C₂₀H₁₉FN₄O₃

Base Information

Chemical Name:C₂₀H₁₉FN₄O₃
CAS No.:798563-57-2
Molecular Formula:C₂₀H₁₉FN₄O₃
Molecular Weight:382.394
Hs Code.:

C<sub>20</sub>H<sub>19</sub>FN<sub>4</sub>O<sub>3</sub>

Synonyms:C₂₀H₁₉FN₄O₃

Suppliers and Price of C₂₀H₁₉FN₄O₃

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 C₂₀H₁₉FN₄O₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₀H₁₉FN₄O₃

There total 10 articles about C₂₀H₁₉FN₄O₃ 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: 73.0%

: 798563-56-1
4-chloromethyl-1-(2-fluoro-5-methoxy-benzyl)-6,7-dimethoxy-isoquinoline

: 798563-57-2
C₂₀H₁₉FN₄O₃

Guidance literature:: With sodium azide; In dimethyl sulfoxide; at 65 ℃; for 2h;

Reference yield:

: 93-17-4
3,4-dimethoxyphenylacetonitrile

: 798563-57-2
C₂₀H₁₉FN₄O₃

Guidance literature:: Multi-step reaction with 8 steps

1.1: ethanol; sodium / toluene / 2 h / 80 - 85 °C

1.2: 2 h / 80 °C

2.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / ethanol; water / 2844.39 Torr

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 12 h / 20 °C

4.1: phosphorus pentachloride / dichloromethane / 2.5 h / 20 °C

5.1: sulfur / 0.33 h / 165 °C

6.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

7.1: methanesulfonyl chloride; triethylamine / dichloromethane / 2 h / 0 °C

7.2: 20 °C

8.1: sodium azide / dimethyl sulfoxide / 2 h / 65 °C

With hydrogenchloride; lithium aluminium tetrahydride; sodium azide; ethanol; phosphorus pentachloride; hydrogen; sodium; benzotriazol-1-ol; sulfur; methanesulfonyl chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; water; dimethyl sulfoxide; toluene;

Reference yield:

: 36848-69-8
ethyl 2-cyano-2-(3,4-dimethoxyphenyl)acetate

: 798563-57-2
C₂₀H₁₉FN₄O₃

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / ethanol; water / 2844.39 Torr

2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 12 h / 20 °C

3.1: phosphorus pentachloride / dichloromethane / 2.5 h / 20 °C

4.1: sulfur / 0.33 h / 165 °C

5.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

6.1: methanesulfonyl chloride; triethylamine / dichloromethane / 2 h / 0 °C

6.2: 20 °C

7.1: sodium azide / dimethyl sulfoxide / 2 h / 65 °C

With hydrogenchloride; lithium aluminium tetrahydride; sodium azide; phosphorus pentachloride; hydrogen; benzotriazol-1-ol; sulfur; methanesulfonyl chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; water; dimethyl sulfoxide;