4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide

Base Information

Chemical Name:4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide
CAS No.:1401449-61-3
Molecular Formula:C₁₈H₁₇BrN₄O
Molecular Weight:385.263
Hs Code.:

Synonyms:4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide

Suppliers and Price of 4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide

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 4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide

There total 7 articles about 4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide 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: 50.0%

: 1360899-50-8
6-bromo-1H-1,3-benzodiazol-4-amine

: 1365243-78-2
[4-(cyclopropylcarbamoyl)-3-methylphenyl]boronic acid

: 1401449-61-3
4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide

Guidance literature:: With pyridine; pyridine N-oxide; copper diacetate; In dichloromethane; at 20 - 40 ℃; Inert atmosphere;

Reference yield:

: 68837-59-2
4-bromo-2-methylbenzoic acid

: 1401449-61-3
4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

2: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / 1,4-dioxane / 6 h / Reflux

3: sodium periodate; ammonium acetate / water; acetone / 20 - 40 °C

4: pyridine N-oxide; pyridine; copper diacetate / dichloromethane / 20 - 40 °C / Inert atmosphere

With pyridine; pyridine N-oxide; sodium periodate; ammonium acetate; copper diacetate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; In 1,4-dioxane; dichloromethane; water; acetone;

Reference yield:

: 345965-99-3
4-bromo-N-cyclopropyl-2-methylbenzamide

: 1401449-61-3
4-(4-amino-6-bromo-1H-benzimidazol-1-yl)-N-cyclopropyl-2-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos / 1,4-dioxane / 6 h / Reflux

2: sodium periodate; ammonium acetate / water; acetone / 20 - 40 °C

3: pyridine N-oxide; pyridine; copper diacetate / dichloromethane / 20 - 40 °C / Inert atmosphere

With pyridine; pyridine N-oxide; sodium periodate; ammonium acetate; copper diacetate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; In 1,4-dioxane; dichloromethane; water; acetone;