5-Allyloxy-7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridine

Base Information

Chemical Name:5-Allyloxy-7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridine
CAS No.:1319738-18-5
Molecular Formula:C₂₀H₂₀N₂O₄
Molecular Weight:352.39
Hs Code.:

Synonyms:5-Allyloxy-7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridine

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Chemical Property of 5-Allyloxy-7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridine

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Technology Process of 5-Allyloxy-7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridine

There total 4 articles about 5-Allyloxy-7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridine 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: 86.0%

: 1319737-42-2
5-chloro-7-(3,4,5-trimethoxy-phenyl)-[1,6]-naphthyridine

: 107-18-6
allyl alcohol

: 1319738-18-5
5-Allyloxy-7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridine

Guidance literature:: allyl alcohol; With sodium hydride; In N,N-dimethyl acetamide; mineral oil; at 20 ℃; for 0.166667h; Inert atmosphere;

5-chloro-7-(3,4,5-trimethoxy-phenyl)-[1,6]-naphthyridine; In N,N-dimethyl acetamide; mineral oil; at 20 - 90 ℃;

Reference yield:

: 3222-56-8
2-methylnicotinic acid

: 1319738-18-5
5-Allyloxy-7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridine

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium diisopropyl amide / n-heptane; tetrahydrofuran; ethylbenzene / 2.17 h / -70 - 0 °C / Inert atmosphere

1.2: -73 - 20 °C / Inert atmosphere

2.1: N,N-diethylaniline; trichlorophosphate / 20 - 100 °C

3.1: sodium hydride / N,N-dimethyl acetamide; mineral oil / 0.17 h / 20 °C / Inert atmosphere

3.2: 20 - 90 °C

With sodium hydride; N,N-diethylaniline; lithium diisopropyl amide; trichlorophosphate; In tetrahydrofuran; n-heptane; N,N-dimethyl acetamide; ethylbenzene; mineral oil;

Reference yield:

: 1885-35-4
3,4,5-trimethoxybenzonitrile

: 1319738-18-5
5-Allyloxy-7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridine

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium diisopropyl amide / n-heptane; tetrahydrofuran; ethylbenzene / 2.17 h / -70 - 0 °C / Inert atmosphere

1.2: -73 - 20 °C / Inert atmosphere

2.1: N,N-diethylaniline; trichlorophosphate / 20 - 100 °C

3.1: sodium hydride / N,N-dimethyl acetamide; mineral oil / 0.17 h / 20 °C / Inert atmosphere

3.2: 20 - 90 °C

With sodium hydride; N,N-diethylaniline; lithium diisopropyl amide; trichlorophosphate; In tetrahydrofuran; n-heptane; N,N-dimethyl acetamide; ethylbenzene; mineral oil;