(S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate

Base Information

Chemical Name:(S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate
CAS No.:1338789-82-4
Molecular Formula:C₄₅H₃₇FN₃O₁₄P
Molecular Weight:893.773
Hs Code.:

Synonyms:(S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate

Suppliers and Price of (S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate

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 (S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate

There total 10 articles about (S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate 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: 74.0%

: 1338789-80-2
(S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(hydroxymethyl)-2-oxo-2H-chromen-4-yl)propanoate

: 1338789-82-4
(S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate

Guidance literature:: With diethylamino-sulfur trifluoride; In dichloromethane; at 0 ℃; for 0.166667h; Inert atmosphere;
DOI:10.1039/c1cc14653j

Reference yield:

: 1338789-72-2
(S)-allyl 6-methyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-oxohexanedioate

: 1338789-82-4
(S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: methanesulfonic acid / 4 h / 4 °C / Cooling with ice

2.1: acetic acid / 3 h / 100 - 150 °C

2.2: 1 h

3.1: dmap; triethylamine / dichloromethane / 5 h / Cooling with ice

4.1: sodium tetrahydroborate / ethanol; dichloromethane / 0.08 h / 0 °C

5.1: diethylamino-sulfur trifluoride / dichloromethane / 0.17 h / 0 °C / Inert atmosphere

With dmap; sodium tetrahydroborate; methanesulfonic acid; diethylamino-sulfur trifluoride; acetic acid; triethylamine; In ethanol; dichloromethane; 2.1: Duff reaction / 2.2: Duff reaction;
DOI:10.1039/c1cc14653j

Reference yield:

: 1338789-76-6
(S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(8-formyl-7-hydroxy-2-oxo-2H-chromen-4-yl)propanoate

: 1338789-82-4
(S)-allyl 2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(7-(bis(2-nitrobenzyloxy)phosphoryloxy)-8-(fluoromethyl)-2-oxo-2H-chromen-4-yl)propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: dmap; triethylamine / dichloromethane / 5 h / Cooling with ice

2: sodium tetrahydroborate / ethanol; dichloromethane / 0.08 h / 0 °C

3: diethylamino-sulfur trifluoride / dichloromethane / 0.17 h / 0 °C / Inert atmosphere

With dmap; sodium tetrahydroborate; diethylamino-sulfur trifluoride; triethylamine; In ethanol; dichloromethane;
DOI:10.1039/c1cc14653j