{5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid

Base Information

Chemical Name:{5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid
CAS No.:1052721-38-6
Molecular Formula:C₂₁H₁₇ClF₂N₂O₆S₂
Molecular Weight:530.958
Hs Code.:

Synonyms:{5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid

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Chemical Property of {5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid

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Technology Process of {5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid

There total 7 articles about {5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid 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:

: 1052722-23-2
{5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid methyl ester

: 1052721-38-6
{5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid

Guidance literature:: {5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid methyl ester; With lithium hydroxide; ethanol; water; In tetrahydrofuran; at 20 ℃; for 5h;

With hydrogenchloride; water;

Reference yield:

: 300355-18-4
(4-methanesulfonyl-phenyl)-acetic acid methyl ester

: 1052721-38-6
{5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; n-butyllithium; diisopropylamine / tetrahydrofuran / 1.5 h / -78 °C

1.2: -78 - 20 °C

2.1: N-Bromosuccinimide / dibenzoyl peroxide / tetrachloromethane / 1 h / Heating / reflux

3.1: potassium carbonate / N,N-dimethyl-formamide / 2 - 3 h / 60 - 70 °C

4.1: methanol; sodium hydroxide; water / 20 °C

5.1: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

6.1: lithium hydroxide; ethanol; water / tetrahydrofuran / 5 h / 20 °C

With 4-methyl-morpholine; methanol; 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; lithium hydroxide; sodium hydroxide; N-Bromosuccinimide; n-butyllithium; ethanol; water; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; diisopropylamine; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1052722-20-9
2-(4-methanesulfonyl-phenyl)-propionic acid methyl ester

: 1052721-38-6
{5-chloro-2-[2-(2,4-difluoro-phenoxy)-2-(4-methanesulfonyl-phenyl)-propionylamino]-thiazol-4-yl}-acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: N-Bromosuccinimide / dibenzoyl peroxide / tetrachloromethane / 1 h / Heating / reflux

2: potassium carbonate / N,N-dimethyl-formamide / 2 - 3 h / 60 - 70 °C

3: methanol; sodium hydroxide; water / 20 °C

4: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

5: lithium hydroxide; ethanol; water / tetrahydrofuran / 5 h / 20 °C

With 4-methyl-morpholine; methanol; lithium hydroxide; sodium hydroxide; N-Bromosuccinimide; ethanol; water; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; dichloromethane; N,N-dimethyl-formamide;