4-(1-Isopropyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-phenyl-6-[(E)-phenylimino]-5,6-dihydro-1H-[1,3,5]triazin-2-one

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Chemical Name:4-(1-Isopropyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-phenyl-6-[(E)-phenylimino]-5,6-dihydro-1H-[1,3,5]triazin-2-one
CAS No.:199799-14-9
Molecular Formula:C₂₃H₂₁N₅O₂
Molecular Weight:399.452
Hs Code.:

Synonyms:4-(1-Isopropyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-phenyl-6-[(E)-phenylimino]-5,6-dihydro-1H-[1,3,5]triazin-2-one

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Chemical Property of 4-(1-Isopropyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-phenyl-6-[(E)-phenylimino]-5,6-dihydro-1H-[1,3,5]triazin-2-one

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Technology Process of 4-(1-Isopropyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-phenyl-6-[(E)-phenylimino]-5,6-dihydro-1H-[1,3,5]triazin-2-one

There total 7 articles about 4-(1-Isopropyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-phenyl-6-[(E)-phenylimino]-5,6-dihydro-1H-[1,3,5]triazin-2-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:

: 49609-84-9
2-Chloronicotinoyl chloride

: 199799-14-9
4-(1-Isopropyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-phenyl-6-[(E)-phenylimino]-5,6-dihydro-1H-[1,3,5]triazin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: Et₃N / Ambient temperature

2: 45 percent / NaN₃ / dimethylsulfoxide / 24 h / 90 °C

3: 99 percent / benzene / 2 h / Heating

4: 1.) C₆H₆, room temperature, overnight, 2.) reflux, 3 h

With sodium azide; triethylamine; In dimethyl sulfoxide; benzene;
DOI:10.1016/S0040-4020(97)10064-3

Reference yield:

: 14667-47-1
methyl 2-aminonicotinate

: 199799-14-9
4-(1-Isopropyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-phenyl-6-[(E)-phenylimino]-5,6-dihydro-1H-[1,3,5]triazin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / hexachloroethane, Et₃N / benzene / 3.5 h / Heating

2: 1.) C₆H₆, room temperature, overnight, 2.) reflux, 3 h

With hexachloroethane; triethylamine; In benzene;
DOI:10.1016/S0040-4020(97)10064-3

Reference yield:

: 2942-59-8
2-chloronicotinic acid

: 199799-14-9
4-(1-Isopropyl-2-oxo-1,2-dihydro-pyridin-3-yl)-1-phenyl-6-[(E)-phenylimino]-5,6-dihydro-1H-[1,3,5]triazin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: SOCl₂ / 2.5 h / Heating

2: Et₃N / Ambient temperature

3: 45 percent / NaN₃ / dimethylsulfoxide / 24 h / 90 °C

4: 99 percent / benzene / 2 h / Heating

5: 1.) C₆H₆, room temperature, overnight, 2.) reflux, 3 h

With thionyl chloride; sodium azide; triethylamine; In dimethyl sulfoxide; benzene;
DOI:10.1016/S0040-4020(97)10064-3