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N-(2-(4-(6-(3-hydroxyphenyl)imidazo[2,1-b]thiazol-5-yl)pyrimidin-2-ylamino)ethyl)-3-(trifluoromethyl)-4-morpholinobenzamide

Base Information
  • Chemical Name:N-(2-(4-(6-(3-hydroxyphenyl)imidazo[2,1-b]thiazol-5-yl)pyrimidin-2-ylamino)ethyl)-3-(trifluoromethyl)-4-morpholinobenzamide
  • CAS No.:1350454-97-5
  • Molecular Formula:C29H26F3N7O3S
  • Molecular Weight:609.632
  • Hs Code.:
N-(2-(4-(6-(3-hydroxyphenyl)imidazo[2,1-b]thiazol-5-yl)pyrimidin-2-ylamino)ethyl)-3-(trifluoromethyl)-4-morpholinobenzamide

Synonyms:N-(2-(4-(6-(3-hydroxyphenyl)imidazo[2,1-b]thiazol-5-yl)pyrimidin-2-ylamino)ethyl)-3-(trifluoromethyl)-4-morpholinobenzamide

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Chemical Property of N-(2-(4-(6-(3-hydroxyphenyl)imidazo[2,1-b]thiazol-5-yl)pyrimidin-2-ylamino)ethyl)-3-(trifluoromethyl)-4-morpholinobenzamide
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Technology Process of N-(2-(4-(6-(3-hydroxyphenyl)imidazo[2,1-b]thiazol-5-yl)pyrimidin-2-ylamino)ethyl)-3-(trifluoromethyl)-4-morpholinobenzamide

There total 6 articles about N-(2-(4-(6-(3-hydroxyphenyl)imidazo[2,1-b]thiazol-5-yl)pyrimidin-2-ylamino)ethyl)-3-(trifluoromethyl)-4-morpholinobenzamide 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:
Guidance literature:
N-(2-(4-(6-(3-methoxyphenyl)imidazo[2,1-b]thiazol-5-yl)pyrimidin-2-ylamino)ethyl)-3-(trifluoromethyl)-4-morpholinobenzamide; With boron tribromide; In dichloromethane; at -78 - 20 ℃; for 1.5h; Inert atmosphere;
With water; sodium hydrogencarbonate; Saturated solution;
DOI:10.1016/j.ejmech.2011.08.024
Guidance literature:
Multi-step reaction with 3 steps
1.1: Oxone / methanol; water / 16 h / 20 °C
2.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 8 h / 80 °C
3.1: boron tribromide / dichloromethane / 1.5 h / -78 - 20 °C / Inert atmosphere
3.2: Saturated solution
With Oxone; boron tribromide; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; water; dimethyl sulfoxide;
DOI:10.1016/j.ejmech.2011.08.024
Guidance literature:
Multi-step reaction with 3 steps
1.1: palladium 10% on activated carbon; hydrogen / methanol / 1 h / 20 °C
2.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 8 h / 80 °C
3.1: boron tribromide / dichloromethane / 1.5 h / -78 - 20 °C / Inert atmosphere
3.2: Saturated solution
With palladium 10% on activated carbon; hydrogen; boron tribromide; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.ejmech.2011.08.024
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