5-(4-benzyl-1-oxo-1H-phthalazin-2-ylmethyl)-4-phenyl-1,2,4-triazol-3-thione

Base Information

Chemical Name:5-(4-benzyl-1-oxo-1H-phthalazin-2-ylmethyl)-4-phenyl-1,2,4-triazol-3-thione
CAS No.:130091-17-7
Molecular Formula:C₂₄H₁₉N₅OS
Molecular Weight:425.514
Hs Code.:

Synonyms:5-(4-benzyl-1-oxo-1H-phthalazin-2-ylmethyl)-4-phenyl-1,2,4-triazol-3-thione

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Chemical Property of 5-(4-benzyl-1-oxo-1H-phthalazin-2-ylmethyl)-4-phenyl-1,2,4-triazol-3-thione

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Technology Process of 5-(4-benzyl-1-oxo-1H-phthalazin-2-ylmethyl)-4-phenyl-1,2,4-triazol-3-thione

There total 5 articles about 5-(4-benzyl-1-oxo-1H-phthalazin-2-ylmethyl)-4-phenyl-1,2,4-triazol-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: 95.74%

: 130091-15-5
1-((4-benzyl-1-oxo-1H-phthalazin-2-yl)acetyl)-4-phenylthiosemicarbazide

: 130091-17-7
5-(4-benzyl-1-oxo-1H-phthalazin-2-ylmethyl)-4-phenyl-1,2,4-triazol-3-thione

Guidance literature:: With potassium hydroxide; In water; for 4h; Reflux;
DOI:10.1016/j.bioorg.2018.12.039

Reference yield:

: 132544-84-4
4-benzyl-1(2H)-oxophthalazin-2-acetic acid ethyl ester

: 130091-17-7
5-(4-benzyl-1-oxo-1H-phthalazin-2-ylmethyl)-4-phenyl-1,2,4-triazol-3-thione

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / N₂H₄*H₂O / ethanol / 4 h / Heating

2: 93 percent / benzene / 5 h / Heating

3: 93 percent / 2N NaOH / 2 h / Heating

With sodium hydroxide; hydrazine hydrate; In ethanol; benzene;

Reference yield:

: 130090-87-8
2-(4-benzyl-1-oxophthalazin-2(1H)-yl)acetohydrazide

: 130091-17-7
5-(4-benzyl-1-oxo-1H-phthalazin-2-ylmethyl)-4-phenyl-1,2,4-triazol-3-thione

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / benzene / 5 h / Heating

2: 93 percent / 2N NaOH / 2 h / Heating

With sodium hydroxide; In benzene;