(3-amino-2-fluorophenyl)(5-bromo-1H-pyrrolo[2,3-b]pyridin- 3-yl)methanone

Base Information

Chemical Name:(3-amino-2-fluorophenyl)(5-bromo-1H-pyrrolo[2,3-b]pyridin- 3-yl)methanone
CAS No.:1254567-33-3
Molecular Formula:C₁₄H₉BrFN₃O
Molecular Weight:334.147
Hs Code.:

Synonyms:(3-amino-2-fluorophenyl)(5-bromo-1H-pyrrolo[2,3-b]pyridin- 3-yl)methanone

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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 (3-amino-2-fluorophenyl)(5-bromo-1H-pyrrolo[2,3-b]pyridin- 3-yl)methanone

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Technology Process of (3-amino-2-fluorophenyl)(5-bromo-1H-pyrrolo[2,3-b]pyridin- 3-yl)methanone

There total 6 articles about (3-amino-2-fluorophenyl)(5-bromo-1H-pyrrolo[2,3-b]pyridin- 3-yl)methanone 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: 76.0%

: 1312942-00-9
(5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl)(2-fluoro-3-nitrophenyl)methanone

: 1254567-33-3
(3-amino-2-fluorophenyl)(5-bromo-1H-pyrrolo[2,3-b]pyridin- 3-yl)methanone

Guidance literature:: With tin(II) chloride dihdyrate; In tetrahydrofuran; ethyl acetate; at 60 ℃;
DOI:10.1016/j.ejmech.2020.112963

Reference yield:

: 317-46-4
2-fluoro-3-nitro-benzoic acid

: 1254567-33-3
(3-amino-2-fluorophenyl)(5-bromo-1H-pyrrolo[2,3-b]pyridin- 3-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / N,N-dimethyl-formamide / 80 °C

2: aluminum (III) chloride / nitromethane / 6 h / 45 °C

3: tin(II) chloride dihdyrate / ethyl acetate; tetrahydrofuran / 72 h / 60 °C

With aluminum (III) chloride; thionyl chloride; tin(II) chloride dihdyrate; N,N-dimethyl-formamide; In tetrahydrofuran; nitromethane; ethyl acetate;

Reference yield:

: 96516-29-9
2-fluoro-3-nitrobenzaldehyde

: 1254567-33-3
(3-amino-2-fluorophenyl)(5-bromo-1H-pyrrolo[2,3-b]pyridin- 3-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1: water; aminosulfonic acid; sodium chlorite / 1,4-dioxane / 0.5 h / 20 °C

2: thionyl chloride / N,N-dimethyl-formamide / 80 °C

3: aluminum (III) chloride / nitromethane / 6 h / 45 °C

4: tin(II) chloride dihdyrate / ethyl acetate; tetrahydrofuran / 72 h / 60 °C

With aluminum (III) chloride; sodium chlorite; thionyl chloride; tin(II) chloride dihdyrate; aminosulfonic acid; water; N,N-dimethyl-formamide; In tetrahydrofuran; 1,4-dioxane; nitromethane; ethyl acetate;