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Acetamide, 2-[2-(2-bromobenzoyl)-4-chlorophenoxy]-N-[2-methyl-4-(1-oxido-4-thio morpholinyl)phenyl]-

Base Information
  • Chemical Name:Acetamide, 2-[2-(2-bromobenzoyl)-4-chlorophenoxy]-N-[2-methyl-4-(1-oxido-4-thio morpholinyl)phenyl]-
  • CAS No.:329939-33-5
  • Molecular Formula:C26H24BrClN2O4S
  • Molecular Weight:575.911
  • Hs Code.:
Acetamide,
2-[2-(2-bromobenzoyl)-4-chlorophenoxy]-N-[2-methyl-4-(1-oxido-4-thio
morpholinyl)phenyl]-

Synonyms:

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Chemical Property of Acetamide, 2-[2-(2-bromobenzoyl)-4-chlorophenoxy]-N-[2-methyl-4-(1-oxido-4-thio morpholinyl)phenyl]-
Chemical Property:
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Technology Process of Acetamide, 2-[2-(2-bromobenzoyl)-4-chlorophenoxy]-N-[2-methyl-4-(1-oxido-4-thio morpholinyl)phenyl]-

There total 8 articles about Acetamide, 2-[2-(2-bromobenzoyl)-4-chlorophenoxy]-N-[2-methyl-4-(1-oxido-4-thio morpholinyl)phenyl]- 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 benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jm050670l
Guidance literature:
Multi-step reaction with 2 steps
1.1: 3-chloroperoxybenzoic acid / CH2Cl2 / -20 - 20 °C
1.2: 4.27 g / H2 / Pd/C / ethanol; tetrahydrofuran; methanol / 3102.89 Torr
2.1: 22 percent / 1-hydroxybenzotriazole; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; Et3N / dimethylformamide / 20 °C
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm050670l
Guidance literature:
Multi-step reaction with 4 steps
1: BBr3 / CH2Cl2 / 2.08 h / -78 - 20 °C
2: K2CO3 / acetone / 4.33 h / Heating
3: 17.24 g / aq. LiOH / ethanol; tetrahydrofuran / 2.75 h / 20 °C
4: 22 percent / 1-hydroxybenzotriazole; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; Et3N / dimethylformamide / 20 °C
With lithium hydroxide; boron tribromide; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm050670l
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