Benzamide, 5-(aminosulfonyl)-2-methoxy-N-[[4-(phenylmethyl)-2-morpholinyl]methyl]-

Base Information

• Chemical Name: Benzamide, 5-(aminosulfonyl)-2-methoxy-N-[[4-(phenylmethyl)-2-morpholinyl]methyl]-
• CAS No.: 112887-21-5
• Molecular Formula: C20H25N3O5S
• Molecular Weight: 419.502
• Mol file: 112887-21-5.mol

Synonyms:

Chemical Property of Benzamide, 5-(aminosulfonyl)-2-methoxy-N-[[4-(phenylmethyl)-2-morpholinyl]methyl]-

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of Benzamide, 5-(aminosulfonyl)-2-methoxy-N-[[4-(phenylmethyl)-2-morpholinyl]methyl]-

There total 6 articles about Benzamide, 5-(aminosulfonyl)-2-methoxy-N-[[4-(phenylmethyl)-2-morpholinyl]methyl]- 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:

4-benzyl-2-cyanomorpholine (147767-51-9,126645-52-1) → N-(4-Benzyl-morpholin-2-ylmethyl)-2-methoxy-5-sulfamoyl-benzamide (112887-21-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 1.) H₂, acetic acid / 1.) Raney nickel / 1.) 95 percent EtOH, RT, 2.) CHCl₃, RT, 2 h

2: 100 percent / 10percent HCl / 4 h / Heating

3: 1-ethyl-3-<3-(dimethylamino)propyl>carbodiimide hydrochloride / CH₂Cl₂ / 4 h / Ambient temperature

With hydrogenchloride; hydrogen; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; nickel; In dichloromethane;

DOI:10.1021/jm00167a020

Reference yield:

2-(N-acetylaminomethyl)-4-benzylmorpholine (112913-96-9) → N-(4-Benzyl-morpholin-2-ylmethyl)-2-methoxy-5-sulfamoyl-benzamide (112887-21-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 100 percent / 10percent HCl / 4 h / Heating

2: 1-ethyl-3-<3-(dimethylamino)propyl>carbodiimide hydrochloride / CH₂Cl₂ / 4 h / Ambient temperature

With hydrogenchloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane;

DOI:10.1021/jm00167a020

Reference yield:

2-(azidomethyl)-4-benzylmorpholine (112913-97-0) → N-(4-Benzyl-morpholin-2-ylmethyl)-2-methoxy-5-sulfamoyl-benzamide (112887-21-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 83 percent / sodium bis(2-methoxyethoxy)aluminum hydride / toluene / 1.5 h / Ambient temperature

2: 1-ethyl-3-<3-(dimethylamino)propyl>carbodiimide hydrochloride / CH₂Cl₂ / 4 h / Ambient temperature

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium bis(2-methoxyethoxy)aluminium dihydride; In dichloromethane; toluene;

DOI:10.1021/jm00167a020

upstream raw materials:

2-methoxy-5-sulfamoylbenzoic acid

(4-benzylmorpholin-2-yl)methanamine

4-benzyl-2-cyanomorpholine

2-(N-acetylaminomethyl)-4-benzylmorpholine

Refernces