3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine

Base Information

Chemical Name:3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine
CAS No.:221895-87-0
Molecular Formula:C₂₇H₃₄N₄O₁₁
Molecular Weight:590.587
Hs Code.:

Synonyms:3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine

Suppliers and Price of 3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine

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 3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine

There total 4 articles about 3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine 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: 88.0%

: 221895-84-7
3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>-5'-O-(tert-butyldiphenylsilyl)thymidine

: 221895-87-0
3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 25 ℃; for 0.25h;
DOI:10.1002/(SICI)1521-3765(19990301)5:3<951::AID-CHEM951>3.0.CO;2-G

Reference yield:

: 55715-03-2
4-bromomethyl-3-nitrobenzoic acid

: 221895-87-0
3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine

Guidance literature:: Multi-step reaction with 4 steps

1: oxalyl chloride, DMF / CH₂Cl₂ / 3 h / 0 °C

2: NEt₃, DMAP / CH₂Cl₂ / 3 h

3: 54 percent / Bu₄NOH, NaI, NaOH, H₂O / CH₂Cl₂ / 17 h / 25 °C

4: 88 percent / TBAF / tetrahydrofuran / 0.25 h / 25 °C

With dmap; sodium hydroxide; oxalyl dichloride; tetrabutyl ammonium fluoride; tetra(n-butyl)ammonium hydroxide; water; triethylamine; N,N-dimethyl-formamide; sodium iodide; In tetrahydrofuran; dichloromethane;
DOI:10.1002/(SICI)1521-3765(19990301)5:3<951::AID-CHEM951>3.0.CO;2-G

Reference yield:

: 73674-47-2
3-nitro-4-bromomethylbenzoyl chloride

: 221895-87-0
3'-O-<(4''-(N-allyloxycarbonyl)-5'''-aminopent-1-yl-oxycarbonyl)-2''-nitrophenylmethyl>thymidine

Guidance literature:: Multi-step reaction with 3 steps

1: NEt₃, DMAP / CH₂Cl₂ / 3 h

2: 54 percent / Bu₄NOH, NaI, NaOH, H₂O / CH₂Cl₂ / 17 h / 25 °C

3: 88 percent / TBAF / tetrahydrofuran / 0.25 h / 25 °C

With dmap; sodium hydroxide; tetrabutyl ammonium fluoride; tetra(n-butyl)ammonium hydroxide; water; triethylamine; sodium iodide; In tetrahydrofuran; dichloromethane;
DOI:10.1002/(SICI)1521-3765(19990301)5:3<951::AID-CHEM951>3.0.CO;2-G