methanesulfonic acid 4-{acetyl-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl ester

Base Information

Chemical Name:methanesulfonic acid 4-{acetyl-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl ester
CAS No.:862370-32-9
Molecular Formula:C₂₈H₃₇N₅O₇S
Molecular Weight:587.697
Hs Code.:

methanesulfonic acid 4-{acetyl-[2-(3-<i>tert</i>-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl ester

Synonyms:methanesulfonic acid 4-{acetyl-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl ester

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Chemical Property of methanesulfonic acid 4-{acetyl-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl ester

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Technology Process of methanesulfonic acid 4-{acetyl-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl ester

There total 2 articles about methanesulfonic acid 4-{acetyl-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl 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:

: 862370-10-3
N-(4-benzyloxy-butyl)-N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-acetamide

: 862370-32-9
methanesulfonic acid 4-{acetyl-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 36 percent / H₂ / Pd/C / ethanol / 36 h / 20 °C / 3102.89 Torr

2: N-methylmorpholine / tetrahydrofuran / 16 h / 20 °C

With 4-methyl-morpholine; hydrogen; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm0500931

Reference yield:

: 862370-16-9
N-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-N-(4-hydroxy-butyl)-acetamide

: 124-63-0
methanesulfonyl chloride

: 862370-32-9
methanesulfonic acid 4-{acetyl-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl ester

Guidance literature:: With 4-methyl-morpholine; In tetrahydrofuran; at 20 ℃; for 16h;
DOI:10.1021/jm0500931

Reference yield:

: 862370-32-9
methanesulfonic acid 4-{acetyl-[2-(3-tert-butyl-ureido)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridin-7-yl]-amino}-butyl ester

: 862369-95-7
N⁷-(4-diethylamino-butyl)-3-(3,5-dimethoxy-phenyl)-[1,6]naphthyridine-2,7-diamine

Guidance literature:: Multi-step reaction with 2 steps

1: 0.39 g / tetrahydrofuran / 96 h / 50 °C

2: 81 percent / aq. NaOH / dioxane / 144 h / 98 °C

With sodium hydroxide; In tetrahydrofuran; 1,4-dioxane;
DOI:10.1021/jm0500931