tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate

Base Information

Chemical Name:tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate
CAS No.:1384485-43-1
Molecular Formula:C₂₅H₂₃ClN₄O₃
Molecular Weight:462.936
Hs Code.:

Synonyms:tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate

Suppliers and Price of tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate

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 tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate

There total 8 articles about tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate 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: 74.0%

: 1384485-42-0
tert-butyl [2-({4-[3-cyano-5-(morpholin-4-ylmethyl)pyridin-2-yl]benzoyl}amino)phenyl]carbamate

: 1384485-43-1
tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate

Guidance literature:: With chloroformic acid ethyl ester; In tetrahydrofuran; for 18h; Reflux;
DOI:10.1021/op300021m

Reference yield:

: 617703-01-2
N-(2-(tert-butoxycarbonylamino)phenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

: 1384485-43-1
tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane; water / 4 h / 80 °C / Alkaline conditions; Inert atmosphere

2: chloroformic acid ethyl ester / tetrahydrofuran / 18 h / Reflux

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; chloroformic acid ethyl ester; In tetrahydrofuran; 1,2-dimethoxyethane; water; 1: Suzuki coupling;
DOI:10.1021/op300021m

Reference yield:

: 146651-75-4
tert–butyl (2–aminophenyl)carbamate

: 1384485-43-1
tert-butyl [2-({4-[5-(chloromethyl)-3-cyanopyridin-2-yl]benzoyl}amino)phenyl]carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: 4-methyl-morpholine; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine / acetonitrile / 20 °C

2: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,2-dimethoxyethane; water / 4 h / 80 °C / Alkaline conditions; Inert atmosphere

3: chloroformic acid ethyl ester / tetrahydrofuran / 18 h / Reflux

With 4-methyl-morpholine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; chloroformic acid ethyl ester; In tetrahydrofuran; 1,2-dimethoxyethane; water; acetonitrile; 2: Suzuki coupling;
DOI:10.1021/op300021m