3-(4-Methoxybenzyl)-6-phenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

Base Information

• Chemical Name: 3-(4-Methoxybenzyl)-6-phenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole
• CAS No.: 93073-22-4
• Molecular Formula: C₁₇H₁₄N₄OS
• Molecular Weight: 322.39
• DSSTox Substance ID: DTXSID50918742
• Wikidata: Q82891002
• Mol file: 93073-22-4.mol

Synonyms:93073-22-4;3-(4-methoxybenzyl)-6-phenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole;3-[(4-methoxyphenyl)methyl]-6-phenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole;5-(p-Methoxybenzyl)-2-phenyl-s-triazolo(3,4-b)-1,3,4-thiadiazole;3-((4-Methoxyphenyl)methyl)-6-phenyl-1,2,4-triazolo(3,4-b)(1,3,4)thiadiazole;1,2,4-Triazolo(3,4-b)(1,3,4)thiadiazole, 3-((4-methoxyphenyl)methyl)-6-phenyl-;C17H11N4OS;SCHEMBL12368486;DTXSID50918742;LAKSIHJCMOVJCG-UHFFFAOYSA-N;C17-H11-N4-O-S;STK320009;3-(4-methoxybenzyl)-6-phenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole;AKOS001518098;CCG-149522;LS-156933;VU0513332-1;AO-365/43356686;SR-01000917926;SR-01000917926-1;F3215-0158;3-[(4-Methoxyphenyl)methyl]-6-phenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole;methyl 4-[(6-phenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-3-yl)methyl]phenyl ether

Chemical Property of 3-(4-Methoxybenzyl)-6-phenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

Chemical Property:

• XLogP3: 3.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 322.08883226
• Heavy Atom Count: 23
• Complexity: 385

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)CC2=NN=C3N2N=C(S3)C4=CC=CC=C4

Technology Process of 3-(4-Methoxybenzyl)-6-phenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

There total 5 articles about 3-(4-Methoxybenzyl)-6-phenyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole 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: 74.0%

4-amino-3-(p-methoxybenzyl)-5-mercapto-1,2,4-triazole (93073-14-4) + benzoic acid (65-85-0,8013-63-6) → 5-(p-methoxybenzyl)-2-phenyl-s-triazolo<3,4-b>-1,3,4-thiadiazole (93073-22-4)

Guidance literature:

With trichlorophosphate; for 5h; Heating;

Reference yield: 33.0%

4-amino-3-(4-methoxybenzyl)-1H-1,2,4-triazole-5(4H)-thione (93073-14-4) + benzoic acid (65-85-0,8013-63-6) → 5-(p-methoxybenzyl)-2-phenyl-s-triazolo<3,4-b>-1,3,4-thiadiazole (93073-22-4)

Guidance literature:

With trichlorophosphate; Reflux;

DOI:10.2174/157018012799079626

Reference yield:

5-(4-methoxybenzyl)-4-amino-1,3,4-oxadiazole-2-thiol (93073-37-1) → 5-(p-methoxybenzyl)-2-phenyl-s-triazolo<3,4-b>-1,3,4-thiadiazole (93073-22-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 77 percent / hydrazine hydrate / ethanol / 12 h / Heating

2: 74 percent / POCl₃ / 5 h / Heating

With hydrazine hydrate; trichlorophosphate; In ethanol;

upstream raw materials:

4-amino-3-(p-methoxybenzyl)-5-mercapto-1,2,4-triazole

benzoic acid

5-(4-methoxybenzyl)-4-amino-1,3,4-oxadiazole-2-thiol

4-Methoxyphenylacetic acid