C₄₅H₄₃N₉O₆

Base Information

Chemical Name:C₄₅H₄₃N₉O₆
CAS No.:1242087-58-6
Molecular Formula:C₄₅H₄₃N₉O₆
Molecular Weight:805.893
Hs Code.:

C<sub>45</sub>H<sub>43</sub>N<sub>9</sub>O<sub>6</sub>

Synonyms:C₄₅H₄₃N₉O₆

Suppliers and Price of C₄₅H₄₃N₉O₆

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 C₄₅H₄₃N₉O₆

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₅H₄₃N₉O₆

There total 6 articles about C₄₅H₄₃N₉O₆ 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:

: 1242094-05-8
C₂₅H₂₅N₇

: 50890-96-5
(2R)-2-[(methoxycarbonyl)amino]-2-phenylacetic acid

: 1242087-58-6
C₄₅H₄₃N₉O₆

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

Reference yield:

: 15761-39-4,59433-50-0
1-(tert-butoxycarbonyl)-L-proline

: 1242087-58-6
C₄₅H₄₃N₉O₆

Guidance literature:: Multi-step reaction with 6 steps

1.1: chloroformic acid ethyl ester; triethylamine / tetrahydrofuran / 0.5 h / -20 °C

1.2: -20 - 20 °C

1.3: 2 h / 50 °C

2.1: copper(l) iodide; triethylamine / trans-bis(triphenylphosphine)palladium dichloride / 80 °C / Inert atmosphere

3.1: potassium carbonate / methanol / 2 h / 20 °C

4.1: copper(l) iodide; triethylamine / trans-bis(triphenylphosphine)palladium dichloride / acetonitrile / 3 h / 50 °C / Inert atmosphere

5.1: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

6.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 2 h / 20 °C

With hydrogenchloride; copper(l) iodide; chloroformic acid ethyl ester; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; trans-bis(triphenylphosphine)palladium dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1208007-67-3
1,1-dimethylethyl (2S)-2-(5-bromo-1H-benzimidazol-2-yl)-1-pyrrolidinecarboxylate

: 1242087-58-6
C₄₅H₄₃N₉O₆

Guidance literature:: Multi-step reaction with 5 steps

1: copper(l) iodide; triethylamine / trans-bis(triphenylphosphine)palladium dichloride / 80 °C / Inert atmosphere

2: potassium carbonate / methanol / 2 h / 20 °C

3: copper(l) iodide; triethylamine / trans-bis(triphenylphosphine)palladium dichloride / acetonitrile / 3 h / 50 °C / Inert atmosphere

4: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

5: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 2 h / 20 °C

With hydrogenchloride; copper(l) iodide; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; trans-bis(triphenylphosphine)palladium dichloride; In 1,4-dioxane; methanol; N,N-dimethyl-formamide; acetonitrile;