benzhydrylidene-(5-benzotriazol-1-ylmethyl-[1,3,4]thiadiazol-2-yl)-amine

Base Information

Chemical Name:benzhydrylidene-(5-benzotriazol-1-ylmethyl-[1,3,4]thiadiazol-2-yl)-amine
CAS No.:246178-97-2
Molecular Formula:C₂₂H₁₆N₆S
Molecular Weight:396.475
Hs Code.:

Synonyms:benzhydrylidene-(5-benzotriazol-1-ylmethyl-[1,3,4]thiadiazol-2-yl)-amine

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Chemical Property of benzhydrylidene-(5-benzotriazol-1-ylmethyl-[1,3,4]thiadiazol-2-yl)-amine

Chemical Property:

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Technology Process of benzhydrylidene-(5-benzotriazol-1-ylmethyl-[1,3,4]thiadiazol-2-yl)-amine

There total 4 articles about benzhydrylidene-(5-benzotriazol-1-ylmethyl-[1,3,4]thiadiazol-2-yl)-amine 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%

: 119-61-9
benzophenone

: 246178-86-9
5-(1H-1,2,3-benzotriazol-1-ylmethyl)-1,3,4-thiadiazol-2-amine

: 246178-97-2
benzhydrylidene-(5-benzotriazol-1-ylmethyl-[1,3,4]thiadiazol-2-yl)-amine

Guidance literature:: With acetic acid; In methanol; Heating;

Reference yield:

: 95-14-7,27556-51-0
1,2,3-Benzotriazole

: 246178-97-2
benzhydrylidene-(5-benzotriazol-1-ylmethyl-[1,3,4]thiadiazol-2-yl)-amine

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / K₂CO₃ / acetone / 6 h

2: 85 percent / ethanol / Heating

3: 85 percent / conc. H₂SO₄ / 20 °C

4: 80 percent / glacial acetic acid / methanol / Heating

With sulfuric acid; potassium carbonate; acetic acid; In methanol; ethanol; acetone; 1: Substitution / 2: Substitution / 3: Cyclization / 4: Condensation;

Reference yield:

: 69218-46-8
ethyl (1H-benzotriazol-1-yl)acetate

: 246178-97-2
benzhydrylidene-(5-benzotriazol-1-ylmethyl-[1,3,4]thiadiazol-2-yl)-amine

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / ethanol / Heating

2: 85 percent / conc. H₂SO₄ / 20 °C

3: 80 percent / glacial acetic acid / methanol / Heating

With sulfuric acid; acetic acid; In methanol; ethanol; 1: Substitution / 2: Cyclization / 3: Condensation;