N-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide

Base Information

Chemical Name:N-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide
CAS No.:214485-36-6
Molecular Formula:C₂₄H₂₃BrFN₅O
Molecular Weight:496.382
Hs Code.:

Synonyms:N-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide

Suppliers and Price of N-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide

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-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide

There total 8 articles about N-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide 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:

: 214485-53-7
6-Amino-4-[(3-Bromo-4-fluorophenyl)amino]-quinoline-3-carbonitrile

: 51544-74-2
4-bromocrotonic acid chloride

: 109-89-7
diethylamine

: 214485-36-6
N-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide

Guidance literature:: 6-Amino-4-[(3-Bromo-4-fluorophenyl)amino]-quinoline-3-carbonitrile; 4-bromocrotonic acid chloride; With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; N,N-dimethyl-formamide; at 0 ℃; for 1.33333h;

diethylamine; In tetrahydrofuran; N,N-dimethyl-formamide; at -78 ℃; for 3h;

Reference yield:

: 79-37-8
oxalyl dichloride

: 214485-53-7
6-Amino-4-[(3-Bromo-4-fluorophenyl)amino]-quinoline-3-carbonitrile

: 5-bromo-but-2-enoyl chloride

: 88239-39-8
γ-bromocrotonate de trimethylsilyle

: 109-89-7
diethylamine

: 214485-36-6
N-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 367-21-5
3-chloro-4-fluorophenylamine

: 214485-36-6
N-{4-[(3-bromo-4-fluorophenyl)amino]-3-cyano-6-quinolinyl}-4-diethylamino-2-butenamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanol / 3.5 h / Heating / reflux

2.1: iron; ammonium chloride / methanol; water / 4 h / Heating / reflux

3.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran; N,N-dimethyl-formamide / 1.33 h / 0 °C

3.2: 3 h / -78 °C

With iron; ammonium chloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide;