(R)-N-(4-cyano-2-sulfamoylphenyl)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetamide

Base Information

Chemical Name:(R)-N-(4-cyano-2-sulfamoylphenyl)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetamide
CAS No.:1269523-37-6
Molecular Formula:C₂₀H₂₀N₄O₆S
Molecular Weight:444.468
Hs Code.:

Synonyms:(R)-N-(4-cyano-2-sulfamoylphenyl)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetamide

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Chemical Property of (R)-N-(4-cyano-2-sulfamoylphenyl)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetamide

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Technology Process of (R)-N-(4-cyano-2-sulfamoylphenyl)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetamide

There total 4 articles about (R)-N-(4-cyano-2-sulfamoylphenyl)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-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:

: 240139-71-3
2-amino-5-cyanobenzenesulfonamide

: 1228773-89-4
(R)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetic acid

: 1269523-37-6
(R)-N-(4-cyano-2-sulfamoylphenyl)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetamide

Guidance literature:: 2-amino-5-cyanobenzenesulfonamide; With 1H-imidazole; thionyl chloride; In dichloromethane; at -40 - 20 ℃; for 0.5h;

(R)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetic acid; With 1,2,4-Triazole; In dichloromethane; at 0 - 25 ℃;

Reference yield:

: 1228774-07-9
(R)-tert-butyl 2-hydroxy-2-((R)-3-oxomorpholin-2-yl)acetate

: 1269523-37-6
(R)-N-(4-cyano-2-sulfamoylphenyl)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: copper(l) iodide; potassium phosphate; cis-N,N'-dimethyl-1,2-diaminocyclohexane / N,N-dimethyl-formamide / 4 h / 110 °C / Inert atmosphere

2.1: trifluoroacetic acid / dichloromethane / 1 h / 25 °C

3.1: thionyl chloride; 1H-imidazole / dichloromethane / 0.5 h / -40 - 20 °C

3.2: 0 - 25 °C

With 1H-imidazole; potassium phosphate; copper(l) iodide; thionyl chloride; cis-N,N'-dimethyl-1,2-diaminocyclohexane; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1228773-88-3
(R)-tert-butyl 2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetate

: 1269523-37-6
(R)-N-(4-cyano-2-sulfamoylphenyl)-2-hydroxy-2-((R)-3-oxo-4-(p-tolyl)morpholin-2-yl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: trifluoroacetic acid / dichloromethane / 1 h / 25 °C

2.1: thionyl chloride; 1H-imidazole / dichloromethane / 0.5 h / -40 - 20 °C

2.2: 0 - 25 °C

With 1H-imidazole; thionyl chloride; trifluoroacetic acid; In dichloromethane;