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ethyl 2-[5-chloro-2-[[2-(2,4-difluorophenoxy)-2-[4-(1-piperidylsulfonyl)phenyl]acetyl]amino]thiazol-4-yl]acetate

Base Information
  • Chemical Name:ethyl 2-[5-chloro-2-[[2-(2,4-difluorophenoxy)-2-[4-(1-piperidylsulfonyl)phenyl]acetyl]amino]thiazol-4-yl]acetate
  • CAS No.:1328984-14-0
  • Molecular Formula:C26H26ClF2N3O6S2
  • Molecular Weight:614.091
  • Hs Code.:
ethyl 2-[5-chloro-2-[[2-(2,4-difluorophenoxy)-2-[4-(1-piperidylsulfonyl)phenyl]acetyl]amino]thiazol-4-yl]acetate

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Chemical Property of ethyl 2-[5-chloro-2-[[2-(2,4-difluorophenoxy)-2-[4-(1-piperidylsulfonyl)phenyl]acetyl]amino]thiazol-4-yl]acetate
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Technology Process of ethyl 2-[5-chloro-2-[[2-(2,4-difluorophenoxy)-2-[4-(1-piperidylsulfonyl)phenyl]acetyl]amino]thiazol-4-yl]acetate

There total 5 articles about ethyl 2-[5-chloro-2-[[2-(2,4-difluorophenoxy)-2-[4-(1-piperidylsulfonyl)phenyl]acetyl]amino]thiazol-4-yl]acetate 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:
With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 18h; Cooling with ice; Inert atmosphere;
DOI:10.1016/j.ejmech.2017.03.042
Guidance literature:
Multi-step reaction with 6 steps
1.1: sulfuric acid / methanol / 24 h / 20 °C / Inert atmosphere
2.1: potassium nitrate; chloro-trimethyl-silane / dichloromethane / 50 °C / Sealed tube; Inert atmosphere
3.1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 48 h / Reflux; Inert atmosphere
3.2: 0 - 20 °C / Inert atmosphere
4.1: caesium carbonate / acetonitrile / 3.5 h / 25 °C / Inert atmosphere
5.1: lithium hydroxide / tetrahydrofuran; methanol; water / 18 h / 20 °C / Inert atmosphere
6.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; 4-methyl-morpholine / dichloromethane / 18 h / 20 °C / Cooling with ice; Inert atmosphere
With 4-methyl-morpholine; N-Bromosuccinimide; chloro-trimethyl-silane; sulfuric acid; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; potassium nitrate; lithium hydroxide; dibenzoyl peroxide; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane; water; acetonitrile;
DOI:10.1016/j.ejmech.2017.03.042
Guidance literature:
Multi-step reaction with 5 steps
1.1: potassium nitrate; chloro-trimethyl-silane / dichloromethane / 50 °C / Sealed tube; Inert atmosphere
2.1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 48 h / Reflux; Inert atmosphere
2.2: 0 - 20 °C / Inert atmosphere
3.1: caesium carbonate / acetonitrile / 3.5 h / 25 °C / Inert atmosphere
4.1: lithium hydroxide / tetrahydrofuran; methanol; water / 18 h / 20 °C / Inert atmosphere
5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; 4-methyl-morpholine / dichloromethane / 18 h / 20 °C / Cooling with ice; Inert atmosphere
With 4-methyl-morpholine; N-Bromosuccinimide; chloro-trimethyl-silane; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; potassium nitrate; lithium hydroxide; dibenzoyl peroxide; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane; water; acetonitrile;
DOI:10.1016/j.ejmech.2017.03.042
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