C₂₂H₂₄F₂N₄O₄

Base Information

Chemical Name:C₂₂H₂₄F₂N₄O₄
CAS No.:1079399-20-4
Molecular Formula:C₂₂H₂₄F₂N₄O₄
Molecular Weight:446.454
Hs Code.:

C<sub>22</sub>H<sub>24</sub>F<sub>2</sub>N<sub>4</sub>O<sub>4</sub>

Synonyms:C₂₂H₂₄F₂N₄O₄

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₂H₂₄F₂N₄O₄

Chemical Property:

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Technology Process of C₂₂H₂₄F₂N₄O₄

There total 5 articles about C₂₂H₂₄F₂N₄O₄ 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:

: 29578-39-0
1-bromo-3-fluoro-5-methoxybenzene

: 1079399-20-4
C₂₂H₂₄F₂N₄O₄

Guidance literature:: Multi-step reaction with 4 steps

1.1: magnesium / hydrogenchloride; iodine / diethyl ether / 1.5 h / 20 °C / Heating / reflux

1.2: 20 °C

2.1: boron tribromide / dichloromethane / 3 h / 0 °C

3.1: potassium carbonate / acetone / 20 °C

4.1: 2-hydroxypyridin; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 - 70 °C

With 2-hydroxypyridin; boron tribromide; potassium carbonate; magnesium; N-ethyl-N,N-diisopropylamine; hydrogenchloride; iodine; In diethyl ether; dichloromethane; acetone;

Reference yield:

: 1079398-67-6
5S-(1S-azido-2-hydroxyethyl)-3R-methoxydihydro furan-2-one

: 1079399-20-4
C₂₂H₂₄F₂N₄O₄

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / dichloromethane / 0.67 h / 0 °C

2: potassium carbonate / acetone / 20 °C

3: 2-hydroxypyridin; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 - 70 °C

With pyridine; 2-hydroxypyridin; potassium carbonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; acetone;

Reference yield:

: 951888-97-4
1-allyl-3-fluoro-5-methoxy-benzene

: 1079399-20-4
C₂₂H₂₄F₂N₄O₄

Guidance literature:: Multi-step reaction with 3 steps

1: boron tribromide / dichloromethane / 3 h / 0 °C

2: potassium carbonate / acetone / 20 °C

3: 2-hydroxypyridin; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 - 70 °C

With 2-hydroxypyridin; boron tribromide; potassium carbonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; acetone;