C₃₁H₃₀F₂N₆O₂

Base Information

Chemical Name:C₃₁H₃₀F₂N₆O₂
CAS No.:1418127-62-4
Molecular Formula:C₃₁H₃₀F₂N₆O₂
Molecular Weight:556.615
Hs Code.:

C<sub>31</sub>H<sub>30</sub>F<sub>2</sub>N<sub>6</sub>O<sub>2</sub>

Synonyms:C₃₁H₃₀F₂N₆O₂

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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 C₃₁H₃₀F₂N₆O₂

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Technology Process of C₃₁H₃₀F₂N₆O₂

There total 9 articles about C₃₁H₃₀F₂N₆O₂ 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:

: 946118-80-5
4-(1-fluoro-cyclopropyl)-benzoic acid

: 1418128-35-4
4-[4-(3-amino-5-fluoro-2-methyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-1-carboxylic acid dimethylamide

: 1418127-62-4
C₃₁H₃₀F₂N₆O₂

Guidance literature:: With 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl acetamide; at 20 ℃; for 18h;

Reference yield:

: 375853-82-0,286961-14-6
tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-1(2H)-pyridinecarboxylate

: 1418127-62-4
C₃₁H₃₀F₂N₆O₂

Guidance literature:: Multi-step reaction with 5 steps

1: sodium carbonate; bis-triphenylphosphine-palladium(II) chloride / propan-1-ol; water / 18 h / 100 °C

2: trifluoroacetic acid / water; dichloromethane / 2 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 h / 20 °C

4: sodium carbonate; bis-triphenylphosphine-palladium(II) chloride / propan-1-ol; water / 16 h / 100 °C

5: N-ethyl-N,N-diisopropylamine; 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate / N,N-dimethyl acetamide / 18 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; sodium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In propan-1-ol; dichloromethane; N,N-dimethyl acetamide; water; 1: |Suzuki Coupling / 4: |Suzuki Coupling;

Reference yield:

: 502496-33-5
1-bromo-5-fluoro-2-methyl-3-nitrobenzene

: 1418127-62-4
C₃₁H₃₀F₂N₆O₂

Guidance literature:: Multi-step reaction with 4 steps

1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate / 1,4-dioxane / 6 h / 100 °C

2: palladium 10% on activated carbon; hydrogen / ethyl acetate / 18 h / 20 °C / 760.05 Torr

3: sodium carbonate; bis-triphenylphosphine-palladium(II) chloride / propan-1-ol; water / 16 h / 100 °C

4: N-ethyl-N,N-diisopropylamine; 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate / N,N-dimethyl acetamide / 18 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; 1-[(1-(cyano-?2-?ethoxy-?2-?oxoethylidenaminooxy)?dimethylamino-?morpholino)]-uronium hexafluorophosphate; palladium 10% on activated carbon; hydrogen; potassium acetate; sodium carbonate; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; propan-1-ol; N,N-dimethyl acetamide; water; ethyl acetate; 3: |Suzuki Coupling;