C₂₈H₂₇BrF₄N₄O₅

Base Information

Chemical Name:C₂₈H₂₇BrF₄N₄O₅
CAS No.:869984-48-5
Molecular Formula:C₂₈H₂₇BrF₄N₄O₅
Molecular Weight:655.444
Hs Code.:

C<sub>28</sub>H<sub>27</sub>BrF<sub>4</sub>N<sub>4</sub>O<sub>5</sub>

Synonyms:C₂₈H₂₇BrF₄N₄O₅

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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 C₂₈H₂₇BrF₄N₄O₅

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Technology Process of C₂₈H₂₇BrF₄N₄O₅

There total 13 articles about C₂₈H₂₇BrF₄N₄O₅ 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:

: 869984-51-0
C₂₆H₂₆BrF₄N₃O₅

: 107-14-2
chloroacetonitrile

: 869984-48-5
C₂₈H₂₇BrF₄N₄O₅

Guidance literature:: With potassium carbonate; In DMF (N,N-dimethyl-formamide); at 60 ℃; for 16h;

Reference yield:

: 62717-78-6,141303-38-0
2-(2-methoxyphenyl)oxirane

: 869984-48-5
C₂₈H₂₇BrF₄N₄O₅

Guidance literature:: Multi-step reaction with 7 steps

1: sodium azide / water; acetone / 3 h / Heating / reflux

2: hydrogen / palladium 10% on activated carbon / ethanol / 20 °C

3: dichloromethane / 20 °C

4: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran

5: boron tribromide / dichloromethane / -70 - 20 °C

6: triethylamine / dichloromethane / 24 h / 20 °C

7: potassium carbonate / DMF (N,N-dimethyl-formamide) / 16 h / 60 °C

With sodium azide; di-isopropyl azodicarboxylate; hydrogen; boron tribromide; potassium carbonate; triethylamine; triphenylphosphine; palladium 10% on activated carbon; In tetrahydrofuran; DMF (N,N-dimethyl-formamide); ethanol; dichloromethane; water; acetone;

Reference yield:

: 135-02-4
ortho-anisaldehyde

: 869984-48-5
C₂₈H₂₇BrF₄N₄O₅

Guidance literature:: Multi-step reaction with 8 steps

1: sodium hydroxide; water; tetra-(n-butyl)ammonium iodide / dichloromethane / 168 h / 20 °C

2: sodium azide / water; acetone / 3 h / Heating / reflux

3: hydrogen / palladium 10% on activated carbon / ethanol / 20 °C

4: dichloromethane / 20 °C

5: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran

6: boron tribromide / dichloromethane / -70 - 20 °C

7: triethylamine / dichloromethane / 24 h / 20 °C

8: potassium carbonate / DMF (N,N-dimethyl-formamide) / 16 h / 60 °C

With sodium hydroxide; sodium azide; di-isopropyl azodicarboxylate; water; hydrogen; boron tribromide; tetra-(n-butyl)ammonium iodide; potassium carbonate; triethylamine; triphenylphosphine; palladium 10% on activated carbon; In tetrahydrofuran; DMF (N,N-dimethyl-formamide); ethanol; dichloromethane; water; acetone;