4-[3,5-bis(trifluoromethyl)benzyl]-6-(2-methylphenyl)-5-oxo-2,3,4,5-tetrahydropyrido[3,2-f] [1,4]oxazepine

Base Information

Chemical Name:4-[3,5-bis(trifluoromethyl)benzyl]-6-(2-methylphenyl)-5-oxo-2,3,4,5-tetrahydropyrido[3,2-f] [1,4]oxazepine
CAS No.:544671-99-0
Molecular Formula:C₂₄H₁₈F₆N₂O₂
Molecular Weight:480.41
Hs Code.:

Synonyms:4-[3,5-bis(trifluoromethyl)benzyl]-6-(2-methylphenyl)-5-oxo-2,3,4,5-tetrahydropyrido[3,2-f] [1,4]oxazepine

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Chemical Property of 4-[3,5-bis(trifluoromethyl)benzyl]-6-(2-methylphenyl)-5-oxo-2,3,4,5-tetrahydropyrido[3,2-f] [1,4]oxazepine

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Technology Process of 4-[3,5-bis(trifluoromethyl)benzyl]-6-(2-methylphenyl)-5-oxo-2,3,4,5-tetrahydropyrido[3,2-f] [1,4]oxazepine

There total 4 articles about 4-[3,5-bis(trifluoromethyl)benzyl]-6-(2-methylphenyl)-5-oxo-2,3,4,5-tetrahydropyrido[3,2-f] [1,4]oxazepine 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:

: C₂₄H₁₉ClF₆N₂O₂

: 544671-99-0
4-[3,5-bis(trifluoromethyl)benzyl]-6-(2-methylphenyl)-5-oxo-2,3,4,5-tetrahydropyrido[3,2-f] [1,4]oxazepine

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 0 - 20 ℃; for 2h;

Reference yield:

: 544671-98-9
2-chloro-4-(2-methylphenyl)nicotinic acid

: 544671-99-0
4-[3,5-bis(trifluoromethyl)benzyl]-6-(2-methylphenyl)-5-oxo-2,3,4,5-tetrahydropyrido[3,2-f] [1,4]oxazepine

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride; N,N-dimethyl-formamide / 1 h / Heating / reflux

2: triethylamine / tetrahydrofuran / 2 h / 0 - 20 °C

3: potassium tert-butylate / tetrahydrofuran / 2 h / 0 - 20 °C

With thionyl chloride; potassium tert-butylate; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran;

Reference yield:

: 544671-98-9
2-chloro-4-(2-methylphenyl)nicotinic acid

: 156241-24-6
2-[[3,5-bis(trifluoromethyl)benzyl]amino]-1-ethanol

: 544671-99-0
4-[3,5-bis(trifluoromethyl)benzyl]-6-(2-methylphenyl)-5-oxo-2,3,4,5-tetrahydropyrido[3,2-f] [1,4]oxazepine

Guidance literature:: Multi-step reaction with 2 steps

1.1: thionyl chloride; N,N-dimethyl-formamide / 1 h / Heating / reflux

1.2: 2 h / 0 - 20 °C

2.1: potassium tert-butylate / tetrahydrofuran / 2 h / 0 - 20 °C

With thionyl chloride; potassium tert-butylate; N,N-dimethyl-formamide; In tetrahydrofuran;