(Z)-2,3,4,5-tetrafluoro-N-(7-p-tolyl-4H-pyrazolo[5,1-d][1,2,3,5]thiatriazin-4-ylidene)-benzamide

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Chemical Name:(Z)-2,3,4,5-tetrafluoro-N-(7-p-tolyl-4H-pyrazolo[5,1-d][1,2,3,5]thiatriazin-4-ylidene)-benzamide
CAS No.:1448041-59-5
Molecular Formula:C₁₈H₉F₄N₅OS
Molecular Weight:419.362
Hs Code.:

Synonyms:(Z)-2,3,4,5-tetrafluoro-N-(7-p-tolyl-4H-pyrazolo[5,1-d][1,2,3,5]thiatriazin-4-ylidene)-benzamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (Z)-2,3,4,5-tetrafluoro-N-(7-p-tolyl-4H-pyrazolo[5,1-d][1,2,3,5]thiatriazin-4-ylidene)-benzamide

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Technology Process of (Z)-2,3,4,5-tetrafluoro-N-(7-p-tolyl-4H-pyrazolo[5,1-d][1,2,3,5]thiatriazin-4-ylidene)-benzamide

There total 2 articles about (Z)-2,3,4,5-tetrafluoro-N-(7-p-tolyl-4H-pyrazolo[5,1-d][1,2,3,5]thiatriazin-4-ylidene)-benzamide 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: 83.0%

: 950725-15-2
2,3,4,5-tetrafluorobenzoyl isothiocyanate

: 144993-01-1
3-diazo-5-(p-tolyl)-3H-pyrazole

: 1448041-59-5
(Z)-2,3,4,5-tetrafluoro-N-(7-p-tolyl-4H-pyrazolo[5,1-d][1,2,3,5]thiatriazin-4-ylidene)-benzamide

Guidance literature:: In ethyl acetate; at -10 - 20 ℃; Darkness;
DOI:10.1016/j.tet.2013.06.062

Reference yield:

: 151293-15-1
5-amino-3-(4-methylphenyl)-1H-pyrazole

: 1448041-59-5
(Z)-2,3,4,5-tetrafluoro-N-(7-p-tolyl-4H-pyrazolo[5,1-d][1,2,3,5]thiatriazin-4-ylidene)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium nitrite; hydrogenchloride / -5 °C

2: ethyl acetate / -10 - 20 °C / Darkness

With hydrogenchloride; sodium nitrite; In ethyl acetate;
DOI:10.1016/j.tet.2013.06.062