C₂₉H₂₆F₃N₃O₄

Base Information

Chemical Name:C₂₉H₂₆F₃N₃O₄
CAS No.:1616341-63-9
Molecular Formula:C₂₉H₂₆F₃N₃O₄
Molecular Weight:537.538
Hs Code.:

C<sub>29</sub>H<sub>26</sub>F<sub>3</sub>N<sub>3</sub>O<sub>4</sub>

Synonyms:C₂₉H₂₆F₃N₃O₄

Suppliers and Price of C₂₉H₂₆F₃N₃O₄

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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 C₂₉H₂₆F₃N₃O₄

Chemical Property:

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Technology Process of C₂₉H₂₆F₃N₃O₄

There total 11 articles about C₂₉H₂₆F₃N₃O₄ 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:

: 214759-21-4
(2,4,6-trifluorophenyl)methanamine

: 1616342-38-1
C₂₂H₂₂N₂O₅

: 1616341-63-9
C₂₉H₂₆F₃N₃O₄

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

Reference yield:

: C₁₄H₂₃NO₅

: 1616341-63-9
C₂₉H₂₆F₃N₃O₄

Guidance literature:: Multi-step reaction with 10 steps

1.1: Dess-Martin periodane / dichloromethane / 18 h / 20 °C / Cooling with ice

2.1: tetrahydrofuran / 2 h / 0 - 20 °C

3.1: hydrogen; palladium on activated charcoal / ethanol / 3 h

4.1: lithium borohydride / tetrahydrofuran / 3 h / -78 - 20 °C

5.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C

6.1: hydrazine hydrate / ethanol / 3 h / 70 °C

7.1: sodium hydrogencarbonate / ethanol; water / 20 °C

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

8.2: 1 h / 110 °C

9.1: potassium hydroxide; methanol / tetrahydrofuran / 1 h / 20 °C

10.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 2 h / 20 °C

With hydrogenchloride; methanol; lithium borohydride; di-isopropyl azodicarboxylate; palladium on activated charcoal; hydrogen; sodium hydrogencarbonate; Dess-Martin periodane; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water;

Reference yield:

: 1616341-55-9
C₁₃H₁₉NO₅

: 1616341-63-9
C₂₉H₂₆F₃N₃O₄

Guidance literature:: Multi-step reaction with 9 steps

1.1: tetrahydrofuran / 2 h / 0 - 20 °C

2.1: hydrogen; palladium on activated charcoal / ethanol / 3 h

3.1: lithium borohydride / tetrahydrofuran / 3 h / -78 - 20 °C

4.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C

5.1: hydrazine hydrate / ethanol / 3 h / 70 °C

6.1: sodium hydrogencarbonate / ethanol; water / 20 °C

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

7.2: 1 h / 110 °C

8.1: potassium hydroxide; methanol / tetrahydrofuran / 1 h / 20 °C

9.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 2 h / 20 °C

With hydrogenchloride; methanol; lithium borohydride; di-isopropyl azodicarboxylate; palladium on activated charcoal; hydrogen; sodium hydrogencarbonate; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water;