2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide

Base Information

Chemical Name:2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide
CAS No.:1313220-03-9
Molecular Formula:C₂₄H₂₀Cl₂N₄O₃S
Molecular Weight:515.42
Hs Code.:

Synonyms:2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide

Suppliers and Price of 2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide

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 2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide

There total 7 articles about 2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide 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: 13.0%

: 6579-54-0
2,6-dichlorobenzenesulfonyl chloride

: 1313220-02-8
(3-Aminomethyl-phenyl)-[6-(2-methoxy-phenyl)-pyrimidin-4-yl]-amine hydrochloride

: 1313220-03-9
2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃;

Reference yield: 13.0%

: 6579-54-0
2,6-dichlorobenzenesulfonyl chloride

: (3-aminomethyl-phenyl)-[6-(2-methoxy-phenyl)-pyrimidin-4-yl]-amine hydrochloride

: 1313220-03-9
2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide

Guidance literature:: (3-aminomethyl-phenyl)-[6-(2-methoxy-phenyl)-pyrimidin-4-yl]-amine hydrochloride; With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 0.25h;

2,6-dichlorobenzenesulfonyl chloride; In dichloromethane; at 0 - 20 ℃;

With sodium hydrogencarbonate; In dichloromethane;

Reference yield:

: 21081-63-0
2-(3-nitrobenzyl)isoindoline-1,3-dione

: 1313220-03-9
2,6-Dichloro-N-{3-[6-(2-methoxy-phenyl)-pyrimidin-4-ylamino]-benzyl}-benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: tin(II) chloride dihdyrate / ethanol / 6 h / Reflux

1.2: 0.5 h / Cooling with ice

2.1: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 96 h / Reflux

3.1: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 6 h / Inert atmosphere

4.1: hydrazine hydrate / ethanol / 2 h / Reflux

5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

With potassium phosphate; tin(II) chloride dihdyrate; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In ethanol; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol;