Acetamide, N-(4-(aminosulfonyl)phenyl)-2-(benzoylamino)-

Base Information

Chemical Name:Acetamide, N-(4-(aminosulfonyl)phenyl)-2-(benzoylamino)-
CAS No.:63203-12-3
Molecular Formula:C₁₅H₁₅N₃O₄S
Molecular Weight:333.368
Hs Code.:
DSSTox Substance ID:DTXSID20212567
Wikidata:Q83087708

Synonyms:BRN 2775891;Acetamide, N-(4-(aminosulfonyl)phenyl)-2-(benzoylamino)-;63203-12-3;N-(4-(Aminosulfonyl)phenyl)-2-(benzoylamino)acetamide;4-14-00-02756 (Beilstein Handbook Reference);LS-8101;C15H15N3O4S;DTXSID20212567;C15-H15-N3-O4-S

Suppliers and Price of Acetamide, N-(4-(aminosulfonyl)phenyl)-2-(benzoylamino)-

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 1 raw suppliers

Chemical Property of Acetamide, N-(4-(aminosulfonyl)phenyl)-2-(benzoylamino)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.411g/cm³
XLogP3:0.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:333.07832714
Heavy Atom Count:23
Complexity:515

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NCC(=O)NC2=CC=C(C=C2)S(=O)(=O)N

Technology Process of Acetamide, N-(4-(aminosulfonyl)phenyl)-2-(benzoylamino)-

There total 6 articles about Acetamide, N-(4-(aminosulfonyl)phenyl)-2-(benzoylamino)- 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: 36.0%

: 133639-71-1
2-amino-N-(4-sulfamoylphenyl)acetamide

: 98-88-4
benzoyl chloride

: 63203-12-3
N-(2-oxo-2-((4-sulfamoylphenyl)amino)ethyl)benzamide

Guidance literature:: In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 1h;
DOI:10.1002/cmdc.202100510

Reference yield:

: 495-69-2,140480-84-8,21251-67-2,91787-63-2,66407-11-2
Hippuric Acid

: 63203-12-3
N-(2-oxo-2-((4-sulfamoylphenyl)amino)ethyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 0.33 h / -7 - -5 °C

2: tetrahydrofuran / 3 h / Ambient temperature

With triethylamine; In tetrahydrofuran;
DOI:10.1007/BF00777266

Reference yield:

: 63-74-1
sulfanilamide

: 63203-12-3
N-(2-oxo-2-((4-sulfamoylphenyl)amino)ethyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 0 °C

1.2: 20 °C

2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 0.33 h / 20 °C

3.1: N,N-dimethyl-formamide; dichloromethane / 1 h / 20 °C

With 1,8-diazabicyclo[5.4.0]undec-7-ene; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/cmdc.202100510