N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-(azetidin-1-yl)pyrimidin-2-ylthio)phenyl)-2-chlorobenzamide

Base Information

Chemical Name:N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-(azetidin-1-yl)pyrimidin-2-ylthio)phenyl)-2-chlorobenzamide
CAS No.:1079394-20-9
Molecular Formula:C₂₂H₁₈ClN₇OS₂
Molecular Weight:496.016
Hs Code.:

Synonyms:N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-(azetidin-1-yl)pyrimidin-2-ylthio)phenyl)-2-chlorobenzamide

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Chemical Property of N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-(azetidin-1-yl)pyrimidin-2-ylthio)phenyl)-2-chlorobenzamide

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Technology Process of N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-(azetidin-1-yl)pyrimidin-2-ylthio)phenyl)-2-chlorobenzamide

There total 2 articles about N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-(azetidin-1-yl)pyrimidin-2-ylthio)phenyl)-2-chlorobenzamide 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:

: 503-29-7
azetidine

: 1079394-30-1
N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-chloropyrimidin-2-ylthio)phenyl)-2-chlorobenzamide

: 1079394-20-9
N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-(azetidin-1-yl)pyrimidin-2-ylthio)phenyl)-2-chlorobenzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 130 ℃; for 0.333333h;

Reference yield:

: 936560-20-2
2-chloro-N-(4-(4,6-dichloropyrimidin-2-ylthio)phenyl)benzamide

: 1079394-20-9
N-(4-(4-(1,2,4-thiadiazol-5-ylamino)-6-(azetidin-1-yl)pyrimidin-2-ylthio)phenyl)-2-chlorobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium carbonate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 2 h / 130 °C / Microwave irradiation

2: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 0.33 h / 130 °C

With sodium carbonate; N-ethyl-N,N-diisopropylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane;