N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide

Base Information

Chemical Name:N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide
CAS No.:1415125-23-3
Molecular Formula:C₁₉H₁₄BrCl₂N₃O₂
Molecular Weight:467.149
Hs Code.:

Synonyms:N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide

Suppliers and Price of N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide

There total 6 articles about N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide 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:

: 1415123-73-7
N-{1-[2,6-dichloro-4-(hydroxymethyl)benzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide

: 1415125-23-3
N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide

Guidance literature:: With phosphorus tribromide; In dichloromethane; at 0 - 20 ℃; for 2h;

Reference yield:

: 5372-81-6
dimethyl aminoterephthalate

: 1415125-23-3
N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sulfuryl dichloride / diethyl ether / 15 h / 0 - 20 °C

2.1: sulfuric acid; sodium nitrite; acetic acid; phosphinic acid

3.1: sodium tetrahydroborate; methanol / tetrahydrofuran

4.1: pyridine; lithium iodide / 5 h / Reflux

5.1: dmap; N,N-dimethyl-aniline; 1-hydroxy-7-aza-benzotriazole; HATU

5.2: 15 h / 20 °C

6.1: phosphorus tribromide / dichloromethane / 2 h / 0 - 20 °C

With pyridine; methanol; dmap; sodium tetrahydroborate; phosphinic acid; sulfuryl dichloride; 1-hydroxy-7-aza-benzotriazole; sulfuric acid; phosphorus tribromide; acetic acid; N,N-dimethyl-aniline; HATU; lithium iodide; sodium nitrite; In tetrahydrofuran; diethyl ether; dichloromethane;

Reference yield:

: 264276-14-4
dimethyl 2,6-dichlorobenzene-1,4-dicarboxylate

: 1415125-23-3
N-{1-[4-(bromomethyl)-2,6-dichlorobenzoyl]-1H-pyrrolo[3,2-c]pyridin-4-yl}cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium tetrahydroborate; methanol / tetrahydrofuran

2.1: pyridine; lithium iodide / 5 h / Reflux

3.1: dmap; N,N-dimethyl-aniline; 1-hydroxy-7-aza-benzotriazole; HATU

3.2: 15 h / 20 °C

4.1: phosphorus tribromide / dichloromethane / 2 h / 0 - 20 °C

With pyridine; methanol; dmap; sodium tetrahydroborate; 1-hydroxy-7-aza-benzotriazole; phosphorus tribromide; N,N-dimethyl-aniline; HATU; lithium iodide; In tetrahydrofuran; dichloromethane;