2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide

Base Information

Chemical Name:2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide
CAS No.:1363178-98-6
Molecular Formula:C₂₆H₂₂N₂O₅S₂
Molecular Weight:506.603
Hs Code.:

Synonyms:2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide

Suppliers and Price of 2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide

There total 8 articles about 2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide 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:

: 1156632-48-2
{4-[(2-hydroxyethyl)sulfonyl]phenyl}acetic acid

: 17279-56-0
(2-amino-4-phenyl-1,3-thiazol-5-yl)(phenyl)methanone

: 1363178-98-6
2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; Inert atmosphere;

Reference yield:

: 91361-92-1
(4-mercapto-phenyl)-acetic acid methyl ester

: 1363178-98-6
2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 20 °C

2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 14 h / Cooling with ice

3.1: lithium hydroxide monohydrate / tetrahydrofuran / 20 °C

3.2: pH 1 - 2

4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C / Inert atmosphere

With lithium hydroxide monohydrate; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1197-55-3
4-aminophenylacetic acid

: 1363178-98-6
2-{4-[(2-hydroxyethyl)sulfonyl]phenyl}-N-[4-phenyl-5-(phenylcarbonyl)-1,3-thiazol-2-yl]acetamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: hydrogenchloride; sodium nitrite / water / 0.75 h / 0 °C

1.2: 20 - 45 °C

2.1: potassium hydroxide; water / ethanol / 20 h / Reflux

3.1: sulfuric acid / 0.75 h / 70 °C

3.2: 0 °C / pH 7

4.1: caesium carbonate / N,N-dimethyl-formamide / 20 °C

5.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 14 h / Cooling with ice

6.1: lithium hydroxide monohydrate / tetrahydrofuran / 20 °C

6.2: pH 1 - 2

7.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C / Inert atmosphere

With hydrogenchloride; lithium hydroxide monohydrate; sulfuric acid; water; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 3-chloro-benzenecarboperoxoic acid; potassium hydroxide; sodium nitrite; In tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide;