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3-(6-(bis(tert-butoxycarbonyl)amino)-5-(1-(2,6-dichlorophenyl)ethoxy)pyridin-3-yl)-6-(tert-butoxycarbonyl)-5,6,7,8-tetrahydro-1,6-naphthyridin-8-ol

Base Information Edit
  • Chemical Name:3-(6-(bis(tert-butoxycarbonyl)amino)-5-(1-(2,6-dichlorophenyl)ethoxy)pyridin-3-yl)-6-(tert-butoxycarbonyl)-5,6,7,8-tetrahydro-1,6-naphthyridin-8-ol
  • CAS No.:1613148-66-5
  • Molecular Formula:C36H44Cl2N4O8
  • Molecular Weight:731.673
  • Hs Code.:
  • Mol file:1613148-66-5.mol
3-(6-(bis(tert-butoxycarbonyl)amino)-5-(1-(2,6-dichlorophenyl)ethoxy)pyridin-3-yl)-6-(tert-butoxycarbonyl)-5,6,7,8-tetrahydro-1,6-naphthyridin-8-ol

Synonyms:3-(6-(bis(tert-butoxycarbonyl)amino)-5-(1-(2,6-dichlorophenyl)ethoxy)pyridin-3-yl)-6-(tert-butoxycarbonyl)-5,6,7,8-tetrahydro-1,6-naphthyridin-8-ol

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Chemical Property of 3-(6-(bis(tert-butoxycarbonyl)amino)-5-(1-(2,6-dichlorophenyl)ethoxy)pyridin-3-yl)-6-(tert-butoxycarbonyl)-5,6,7,8-tetrahydro-1,6-naphthyridin-8-ol Edit
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Technology Process of 3-(6-(bis(tert-butoxycarbonyl)amino)-5-(1-(2,6-dichlorophenyl)ethoxy)pyridin-3-yl)-6-(tert-butoxycarbonyl)-5,6,7,8-tetrahydro-1,6-naphthyridin-8-ol

There total 12 articles about 3-(6-(bis(tert-butoxycarbonyl)amino)-5-(1-(2,6-dichlorophenyl)ethoxy)pyridin-3-yl)-6-(tert-butoxycarbonyl)-5,6,7,8-tetrahydro-1,6-naphthyridin-8-ol 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:
Guidance literature:
Multi-step reaction with 6 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 0 °C
1.2: 20 °C
2.1: iron; 3,3,5-Tribromo-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one / 1 h / 100 °C
3.1: N-Bromosuccinimide / acetonitrile / 3 h / 0 °C
4.1: dmap / N,N-dimethyl-formamide / 20 °C
5.1: potassium acetate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / dimethyl sulfoxide / 80 °C / Inert atmosphere
6.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; caesium carbonate / 1,2-dimethoxyethane; water / 95 °C / Inert atmosphere
With dmap; N-Bromosuccinimide; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate; iron; sodium hydride; caesium carbonate; 3,3,5-Tribromo-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one; In tetrahydrofuran; 1,2-dimethoxyethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile; mineral oil;
Guidance literature:
Multi-step reaction with 3 steps
1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 °C
2: trifluoroacetic acid / methanol; chloroform / 20 °C
3: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; caesium carbonate / 1,2-dimethoxyethane; water / 95 °C / Inert atmosphere
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; caesium carbonate; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In methanol; 1,2-dimethoxyethane; dichloromethane; chloroform; water;
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