methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate

Base Information

Chemical Name:methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate
CAS No.:1341232-06-1
Molecular Formula:C₂₂H₂₀ClFN₂O₄
Molecular Weight:430.863
Hs Code.:

Synonyms:methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate

Suppliers and Price of methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate

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 methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate

There total 5 articles about methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate 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: 81.0%

: 1341232-05-0
methyl 5,6-dichloro-2-(3-fluorophenyl)nicotinate

: 5763-61-1
3,4-dimethoxybenzylamine

: 1341232-06-1
methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate

Guidance literature:: In ethanol; for 0.5h; Reflux;

Reference yield:

: 67754-03-4
methyl 2,5-dichloronicotinate

: 1341232-06-1
methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane; water / 14.5 h / 80 °C / Inert atmosphere

2: peracetic acid / 1 h / 90 °C

3: trichlorophosphate / 1 h / 90 °C

4: ethanol / 0.5 h / Reflux

With peracetic acid; potassium carbonate; trichlorophosphate; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; ethanol; water;

Reference yield:

: 59782-85-3
2,5-dichloronicotinic acid

: 1341232-06-1
methyl 5-chloro-6-[(3,4-dimethoxybenzyl)amino]-2-(3-fluorophenyl)nicotinate

Guidance literature:: Multi-step reaction with 5 steps

1.1: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 18 h / 20 °C

1.2: 0.5 h / 0 °C

2.1: potassium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane; water / 14.5 h / 80 °C / Inert atmosphere

3.1: peracetic acid / 1 h / 90 °C

4.1: trichlorophosphate / 1 h / 90 °C

5.1: ethanol / 0.5 h / Reflux

With peracetic acid; oxalyl dichloride; potassium carbonate; N,N-dimethyl-formamide; trichlorophosphate; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; ethanol; dichloromethane; water;