6-methyl-5-(6-trifluoromethyl-pyridin-3-yl)-4-(2,4,6-trifluoro-phenyl)-2H-pyridazin-3-one

Base Information

Chemical Name:6-methyl-5-(6-trifluoromethyl-pyridin-3-yl)-4-(2,4,6-trifluoro-phenyl)-2H-pyridazin-3-one
CAS No.:1312922-45-4
Molecular Formula:C₁₇H₉F₆N₃O
Molecular Weight:385.268
Hs Code.:

Synonyms:6-methyl-5-(6-trifluoromethyl-pyridin-3-yl)-4-(2,4,6-trifluoro-phenyl)-2H-pyridazin-3-one

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Chemical Property of 6-methyl-5-(6-trifluoromethyl-pyridin-3-yl)-4-(2,4,6-trifluoro-phenyl)-2H-pyridazin-3-one

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Technology Process of 6-methyl-5-(6-trifluoromethyl-pyridin-3-yl)-4-(2,4,6-trifluoro-phenyl)-2H-pyridazin-3-one

There total 4 articles about 6-methyl-5-(6-trifluoromethyl-pyridin-3-yl)-4-(2,4,6-trifluoro-phenyl)-2H-pyridazin-3-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:

: 1312922-44-3
5-hydroxy-5-methyl-4-(6-trifluoromethyl-pyridin-3-yl)-3-(2,4,6-trifluoro-phenyl)-5H-furan-2-one

: 1312922-45-4
6-methyl-5-(6-trifluoromethyl-pyridin-3-yl)-4-(2,4,6-trifluoro-phenyl)-2H-pyridazin-3-one

Guidance literature:: With hydrazine hydrate; In butan-1-ol; at 120 ℃; for 4h;

Reference yield:

: 597532-36-0
ethyl 6-(trifluoromethyl)nicotinate

: 1312922-45-4
6-methyl-5-(6-trifluoromethyl-pyridin-3-yl)-4-(2,4,6-trifluoro-phenyl)-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium; diisopropylamine / tetrahydrofuran; hexane / -70 °C / Inert atmosphere

1.2: -70 °C

2.1: hydrogen bromide; bromine / acetic acid / 0.5 h / 60 °C / Inert atmosphere

3.1: triethylamine / acetonitrile / 16 h / 20 °C

3.2: Cooling

3.3: 1 h

4.1: hydrazine hydrate / butan-1-ol / 4 h / 120 °C

With n-butyllithium; hydrogen bromide; bromine; hydrazine hydrate; triethylamine; diisopropylamine; In tetrahydrofuran; hexane; acetic acid; acetonitrile; butan-1-ol;

Reference yield:

: 1312922-42-1
2-methyl-3-oxo-3-(6-trifluoromethyl-pyridin-3-yl)-propionic acid tert-butyl ester

: 1312922-45-4
6-methyl-5-(6-trifluoromethyl-pyridin-3-yl)-4-(2,4,6-trifluoro-phenyl)-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen bromide; bromine / acetic acid / 0.5 h / 60 °C / Inert atmosphere

2.1: triethylamine / acetonitrile / 16 h / 20 °C

2.2: Cooling

2.3: 1 h

3.1: hydrazine hydrate / butan-1-ol / 4 h / 120 °C

With hydrogen bromide; bromine; hydrazine hydrate; triethylamine; In acetic acid; acetonitrile; butan-1-ol;