N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester

Base Information

Chemical Name:N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester
CAS No.:333362-83-7
Molecular Formula:C₄₈H₅₉N₆O₁₈P
Molecular Weight:1039
Hs Code.:

N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester

Synonyms:N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester

Suppliers and Price of N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester

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 N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester

There total 7 articles about N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester 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:

: 2-{3-{[3-acetoxy-5-(4-allyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethoxy]-allyloxy-phosphanyloxy}-2-[3-methyl-2-(4-phenylacetoxy-benzyloxycarbonylamino)-butyrylamino]-propionylamino}-propionic acid allyl ester

: 333362-83-7
N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester

Guidance literature:: With tert.-butylhydroperoxide; In dichloromethane; acetonitrile; at 0 ℃; for 0.166667h;
DOI:10.1002/1521-3765(20020415)8:8<1879::AID-CHEM1879>3.0.CO;2-5

Reference yield:

: 192999-59-0
PhAcOZ-Val-OH

: 333362-83-7
N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / HATU; DIPEA / dimethylformamide / 1 h / 0 °C

2: (iPr)2NH; tetrazole / CH₂Cl₂ / 1 h / 0 °C

3: terazole / acetonitrile; CH₂Cl₂ / 24 h / 20 °C

4: t-BuOOH / acetonitrile; CH₂Cl₂ / 0.17 h / 0 °C

With 1H-tetrazole; tert.-butylhydroperoxide; terazole; diisopropylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/1521-3765(20020415)8:8<1879::AID-CHEM1879>3.0.CO;2-5

Reference yield:

: 357625-71-9
{1-[(2R,4S,5R)-5-(tert-Butyl-dimethyl-silanyloxymethyl)-4-hydroxy-tetrahydro-furan-2-yl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-carbamic acid allyl ester

: 333362-83-7
N-phenylacetoxybenzyloxycarbonyl-L-valinyl-L-seryl-O-(3'-O-acetyl-6-N-allyloxycarbonyl-2'-deoxycytidyl-allyl-phosphato)-L-alanine allyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / pyridine / 3 h / 20 °C

2: 98 percent / Bu₄NF / tetrahydrofuran / 3 h / 20 °C

3: terazole / acetonitrile; CH₂Cl₂ / 24 h / 20 °C

4: t-BuOOH / acetonitrile; CH₂Cl₂ / 0.17 h / 0 °C

With pyridine; tert.-butylhydroperoxide; terazole; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1002/1521-3765(20020415)8:8<1879::AID-CHEM1879>3.0.CO;2-5