(2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol

Base Information

Chemical Name:(2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol
CAS No.:855594-63-7
Molecular Formula:C₃₇H₅₇N₂O₉P
Molecular Weight:704.841
Hs Code.:

Synonyms:(2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol

Suppliers and Price of (2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol

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 (2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol

There total 11 articles about (2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol 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%

: 855526-99-7
(2S,3R)-1-O-[(2'-azidoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol

: 855594-63-7
(2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol

Guidance literature:: With 1.3-propanedithiol; triethylamine; In methanol; at 20 ℃;
DOI:10.1021/jo050513u

Reference yield:

: dodec-11-en-1-ynyl-trimethyl-silane

: 855594-63-7
(2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol

Guidance literature:: Multi-step reaction with 9 steps

1.1: 0.67 g / NaOH / diethyl ether; H₂O / 1 h / 20 °C

2.1: n-BuLi / tetrahydrofuran; hexane / 2 h / -78 °C

2.2: 76 percent / HMPA / tetrahydrofuran; hexane / 2.5 h / -78 °C

3.1: 58 percent / Red-Al / diethyl ether; toluene / 4.17 h / 0 - 20 °C

4.1: 92 percent / iPr₂NEt / CH₂Cl₂ / 0 - 20 °C

5.1: 9-BBN-H / tetrahydrofuran / 20 °C

5.2: 73 percent / Pd(PPh₃)4; K₃PO₄ / tetrahydrofuran; dioxane; H₂O / 85 °C

6.1: 88 percent / acetic acid / H₂O / 5 h / 80 °C

7.1: pyridine / diethyl ether / Heating

8.1: 206 mg / H₂O / diethyl ether / 20 °C

9.1: 85 percent / Et₃N; 1,3-propanedithiol / methanol / 20 °C

With pyridine; 1.3-propanedithiol; sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; n-butyllithium; water; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; water; toluene; 5.2: Suzuki coupling;
DOI:10.1021/jo050513u

Reference yield:

: 855526-95-3
(S)-4-((E)-(R)-1-Hydroxy-trideca-2,12-dienyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

: 855594-63-7
(2S,3R)-1-O-[(2'-aminoethyl)(hydroxy)phosphoryl]-2-(N-(tert-butoxycarbonyl)amino)-3-O-methoxymethyl-15-(4'-benzoylphenyl)-(4E)-pentadecene-1,3-diol

Guidance literature:: Multi-step reaction with 6 steps

1.1: 92 percent / iPr₂NEt / CH₂Cl₂ / 0 - 20 °C

2.1: 9-BBN-H / tetrahydrofuran / 20 °C

2.2: 73 percent / Pd(PPh₃)4; K₃PO₄ / tetrahydrofuran; dioxane; H₂O / 85 °C

3.1: 88 percent / acetic acid / H₂O / 5 h / 80 °C

4.1: pyridine / diethyl ether / Heating

5.1: 206 mg / H₂O / diethyl ether / 20 °C

6.1: 85 percent / Et₃N; 1,3-propanedithiol / methanol / 20 °C

With pyridine; 1.3-propanedithiol; 9-borabicyclo[3.3.1]nonane dimer; water; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; 2.2: Suzuki coupling;
DOI:10.1021/jo050513u