferrate(III); In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol; 2.1: |Sharpless Dihydroxylation / 8.1: |Mitsunobu Displacement;
DOI:10.1021/ol403246j

Reference yield:

: 61573-90-8,93221-71-7,93221-74-0,126874-40-6,126874-41-7
((2R,3R)-3-methyl-3-(4-methylpent-3-en-1-yl)oxiran-2-yl)methyl methanesulfonate

: 1514894-29-1
5-(((5R)-5-((2S,5S)-2-methyl-5-(2-((triethylsilyl)oxy)propan-2-yl)tetrahydrofuran-2-yl)-5-((triethylsilyl)oxy)pentan-2-yl)thio)-1-phenyl-1H-tetrazole

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate; potassium hexacyanoferrate(III); C₄₈H₅₄N₆O₄; osmium(VIII) oxide; methanesulfonamide / water; tert-butyl alcohol / 24 h / 0 °C

1.2: CSA / 1 h / 0 °C

2.1: potassium carbonate / methanol / 1 h / 0 °C

3.1: 1H-imidazole; dmap / N,N-dimethyl-formamide / 2 h / 0 - 20 °C

4.1: copper(l) iodide / tetrahydrofuran / 2 h

5.1: 1H-imidazole / N,N-dimethyl-formamide / 1 h / 0 °C / Inert atmosphere

6.1: mercury(II) diacetate / tetrahydrofuran; water / 20 h / 20 °C

6.2: 1 h / 0 °C

6.3: 1.5 h

7.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 3 h / 0 - 20 °C

With 1H-imidazole; dmap; copper(l) iodide; osmium(VIII) oxide; methanesulfonamide; di-isopropyl azodicarboxylate; C₄₈H₅₄N₆O₄; mercury(II) diacetate; potassium carbonate; triphenylphosphine; potassium hexacyanoferrate(III); In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; tert-butyl alcohol; 1.1: |Sharpless Dihydroxylation / 7.1: |Mitsunobu Displacement;
DOI:10.1021/ol403246j