N-(1-(4-[3-(2,3-dichlorophenyl)urea]phenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide

Base Information

Chemical Name:N-(1-(4-[3-(2,3-dichlorophenyl)urea]phenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide
CAS No.:1314863-24-5
Molecular Formula:C₂₇H₁₉Cl₂N₅O₂
Molecular Weight:516.386
Hs Code.:

Synonyms:N-(1-(4-[3-(2,3-dichlorophenyl)urea]phenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide

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Chemical Property of N-(1-(4-[3-(2,3-dichlorophenyl)urea]phenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide

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Technology Process of N-(1-(4-[3-(2,3-dichlorophenyl)urea]phenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide

There total 7 articles about N-(1-(4-[3-(2,3-dichlorophenyl)urea]phenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide 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: 26.0%

: 1314863-22-3
N-(1-(4-aminophenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide

: 41195-90-8
1,2-dichloro-3-isocyanatobenzene

: 1314863-24-5
N-(1-(4-[3-(2,3-dichlorophenyl)urea]phenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide

Guidance literature:: In tetrahydrofuran; at 20 ℃; for 8h; Inert atmosphere;
DOI:10.1016/j.ejmech.2011.04.031

Reference yield:

: 55052-28-3
4-chloro-7-azaindole

: 1314863-24-5
N-(1-(4-[3-(2,3-dichlorophenyl)urea]phenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 180 °C

2: diisopropylamine / acetonitrile / 8 h / 20 °C / Inert atmosphere

3: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 2 h / 20 °C

4: tetrahydrofuran / 8 h / 20 °C / Inert atmosphere

With palladium 10% on activated carbon; hydrogen; diisopropylamine; In tetrahydrofuran; acetonitrile;
DOI:10.1016/j.ejmech.2011.04.031

Reference yield:

: 271-63-6
7-Azaindole

: 1314863-24-5
N-(1-(4-[3-(2,3-dichlorophenyl)urea]phenyl)-1H-pyrrolo[3,2-c]pyridin-4-yl)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: 1,2-dimethoxyethane; n-heptane / 20 °C

2: trichlorophosphate / 20 - 90 °C

3: 180 °C

4: diisopropylamine / acetonitrile / 8 h / 20 °C / Inert atmosphere

5: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 2 h / 20 °C

6: tetrahydrofuran / 8 h / 20 °C / Inert atmosphere

With palladium 10% on activated carbon; hydrogen; diisopropylamine; trichlorophosphate; In tetrahydrofuran; 1,2-dimethoxyethane; n-heptane; acetonitrile;
DOI:10.1016/j.ejmech.2011.04.031