4-(4-bromophenyl)-5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione

Base Information

• Chemical Name: 4-(4-bromophenyl)-5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione
• CAS No.: 1403137-49-4
• Molecular Formula: C₁₉H₁₈BrClN₄OS
• Molecular Weight: 465.801

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

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

Chemical Property:

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

There total 4 articles about 4-(4-bromophenyl)-5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-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: 80.0%

morpholine (110-91-8,99108-56-2) + formaldehyd (50-00-0,30525-89-4,61233-19-0) + 4-(4-bromophenyl)-5-(4-chlorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (537017-82-6) → 4-(4-bromophenyl)-5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (1403137-49-4)

Guidance literature:

In ethanol; at 20 ℃; for 0.5h;

DOI:10.1007/s00044-012-0248-y

Reference yield:

4-Bromophenyl isothiocyanate (1985-12-2) → 4-(4-bromophenyl)-5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (1403137-49-4)

Guidance literature:

Multi-step reaction with 3 steps

1: ethanol / 0.08 h / Reflux

2: sodium hydroxide / 2 h / Reflux

3: ethanol / 0.5 h / 20 °C

With sodium hydroxide; In ethanol;

DOI:10.1007/s00044-012-0248-y

Reference yield:

4-chlorobenzoic acid hydrazide (536-40-3) → 4-(4-bromophenyl)-5-(4-chlorophenyl)-2-(morpholin-4-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (1403137-49-4)

Guidance literature:

Multi-step reaction with 3 steps

1: ethanol / 0.08 h / Reflux

2: sodium hydroxide / 2 h / Reflux

3: ethanol / 0.5 h / 20 °C

With sodium hydroxide; In ethanol;

DOI:10.1007/s00044-012-0248-y

upstream raw materials:

morpholine

formaldehyd

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

4-Bromophenyl isothiocyanate

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