(S)-5-bromo-N-(1-(4-fluorophenyl)ethyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide

Base Information

Chemical Name:(S)-5-bromo-N-(1-(4-fluorophenyl)ethyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide
CAS No.:1223081-52-4
Molecular Formula:C₁₇H₁₃BrFN₃O₂
Molecular Weight:390.212
Hs Code.:

Synonyms:(S)-5-bromo-N-(1-(4-fluorophenyl)ethyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-5-bromo-N-(1-(4-fluorophenyl)ethyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide

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Technology Process of (S)-5-bromo-N-(1-(4-fluorophenyl)ethyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide

There total 5 articles about (S)-5-bromo-N-(1-(4-fluorophenyl)ethyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide 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: 82.0%

: 410544-37-5
5-bromo-8-hydroxy-[1,6]naphthyridine-7-carboxylic acid methyl ester

: 66399-30-2
(S)-1-(4-Fluoro-phenyl)-ethylamine

: 1223081-52-4
(S)-5-bromo-N-(1-(4-fluorophenyl)ethyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide

Guidance literature:: In toluene; for 20h; Reflux;
DOI:10.1021/jm300667v

Reference yield:

: 142777-96-6
isopropyl 3-(chlorocarbonyl)pyridine-2-carboxylate

: 1223081-52-4
(S)-5-bromo-N-(1-(4-fluorophenyl)ethyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium tetrahydroborate / tetrahydrofuran / 0 °C

2: magnesium sulfate; triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 5 h / 0 - 20 °C / Inert atmosphere

3: methanol / 3 h / 0 - 20 °C

4: N-Bromosuccinimide / dichloromethane / 1 h / 20 °C

5: toluene / 20 h / Reflux

With sodium tetrahydroborate; N-Bromosuccinimide; magnesium sulfate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; methanol; dichloromethane; toluene;
DOI:10.1021/jm300667v

Reference yield:

: 410542-68-6
8-hydroxy-1,6-naphthyridine-7-carboxylic acid methyl ester

: 1223081-52-4
(S)-5-bromo-N-(1-(4-fluorophenyl)ethyl)-8-hydroxy-1,6-naphthyridine-7-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide / dichloromethane / 1 h / 20 °C

2: toluene / 20 h / Reflux

With N-Bromosuccinimide; In dichloromethane; toluene;
DOI:10.1021/jm300667v