N-(2-chloro-5-(2-chloro-4-(1,1-dioxidoisothiazolidin-2-yl)benzamido)phenyl)nicotinamide

Base Information

Chemical Name:N-(2-chloro-5-(2-chloro-4-(1,1-dioxidoisothiazolidin-2-yl)benzamido)phenyl)nicotinamide
CAS No.:1609355-66-9
Molecular Formula:C₂₂H₁₈Cl₂N₄O₄S
Molecular Weight:505.381
Hs Code.:

Synonyms:N-(2-chloro-5-(2-chloro-4-(1,1-dioxidoisothiazolidin-2-yl)benzamido)phenyl)nicotinamide

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Chemical Property of N-(2-chloro-5-(2-chloro-4-(1,1-dioxidoisothiazolidin-2-yl)benzamido)phenyl)nicotinamide

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Technology Process of N-(2-chloro-5-(2-chloro-4-(1,1-dioxidoisothiazolidin-2-yl)benzamido)phenyl)nicotinamide

There total 6 articles about N-(2-chloro-5-(2-chloro-4-(1,1-dioxidoisothiazolidin-2-yl)benzamido)phenyl)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: 34.0%

: 937392-56-8
N-(5-amino-2-chlorophenyl)nicotinamide

: 1292620-71-3
4-(1,1-dioxidoisothiazolidin-2-yl)-3-fluorobenzoic acid

: 1609355-66-9
N-(2-chloro-5-(2-chloro-4-(1,1-dioxidoisothiazolidin-2-yl)benzamido)phenyl)nicotinamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 17h;

Reference yield:

: 59-67-6
nicotinic acid

: 1609355-66-9
N-(2-chloro-5-(2-chloro-4-(1,1-dioxidoisothiazolidin-2-yl)benzamido)phenyl)nicotinamide

Guidance literature:: Multi-step reaction with 3 steps

1: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 20 °C

2: tin(II) chloride dihdyrate / ethanol / 16 h / 60 °C

3: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 17 h / 20 °C

With tin(II) chloride dihdyrate; N-ethyl-N,N-diisopropylamine; HATU; In ethanol; N,N-dimethyl-formamide;

Reference yield:

: 1609356-22-0
3-((3-chloro-4-(methoxycarbonyl)phenyl)amino)propane-1-sulfonic acid

: 1609355-66-9
N-(2-chloro-5-(2-chloro-4-(1,1-dioxidoisothiazolidin-2-yl)benzamido)phenyl)nicotinamide

Guidance literature:: Multi-step reaction with 3 steps

1: trichlorophosphate / 5 h / Reflux

2: lithium hydroxide; water / tetrahydrofuran; methanol / 8 h / 20 °C

3: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 17 h / 20 °C

With water; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; trichlorophosphate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;