1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid

Base Information

Chemical Name:1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid
CAS No.:100856-43-7
Molecular Formula:C₂₄H₂₂N₂O₃
Molecular Weight:386.45
Hs Code.:

Synonyms:1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid

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Chemical Property of 1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid

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Technology Process of 1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid

There total 7 articles about 1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid 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: 90.0%

: 100856-34-6
1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid ethyl ester

: 100856-43-7
1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid

Guidance literature:: With sodium hydroxide; In methanol; water; heating on a boiling water bath, 1 hr.,;
DOI:10.1002/jhet.5570220323

Reference yield:

: 100-39-0
benzyl bromide

: 100856-43-7
1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydride (60 percent) / tetrahydrofuran / 1.) reflux, 4 hrs., 2.) r.t., overnight

2: polyphosphoric ester / 2 h / 100 - 110 °C

3: 100 percent / sodium methoxide / dimethylformamide / r.t., overnight

4: 90 percent / sodium hydroxide (1 percent) / methanol; H₂O / heating on a boiling water bath, 1 hr.,

With sodium hydroxide; polyphosphoric ester; sodium methylate; sodium hydride; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570220323

Reference yield:

: 100856-21-1
N-<2-phenyl-5-methylpyrrol-3-yl>aminomethylenemalonic acid, diethyl ester

: 100856-43-7
1-Benzyl-6-ethyl-5-methyl-4-oxo-7-phenyl-4,6-dihydro-1H-pyrrolo[3,4-b]pyridine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydride (60 percent) / tetrahydrofuran / 1.) reflux, 4 hrs., 2.) r.t., overnight

2: polyphosphoric ester / 2 h / 100 - 110 °C

3: 100 percent / sodium methoxide / dimethylformamide / r.t., overnight

4: 90 percent / sodium hydroxide (1 percent) / methanol; H₂O / heating on a boiling water bath, 1 hr.,

With sodium hydroxide; polyphosphoric ester; sodium methylate; sodium hydride; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570220323