N-(3-benzyloxy-propyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide

Base Information

Chemical Name:N-(3-benzyloxy-propyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide
CAS No.:862370-09-0
Molecular Formula:C₃₃H₃₉N₅O₅
Molecular Weight:585.703
Hs Code.:

<i>N</i>-(3-benzyloxy-propyl)-<i>N</i>-[2-(3-<i>tert</i>-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide

Synonyms:N-(3-benzyloxy-propyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide

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Chemical Property of N-(3-benzyloxy-propyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide

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Technology Process of N-(3-benzyloxy-propyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide

There total 4 articles about N-(3-benzyloxy-propyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide 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: 75.0%

: 5375-00-8
3-benzyloxypropyl iodide

: 311819-90-6
N-[2-[[(tert-butylamino)carbonyl]amino]-3-(3,5-dimethoxyphenyl)-1,6-naphthyridin-7-yl]acetamide

: 862370-12-5
1-[7-(3-benzyloxy-propylamino)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-2-yl]-3-tert-butyl-urea

: 862370-09-0
N-(3-benzyloxy-propyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide

Guidance literature:: N-[2-[[(tert-butylamino)carbonyl]amino]-3-(3,5-dimethoxyphenyl)-1,6-naphthyridin-7-yl]acetamide; With sodium hydride; In N,N-dimethyl-formamide; for 1.66667h;

3-benzyloxypropyl iodide; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 24h;
DOI:10.1021/jm0500931

Reference yield: 23.0%

: 862370-12-5
1-[7-(3-benzyloxy-propylamino)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-2-yl]-3-tert-butyl-urea

: 75-36-5
acetyl chloride

: 862370-09-0
N-(3-benzyloxy-propyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide

: N-[2-(1-acetyl-3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-N-(3-benzyloxy-propyl)-acetamide

Guidance literature:: With 4-methyl-morpholine; In tetrahydrofuran; at 20 ℃; for 21h;
DOI:10.1021/jm0500931

Reference yield:

: 4799-68-2
3-benzyloxypropan-1-ol

: 862370-09-0
N-(3-benzyloxy-propyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 72 percent / PPh₃; imidazole; iodine / benzene / 0.83 h / Heating

2.1: NaH / dimethylformamide / 1.67 h

2.2: 75 percent / dimethylformamide / 24 h / 0 - 20 °C

With 1H-imidazole; iodine; sodium hydride; triphenylphosphine; In N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm0500931