4-(4-Phenyl-1-phenylcarbamoyl-butylsulfamoyl)-thiobenzimidic acid methyl ester; hydriodide

Base Information

Chemical Name:4-(4-Phenyl-1-phenylcarbamoyl-butylsulfamoyl)-thiobenzimidic acid methyl ester; hydriodide
CAS No.:85945-82-0
Molecular Formula:C₂₅H₂₇N₃O₃S₂*HI
Molecular Weight:609.552
Hs Code.:

Synonyms:4-(4-Phenyl-1-phenylcarbamoyl-butylsulfamoyl)-thiobenzimidic acid methyl ester; hydriodide

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Chemical Property of 4-(4-Phenyl-1-phenylcarbamoyl-butylsulfamoyl)-thiobenzimidic acid methyl ester; hydriodide

Chemical Property:

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Technology Process of 4-(4-Phenyl-1-phenylcarbamoyl-butylsulfamoyl)-thiobenzimidic acid methyl ester; hydriodide

There total 6 articles about 4-(4-Phenyl-1-phenylcarbamoyl-butylsulfamoyl)-thiobenzimidic acid methyl ester; hydriodide 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: 92.0%

: 85945-70-6
5-Phenyl-2-(4-thiocarbamoyl-benzenesulfonylamino)-pentanoic acid phenylamide

: 74-88-4
methyl iodide

: 85945-82-0
4-(4-Phenyl-1-phenylcarbamoyl-butylsulfamoyl)-thiobenzimidic acid methyl ester; hydriodide

Guidance literature:: In acetone; Ambient temperature;

Reference yield:

: 34993-02-7,2046-19-7
2-(R)-amino-5-phenylpentanoic acid

: 85945-82-0
4-(4-Phenyl-1-phenylcarbamoyl-butylsulfamoyl)-thiobenzimidic acid methyl ester; hydriodide

Guidance literature:: Multi-step reaction with 5 steps

1: 45 percent / 1) 1 M NaOH; 2) HCl/H₂O / diethyl ether / 20 h / Ambient temperature

2: SOCl₂ / 1 h / Heating

3: 66 percent / benzene / 1.5 h

4: 98 percent / H₂S / pyridine; triethylamine / Ambient temperature

5: 92 percent / acetone / Ambient temperature

With hydrogenchloride; sodium hydroxide; thionyl chloride; hydrogen sulfide; water; In pyridine; diethyl ether; triethylamine; acetone; benzene;

Reference yield:

: 85945-47-7
2-(4-Cyano-benzenesulfonylamino)-5-phenyl-pentanoyl chloride

: 85945-82-0
4-(4-Phenyl-1-phenylcarbamoyl-butylsulfamoyl)-thiobenzimidic acid methyl ester; hydriodide

Guidance literature:: Multi-step reaction with 3 steps

1: 66 percent / benzene / 1.5 h

2: 98 percent / H₂S / pyridine; triethylamine / Ambient temperature

3: 92 percent / acetone / Ambient temperature

With hydrogen sulfide; In pyridine; triethylamine; acetone; benzene;