(2R,3R)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid

Base Information

Chemical Name:(2R*,3R*)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid
CAS No.:107699-47-8
Molecular Formula:C₂₅H₃₇NO₅Si
Molecular Weight:459.658
Hs Code.:

Synonyms:(2R*,3R*)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid

Suppliers and Price of (2R*,3R*)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid

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 (2R*,3R*)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R*,3R*)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid

There total 5 articles about (2R*,3R*)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid 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: 85.0%

: 107699-46-7
benzyl (3R*,4R*,5R*)-5-(2'-tert-butyldimethylsilyloxyethyl)-3-p-methoxyphenyl-2-phenylisoxazolidine-4-carboxylate

: 107699-47-8
(2R*,3R*)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 2h; under 1520 Torr;

Reference yield:

: 102972-08-7
(3R*,3aR*,6S*,7aR*)-6-acetoxymethyl-3-p-methoxyphenyl-4-oxo-2-phenyl-tetrahydropyrano-<3,4-d>-isoxazolidine

: 107699-47-8
(2R*,3R*)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) aq. KOH, 2.) 18-crown-6 / 1.) dioxane, RT, overnight, 2.) DMF,

2: 85 percent / NaIO₄ / H₂O / 48 h / Ambient temperature

3: NaBH₃CN, aq. HCl / methanol / 1 h

4: imidazole / dimethylformamide / Ambient temperature

5: 85 percent / H₂ / 10percent Pd/C / aq. ethanol / 2 h / 1520 Torr

With 1H-imidazole; hydrogenchloride; potassium hydroxide; sodium periodate; 18-crown-6 ether; hydrogen; sodium cyanoborohydride; palladium on activated charcoal; In methanol; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 107699-44-5
benzyl (3R*,4R*,5R*)-5-(2'-oxoethyl)-3-p-methoxyphenyl-2-phenylisoxazolidine-4-carboxylate

: 107699-47-8
(2R*,3R*)-3-hydroxy-5-tert-butyldimethylsilyloxy-2-(R*-p-methoxyphenyl-N-phentlaminomethyl)-pentanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: NaBH₃CN, aq. HCl / methanol / 1 h

2: imidazole / dimethylformamide / Ambient temperature

3: 85 percent / H₂ / 10percent Pd/C / aq. ethanol / 2 h / 1520 Torr

With 1H-imidazole; hydrogenchloride; hydrogen; sodium cyanoborohydride; palladium on activated charcoal; In methanol; ethanol; N,N-dimethyl-formamide;