(3-{7-oxo-6-[4-(trifluoromethoxy)benzyl]-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl}phenyl)formamide

Base Information

Chemical Name:(3-{7-oxo-6-[4-(trifluoromethoxy)benzyl]-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl}phenyl)formamide
CAS No.:1048678-16-5
Molecular Formula:C₂₂H₁₆F₃N₃O₃
Molecular Weight:427.383
Hs Code.:

Synonyms:(3-{7-oxo-6-[4-(trifluoromethoxy)benzyl]-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl}phenyl)formamide

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Chemical Property of (3-{7-oxo-6-[4-(trifluoromethoxy)benzyl]-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl}phenyl)formamide

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Technology Process of (3-{7-oxo-6-[4-(trifluoromethoxy)benzyl]-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl}phenyl)formamide

There total 6 articles about (3-{7-oxo-6-[4-(trifluoromethoxy)benzyl]-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl}phenyl)formamide 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: 41.0%

: 480425-37-4
N-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-formamide

: 1048678-22-3
3-bromo-6-[4-(trifluoromethoxy)benzyl]-5,6-dihydro-7H-pyrrolo[3,4-b]pyridin-7-one

: 1048678-16-5
(3-{7-oxo-6-[4-(trifluoromethoxy)benzyl]-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl}phenyl)formamide

Guidance literature:: With potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In N,N-dimethyl-formamide; at 110 ℃; for 1.5h;

Reference yield:

: 3430-18-0,141315-43-7
2,5-dibromo-3-methylpyridine

: 1048678-16-5
(3-{7-oxo-6-[4-(trifluoromethoxy)benzyl]-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl}phenyl)formamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: N,N-dimethyl-formamide / 12 h / 120 °C

2.1: sodium hydroxide; water / 1.5 h / 80 °C

2.2: pH 2 - 3 / Acidic aqueous solution

3.1: potassium carbonate / N,N-dimethyl-formamide / 0.67 h / 80 °C

4.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 5 h / 80 °C

5.1: potassium carbonate / toluene / 3 h / Heating / reflux

6.1: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 1.5 h / 110 °C

With sodium hydroxide; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); water; potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrachloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 213771-32-5
5-bromo-3-methylpyridine-2-carboxylic acid methyl ester

: 1048678-16-5
(3-{7-oxo-6-[4-(trifluoromethoxy)benzyl]-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-3-yl}phenyl)formamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 5 h / 80 °C

2: potassium carbonate / toluene / 3 h / Heating / reflux

3: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide / 1.5 h / 110 °C

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrachloromethane; N,N-dimethyl-formamide; toluene;