N-(3-chlorophenyl)-2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)thio)acetamide

Base Information

Chemical Name:N-(3-chlorophenyl)-2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)thio)acetamide
CAS No.:573942-41-3
Molecular Formula:C₁₅H₁₁ClN₄O₂S
Molecular Weight:346.797
Hs Code.:
DSSTox Substance ID:DTXSID601329263
ChEMBL ID:CHEMBL1720407

Synonyms:573942-41-3;N-(3-chlorophenyl)-2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)thio)acetamide;N-(3-chlorophenyl)-2-[(5-pyridin-4-yl-1,3,4-oxadiazol-2-yl)sulfanyl]acetamide;N-(3-chlorophenyl)-2-{[5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl]sulfanyl}acetamide;MLS002248445;SCHEMBL4874741;CHEMBL1720407;DTXSID601329263;HMS3083E23;STK206180;AKOS001061046;WAY-346940;SMR001315915;VU0496233-1;AB00681417-01;Z21489542;F2755-0001

Suppliers and Price of N-(3-chlorophenyl)-2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)thio)acetamide

Supply Marketing:

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

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Chemical Property of N-(3-chlorophenyl)-2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)thio)acetamide

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:346.0291245
Heavy Atom Count:23
Complexity:398

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC(=C1)Cl)NC(=O)CSC2=NN=C(O2)C3=CC=NC=C3

Technology Process of N-(3-chlorophenyl)-2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)thio)acetamide

There total 6 articles about N-(3-chlorophenyl)-2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)thio)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: 86.2%

: 573942-41-3
C₁₅H₁₁ClN₄O₂S

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 2564-05-8
2-chloro-N-(3-chlorophenyl)acetamide

: 15264-63-8
5-(4-pyridinyl)-1,3,4-oxadiazole-2-thiol

: 573942-41-3
C₁₅H₁₁ClN₄O₂S

Guidance literature:: With potassium hydroxide; In water; at 50 - 60 ℃;

Reference yield:

: 54-85-3,7640-37-1
isoniazid

: 573942-41-3
C₁₅H₁₁ClN₄O₂S

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol; water / Reflux

2: potassium hydroxide / water / 50 - 60 °C

With potassium hydroxide; sodium hydroxide; In ethanol; water;