6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide

Base Information

Chemical Name:6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide
CAS No.:1435685-96-3
Molecular Formula:C₂₂H₂₉BrN₄O₂
Molecular Weight:461.402
Hs Code.:

Synonyms:6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide

Suppliers and Price of 6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide

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 6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide

There total 6 articles about 6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide 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: 83.0%

: 6311-35-9
6-bromonicotinic acid

: 1435684-52-8
4-(4-(2-methoxyphenyl)-1,4-diazepan-1-yl)butan-1-amine

: 1435685-96-3
6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide

Guidance literature:: With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In dichloromethane; at 0 - 20 ℃; for 15h;
DOI:10.1016/j.bmc.2013.03.074

Reference yield:

: 112275-50-0
tert-butyl 1,4-diazepine-1-carboxylate

: 1435685-96-3
6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide

Guidance literature:: Multi-step reaction with 5 steps

1: 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; triethylamine; potassium tert-butylate / toluene / 21 h / 110 °C

2: trifluoroacetic acid / water / 20 °C

3: potassium carbonate / acetonitrile / Reflux; Inert atmosphere

4: hydrazine hydrate / ethanol / 2 h / Reflux

5: dicyclohexyl-carbodiimide; benzotriazol-1-ol / dichloromethane / 15 h / 0 - 20 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium tert-butylate; potassium carbonate; benzotriazol-1-ol; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; hydrazine hydrate; triethylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; In ethanol; dichloromethane; water; toluene; acetonitrile;
DOI:10.1016/j.bmc.2013.03.074

Reference yield:

: tert-Butyl 4-(2-methoxyphenyl)-1,4-diazepane-1-carboxylate

: 1435685-96-3
6-bromo-N-[4-[4-(2-methoxyphenyl)-1,4-diazepan-1-yl]butyl]nicotinamide

Guidance literature:: Multi-step reaction with 4 steps

1: trifluoroacetic acid / water / 20 °C

2: potassium carbonate / acetonitrile / Reflux; Inert atmosphere

3: hydrazine hydrate / ethanol / 2 h / Reflux

4: dicyclohexyl-carbodiimide; benzotriazol-1-ol / dichloromethane / 15 h / 0 - 20 °C

With potassium carbonate; benzotriazol-1-ol; hydrazine hydrate; dicyclohexyl-carbodiimide; trifluoroacetic acid; In ethanol; dichloromethane; water; acetonitrile;
DOI:10.1016/j.bmc.2013.03.074