E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one

Base Information

Chemical Name:E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one
CAS No.:1360822-00-9
Molecular Formula:C₁₅H₁₀ClFN₂O
Molecular Weight:288.709
Hs Code.:

Synonyms:E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one

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Chemical Property of E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one

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Technology Process of E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one

There total 1 articles about E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one 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: 58.0%

: 85070-48-0
2-fluoro-3-chlorobenzaldehyde

: 56057-25-1
7-methyl-1,3-dihydro-pyrrolo[3,2-b]pyridin-2-one

: 1360822-00-9
E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one

Guidance literature:: With piperidine; In methanol; at 50 ℃;

Reference yield: 26.0%

: 1345866-83-2
4-{2-[3,3-dimethyl-but-(E)-ylideneamino]acetylamino}-3-methoxybenzoic acid methyl ester

: 1360822-00-9
E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one

: methyl rac-4-((2S,3S,4S,5R)-4-(3-chloro-2-fluorophenyl)-7'-methyl-2-neopentyl-2'-oxo-1',2'-dihydrospiro[pyrrolidine-3,3'-pyrrolo[3,2-b]pyridine]-5-ylcarboxamido)-3-methoxybenzoate

Guidance literature:: E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one; With lithium hydroxide; In tetrahydrofuran; at 40 ℃; for 0.166667h;

4-{2-[3,3-dimethyl-but-(E)-ylideneamino]acetylamino}-3-methoxybenzoic acid methyl ester; In tetrahydrofuran; at 40 ℃; for 20h;

Reference yield:

: 1345866-83-2
4-{2-[3,3-dimethyl-but-(E)-ylideneamino]acetylamino}-3-methoxybenzoic acid methyl ester

: 1360822-00-9
E/Z-3-(3-chloro-2-fluorobenzylidene)-7-methyl-1,3-dihydropyrrolo[3,2-b]pyridin-2-one

: rac-4-((2S,3S,4S,5R)-4-(3-chloro-2-fluorophenyl)-7'-methyl-2-neopentyl-2'-oxo-1',2'-dihydrospiro[pyrrolidine-3,3'-pyrrolo[3,2-b]pyridine]-5-ylcarboxamido)-3-methoxybenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium hydroxide / tetrahydrofuran / 0.17 h / 40 °C

1.2: 20 h / 40 °C

2.1: lithium hydroxide monohydrate / tetrahydrofuran / 20 °C

With lithium hydroxide monohydrate; lithium hydroxide; In tetrahydrofuran;