5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione

Base Information

• Chemical Name: 5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione
• CAS No.: 714214-94-5
• Molecular Formula: C₁₅H₁₂ClN₃OS
• Molecular Weight: 317.799

Synonyms:5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione

Chemical Property of 5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione

Chemical Property:

Purity/Quality:

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Technology Process of 5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione

There total 3 articles about 5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione 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: 89.0%

1-[(3-chlorophenyl)carbonyl]-4-(4-methoxyphenyl)thiosemicarbazide (905262-18-2) → 5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (714214-94-5)

Guidance literature:

1-[(3-chlorophenyl)carbonyl]-4-(4-methoxyphenyl)thiosemicarbazide; With sodium hydroxide; for 2h; Reflux;

With hydrogenchloride; In water;

DOI:10.1016/j.ejmech.2010.11.010

Reference yield:

3-chlorobenzhydrazide (1673-47-8) → 5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (714214-94-5)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol / 0.08 h / Reflux

2: sodium hydroxide / Reflux

With sodium hydroxide; In ethanol;

DOI:10.1016/j.ejmech.2012.11.040

Reference yield:

4-Methoxyphenyl isothiocyanate (2284-20-0) → 5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (714214-94-5)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol / 0.08 h / Reflux

2: sodium hydroxide / Reflux

With sodium hydroxide; In ethanol;

DOI:10.1016/j.ejmech.2012.11.040

upstream raw materials:

1-[(3-chlorophenyl)carbonyl]-4-(4-methoxyphenyl)thiosemicarbazide

3-chlorobenzhydrazide

4-Methoxyphenyl isothiocyanate

Downstream raw materials:

5-(3-chlorophenyl)-4-(4-methoxyphenyl)-2-(pyrrolidin-1-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione

C₃₃H₃₀ClFN₆O₄S

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