2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel

Base Information

Chemical Name:2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel
CAS No.:618887-03-9
Molecular Formula:C₆₂H₈₈INO₁₄Si₂
Molecular Weight:1254.45
Hs Code.:

2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel

Synonyms:2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel

Suppliers and Price of 2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel

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 2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel

There total 10 articles about 2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel 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: 78.0%

: 618886-92-3
(3R,4S)-1-(3-ethenylbenzoyl)-3-triisopropylsilyloxy-4-(3-butenyl)azetidin-2-one

: 618886-91-2
7-triethylsilyl-2-debenzoyl-2-(3-iodobenzoyl)baccatin III

: 618887-03-9
2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; at -40 ℃; for 0.583333h;
DOI:10.1021/ol0354627

Reference yield:

: 1711-10-0
3-iodobenzoyl chloride

: 618887-03-9
2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / Et₃N; DMAP / CH₂Cl₂ / 20 h / 20 °C

2: 86 percent / PPh₃ / Pd₂(dba)3 / dioxane / 48 h / 50 °C

3: 78 percent / LiHMDS / tetrahydrofuran / 0.58 h / -40 °C

With dmap; triethylamine; triphenylphosphine; lithium hexamethyldisilazane; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; dichloromethane; 3: Ojima-Holton β-lactam ring-opening coupling;
DOI:10.1021/ol0354627

Reference yield:

: 178250-09-4
(3R,4S)-3-triisopropylsilyloxy-4-(2-methylpropen-2-yl)azetidin-2-one

: 618887-03-9
2-debenzoyl-2-(3-iodobenzoyl)-3'-dephenyl-3'-(2-methylprop-1-enyl)-3'N-debenzoyl-3'N-(3-ethenylbenzoyl)-2'-triisopropylsilyl-7-triethylsilylpaclitaxel

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / Et₃N; DMAP / CH₂Cl₂ / 20 h / 20 °C

2: 86 percent / PPh₃ / Pd₂(dba)3 / dioxane / 48 h / 50 °C

3: 78 percent / LiHMDS / tetrahydrofuran / 0.58 h / -40 °C

With dmap; triethylamine; triphenylphosphine; lithium hexamethyldisilazane; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; dichloromethane; 3: Ojima-Holton β-lactam ring-opening coupling;
DOI:10.1021/ol0354627