3-bromomethyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester

Base Information

Chemical Name:3-bromomethyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester
CAS No.:1418026-04-6
Molecular Formula:C₁₈H₁₂BrF₃N₂O₃
Molecular Weight:441.204
Hs Code.:

Synonyms:3-bromomethyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester

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Chemical Property of 3-bromomethyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester

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Technology Process of 3-bromomethyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester

There total 7 articles about 3-bromomethyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester 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:

: 1418026-03-5
3-methyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester

: 1418026-04-6
3-bromomethyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester

Guidance literature:: With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 2h; under 760.051 Torr; Inert atmosphere; Reflux;

Reference yield:

: 62-53-3
aniline

: 1418026-04-6
3-bromomethyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 2 h / -78 °C / 760.05 Torr / Inert atmosphere

1.2: -78 - 20 °C / 760.05 Torr / Inert atmosphere

1.3: 760.05 Torr / Inert atmosphere

2.1: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 4 h / 25 °C / 760.05 Torr / Inert atmosphere

3.1: tetrahydrofuran / 4.5 h / 0 - 20 °C / 760.05 Torr / Inert atmosphere

4.1: toluene / 18 h / 760.05 Torr / Inert atmosphere; Reflux

5.1: potassium carbonate / methanol / 2 h / 760.05 Torr / Inert atmosphere; Reflux

6.1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 2 h / 760.05 Torr / Inert atmosphere; Reflux

With N-Bromosuccinimide; potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; dibenzoyl peroxide; In tetrahydrofuran; methanol; tetrachloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1402345-24-7
2-phenylamino-6-trifluoromethyl-nicotinic acid

: 1418026-04-6
3-bromomethyl-4-oxo-1-phenyl-7-trifluoromethyl-1,4-dihydro-[1,8]naphthyridine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 4 h / 25 °C / 760.05 Torr / Inert atmosphere

2: tetrahydrofuran / 4.5 h / 0 - 20 °C / 760.05 Torr / Inert atmosphere

3: toluene / 18 h / 760.05 Torr / Inert atmosphere; Reflux

4: potassium carbonate / methanol / 2 h / 760.05 Torr / Inert atmosphere; Reflux

5: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 2 h / 760.05 Torr / Inert atmosphere; Reflux

With N-Bromosuccinimide; potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; dibenzoyl peroxide; In tetrahydrofuran; methanol; tetrachloromethane; N,N-dimethyl-formamide; toluene;