(E)-7-fluoro-5-(2-(4-fluorobenzylidene)hydrazinyl)-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one

Base Information

Chemical Name:(E)-7-fluoro-5-(2-(4-fluorobenzylidene)hydrazinyl)-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one
CAS No.:1425498-35-6
Molecular Formula:C₁₉H₁₅F₂N₇O
Molecular Weight:395.371
Hs Code.:

Synonyms:(E)-7-fluoro-5-(2-(4-fluorobenzylidene)hydrazinyl)-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one

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Chemical Property of (E)-7-fluoro-5-(2-(4-fluorobenzylidene)hydrazinyl)-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one

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Technology Process of (E)-7-fluoro-5-(2-(4-fluorobenzylidene)hydrazinyl)-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one

There total 7 articles about (E)-7-fluoro-5-(2-(4-fluorobenzylidene)hydrazinyl)-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one 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: 98.0%

: 1425498-34-5
7-fluoro-5-hydrazinyl-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one

: 459-57-4
4-fluorobenzaldehyde

: 1425498-35-6
(E)-7-fluoro-5-(2-(4-fluorobenzylidene)hydrazinyl)-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one

Guidance literature:: With triethylamine; In methanol; at 29 ℃; for 12h; Inert atmosphere;

Reference yield:

: 1207453-91-5
4-amino-6-fluoroisobenzofuran-1(3H)-one

: 1425498-35-6
(E)-7-fluoro-5-(2-(4-fluorobenzylidene)hydrazinyl)-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one

Guidance literature:: Multi-step reaction with 8 steps

1.1: hydrogenchloride; hexafluorophosphoric acid; sodium nitrite / water / 4 h / -10 - 0 °C

1.2: 120 - 150 °C

2.1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane; water / 2 h / Reflux

3.1: toluene / 3 h / 100 °C / Inert atmosphere

4.1: triethylamine / dichloromethane / 3.5 h / 0 - 10 °C

5.1: 20 °C

6.1: hydrazine hydrate / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere

6.2: 60 °C

7.1: hydrogenchloride; sodium nitrite / water / 1.5 h / 0 - 5 °C / Microwave irradiation

7.2: 1 h / 0 - 5 °C

8.1: triethylamine / methanol / 12 h / 29 °C / Inert atmosphere

With hydrogenchloride; N-Bromosuccinimide; hexafluorophosphoric acid; hydrazine hydrate; triethylamine; sodium nitrite; dibenzoyl peroxide; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane; water; toluene;

Reference yield:

: 1425498-31-2
(Z)-4,6-difluoro-3-((1-methyl-1H-1,2,4-triazol-5-yl)methylene)isobenzofuran-1(3H)-one

: 1425498-35-6
(E)-7-fluoro-5-(2-(4-fluorobenzylidene)hydrazinyl)-4-((1-methyl-1H-1,2,4-triazol-5-yl)methyl)phthalazin-1(2H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: 20 °C

2.1: hydrazine hydrate / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere

2.2: 60 °C

3.1: hydrogenchloride; sodium nitrite / water / 1.5 h / 0 - 5 °C / Microwave irradiation

3.2: 1 h / 0 - 5 °C

4.1: triethylamine / methanol / 12 h / 29 °C / Inert atmosphere

With hydrogenchloride; hydrazine hydrate; triethylamine; sodium nitrite; In tetrahydrofuran; methanol; water;