Acetamide, N-(4-(((3,6-dihydro-4-(5-phenyl-1,3,4-oxadiazol-2-yl)-1(2H)-pyridinyl)amino)sulfonyl)phenyl)-

Base Information

Chemical Name:Acetamide, N-(4-(((3,6-dihydro-4-(5-phenyl-1,3,4-oxadiazol-2-yl)-1(2H)-pyridinyl)amino)sulfonyl)phenyl)-
CAS No.:160857-63-6
Molecular Formula:C₂₁H₂₁N₅O₄S
Molecular Weight:439.495
Hs Code.:
DSSTox Substance ID:DTXSID30167014
Nikkaji Number:J604.871D
Wikidata:Q83036319

Synonyms:160857-63-6;Acetamide, N-(4-(((3,6-dihydro-4-(5-phenyl-1,3,4-oxadiazol-2-yl)-1(2H)-pyridinyl)amino)sulfonyl)phenyl)-;DTXSID30167014;LS-9246;N-[[1,2,3,6-Tetrahydro-4-[5-phenyl-1,3,4-oxadiazol-2-yl]pyridin]-1-yl]-4-(acetylamino)benzenesulfonamide

Suppliers and Price of Acetamide, N-(4-(((3,6-dihydro-4-(5-phenyl-1,3,4-oxadiazol-2-yl)-1(2H)-pyridinyl)amino)sulfonyl)phenyl)-

Supply Marketing:

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

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of Acetamide, N-(4-(((3,6-dihydro-4-(5-phenyl-1,3,4-oxadiazol-2-yl)-1(2H)-pyridinyl)amino)sulfonyl)phenyl)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.45g/cm³
XLogP3:1.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:6
Exact Mass:439.13142534
Heavy Atom Count:31
Complexity:754

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)NN2CCC(=CC2)C3=NN=C(O3)C4=CC=CC=C4

Technology Process of Acetamide, N-(4-(((3,6-dihydro-4-(5-phenyl-1,3,4-oxadiazol-2-yl)-1(2H)-pyridinyl)amino)sulfonyl)phenyl)-

There total 6 articles about Acetamide, N-(4-(((3,6-dihydro-4-(5-phenyl-1,3,4-oxadiazol-2-yl)-1(2H)-pyridinyl)amino)sulfonyl)phenyl)- 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:

: 160857-58-9
N-(4-{4-[1-Phenyl-meth-(E)-ylidene-hydrazinocarbonyl]-3,6-dihydro-2H-pyridin-1-ylsulfamoyl}-phenyl)-acetamide

: 160857-63-6
N-{4-[4-(5-Phenyl-[1,3,4]oxadiazol-2-yl)-3,6-dihydro-2H-pyridin-1-ylsulfamoyl]-phenyl}-acetamide

Guidance literature:: With lead dioxide; In acetic acid; for 6h; Yield given; Ambient temperature;

Reference yield:

: 100-52-7
benzaldehyde

: 160857-63-6
N-{4-[4-(5-Phenyl-[1,3,4]oxadiazol-2-yl)-3,6-dihydro-2H-pyridin-1-ylsulfamoyl]-phenyl}-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: glacid acetic acid / methanol / Heating

2: lead dioxide / acetic acid / 6 h / Ambient temperature

With lead dioxide; acetic acid; In methanol; acetic acid;

Reference yield:

: 160857-54-5
p-acetylamino-N-<4-methoxycarbonyl-1.2.5.6-tetrahydro-1-pyridyl>benzenesulphonamide

: 160857-63-6
N-{4-[4-(5-Phenyl-[1,3,4]oxadiazol-2-yl)-3,6-dihydro-2H-pyridin-1-ylsulfamoyl]-phenyl}-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 34 percent / hydrazine hydrate (99percent) / 5 h

2: glacid acetic acid / methanol / Heating

3: lead dioxide / acetic acid / 6 h / Ambient temperature

With hydrazine hydrate; lead dioxide; acetic acid; In methanol; acetic acid;