methyl 5-(4-(2-((tert-butoxycarbonylamino)methyl)-5-fluorophenoxy)-N-methylbutylsulfonamido)-8-methoxy-1,6-naphthyridine-7-carboxylate

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Chemical Name:methyl 5-(4-(2-((tert-butoxycarbonylamino)methyl)-5-fluorophenoxy)-N-methylbutylsulfonamido)-8-methoxy-1,6-naphthyridine-7-carboxylate
CAS No.:1292211-50-7
Molecular Formula:C₂₈H₃₅FN₄O₈S
Molecular Weight:606.672
Hs Code.:

Synonyms:methyl 5-(4-(2-((tert-butoxycarbonylamino)methyl)-5-fluorophenoxy)-N-methylbutylsulfonamido)-8-methoxy-1,6-naphthyridine-7-carboxylate

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Chemical Property of methyl 5-(4-(2-((tert-butoxycarbonylamino)methyl)-5-fluorophenoxy)-N-methylbutylsulfonamido)-8-methoxy-1,6-naphthyridine-7-carboxylate

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Technology Process of methyl 5-(4-(2-((tert-butoxycarbonylamino)methyl)-5-fluorophenoxy)-N-methylbutylsulfonamido)-8-methoxy-1,6-naphthyridine-7-carboxylate

There total 5 articles about methyl 5-(4-(2-((tert-butoxycarbonylamino)methyl)-5-fluorophenoxy)-N-methylbutylsulfonamido)-8-methoxy-1,6-naphthyridine-7-carboxylate 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: 30.0%

: 797788-35-3
methyl 5-bromo-8-methoxy-[1,6]naphthyridine-7-carboxylate

: 1292211-14-3
tert-butyl 4-fluoro-2-(4-(N-methylsulfamoyl)butoxy)benzylcarbamate

: 1292211-50-7
methyl 5-(4-(2-((tert-butoxycarbonylamino)methyl)-5-fluorophenoxy)-N-methylbutylsulfonamido)-8-methoxy-1,6-naphthyridine-7-carboxylate

Guidance literature:: With [2,2]bipyridinyl; copper(I) oxide; In 1-methyl-pyrrolidin-2-one; at 120 ℃; for 10h; Inert atmosphere;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1292211-50-7
methyl 5-(4-(2-((tert-butoxycarbonylamino)methyl)-5-fluorophenoxy)-N-methylbutylsulfonamido)-8-methoxy-1,6-naphthyridine-7-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium carbonate / 1,4-dioxane; water / 24 h / 0 - 20 °C

2: hydrogen / palladium 10% on activated carbon / ethyl acetate; ethanol / 24 h / 25 °C / 760.05 Torr

3: potassium carbonate / N,N-dimethyl-formamide / 10 h / 80 °C

4: [2,2]bipyridinyl / copper(I) oxide / 1-methyl-pyrrolidin-2-one / 10 h / 120 °C / Inert atmosphere

With [2,2]bipyridinyl; hydrogen; sodium carbonate; potassium carbonate; copper(I) oxide; palladium 10% on activated carbon; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethanol; water; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 696589-05-6
[2-(benzyloxy)-4-fluorophenyl]methanamine

: 1292211-50-7
methyl 5-(4-(2-((tert-butoxycarbonylamino)methyl)-5-fluorophenoxy)-N-methylbutylsulfonamido)-8-methoxy-1,6-naphthyridine-7-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: sodium carbonate / 1,4-dioxane; water / 24 h / 0 - 20 °C

2: hydrogen / palladium 10% on activated carbon / ethyl acetate; ethanol / 24 h / 25 °C / 760.05 Torr

3: potassium carbonate / N,N-dimethyl-formamide / 10 h / 80 °C

4: [2,2]bipyridinyl / copper(I) oxide / 1-methyl-pyrrolidin-2-one / 10 h / 120 °C / Inert atmosphere

With [2,2]bipyridinyl; hydrogen; sodium carbonate; potassium carbonate; copper(I) oxide; palladium 10% on activated carbon; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethanol; water; ethyl acetate; N,N-dimethyl-formamide;