(Z)-N-(4-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide

Base Information

• Chemical Name: (Z)-N-(4-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide
• CAS No.: 1456929-07-9
• Molecular Formula: C₂₆H₂₀N₄O₇S
• Molecular Weight: 532.533

Synonyms:(Z)-N-(4-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide

Chemical Property of (Z)-N-(4-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide

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Technology Process of (Z)-N-(4-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide

There total 5 articles about (Z)-N-(4-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)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: 68.0%

N-(4-acetylphenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide (905514-05-8) + vanillin (121-33-5,8014-42-4) → (Z)-N-(4-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide (1456929-07-9)

Guidance literature:

With thionyl chloride; In ethanol; at 20 ℃; for 4h;

DOI:10.1007/s00044-013-0791-1

Reference yield:

4-(2-chloroacetamido)acetophenone (38283-38-4) → (Z)-N-(4-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide (1456929-07-9)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate / acetone / 4 h / 20 °C

2: thionyl chloride / ethanol / 4 h / 20 °C

With thionyl chloride; potassium carbonate; In ethanol; acetone;

DOI:10.1007/s00044-013-0791-1

Reference yield:

5-(3-nitrophenyl)-1,3,4-oxadiazole-2-thiol (41421-07-2) → (Z)-N-(4-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide (1456929-07-9)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate / acetone / 4 h / 20 °C

2: thionyl chloride / ethanol / 4 h / 20 °C

With thionyl chloride; potassium carbonate; In ethanol; acetone;

DOI:10.1007/s00044-013-0791-1

upstream raw materials:

3-nitrobenzoic acid hydrazide

5-(3-nitrophenyl)-1,3,4-oxadiazole-2-thiol

p-aminobenzophenone

N-(4-acetylphenyl)-2-(5-(3-nitrophenyl)-1,3,4-oxadiazol-2-ylthio)acetamide

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