N-[4-(3-morpholin-4-ylpropylsulfamoyl)phenyl]acetamide

Base Information

Chemical Name:N-[4-(3-morpholin-4-ylpropylsulfamoyl)phenyl]acetamide
CAS No.:77283-38-6
Molecular Formula:C₁₅H₂₃N₃O₄S
Molecular Weight:341.431
Hs Code.:
DSSTox Substance ID:DTXSID901320739
ChEMBL ID:CHEMBL1864603

Synonyms:77283-38-6;N-[4-(3-morpholin-4-ylpropylsulfamoyl)phenyl]acetamide;N-[4-(3-Morpholin-4-yl-propylsulfamoyl)-phenyl]-acetamide;N-(4-{[3-(morpholin-4-yl)propyl]sulfamoyl}phenyl)acetamide;MLS001229556;SCHEMBL9885410;CHEMBL1864603;DTXSID901320739;HMS2903G23;STK723438;AKOS000602824;SMR000612571;AE-848/36304055;4-acetamido-N-(3-morpholinopropyl)benzenesulphonamide;F1677-0425;N-(4-(N-(3-morpholinopropyl)sulfamoyl)phenyl)acetamide;Acetamide, N-[4-(3-morpholin-4-ylpropylsulfamoyl)phenyl]-;N~1~-(4-{[(3-morpholinopropyl)amino]sulfonyl}phenyl)acetamide;N-[4-({[3-(4-morpholinyl)propyl]amino}sulfonyl)phenyl]acetamide

Suppliers and Price of N-[4-(3-morpholin-4-ylpropylsulfamoyl)phenyl]acetamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-[4-(3-morpholin-4-ylpropylsulfamoyl)phenyl]acetamide

Chemical Property:

XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:7
Exact Mass:341.14092740
Heavy Atom Count:23
Complexity:464

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC=C(C=C1)S(=O)(=O)NCCCN2CCOCC2

Technology Process of N-[4-(3-morpholin-4-ylpropylsulfamoyl)phenyl]acetamide

There total 2 articles about N-[4-(3-morpholin-4-ylpropylsulfamoyl)phenyl]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: 62.0%

: 123-00-2
4-(3-Aminopropyl)morpholine

: 121-60-8
p-acetylaminobenzenesulfonyl chloride

: 77283-38-6
N-acetyl-sulfanilic acid-(3-morpholino-propylamide)

Guidance literature:: With potassium carbonate; In acetone; at 20 ℃; for 2.25h;

Reference yield:

: 4542-47-6
3-Morpholin-4-yl-propionitrile

: 77283-38-6
N-acetyl-sulfanilic acid-(3-morpholino-propylamide)

Guidance literature:: Multi-step reaction with 2 steps

1: ethanolic NH₃ / 105 °C / 147102 - 205942 Torr

2: K₂CO₃; aqueous acetone

With ammonia; potassium carbonate; acetone;
DOI:10.1021/ja01233a019