3-(2,6-difluorophenyl)-7-((5-fluoropyridin-2-yl)amino)-1-(1-methylpyrrolidin-3-yl)-1,6-naphthyridin-2(1H)-one

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Chemical Name:3-(2,6-difluorophenyl)-7-((5-fluoropyridin-2-yl)amino)-1-(1-methylpyrrolidin-3-yl)-1,6-naphthyridin-2(1H)-one
CAS No.:1588422-70-1
Molecular Formula:C₂₄H₂₀F₃N₅O
Molecular Weight:451.451
Hs Code.:

Synonyms:3-(2,6-difluorophenyl)-7-((5-fluoropyridin-2-yl)amino)-1-(1-methylpyrrolidin-3-yl)-1,6-naphthyridin-2(1H)-one

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Chemical Property of 3-(2,6-difluorophenyl)-7-((5-fluoropyridin-2-yl)amino)-1-(1-methylpyrrolidin-3-yl)-1,6-naphthyridin-2(1H)-one

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Technology Process of 3-(2,6-difluorophenyl)-7-((5-fluoropyridin-2-yl)amino)-1-(1-methylpyrrolidin-3-yl)-1,6-naphthyridin-2(1H)-one

There total 7 articles about 3-(2,6-difluorophenyl)-7-((5-fluoropyridin-2-yl)amino)-1-(1-methylpyrrolidin-3-yl)-1,6-naphthyridin-2(1H)-one 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: 16.7%

: 1588423-76-0
C₁₉H₁₆ClF₂N₃O

: 21717-96-4
2-amino-5-fluoropyridine

: 1588422-70-1
3-(2,6-difluorophenyl)-7-((5-fluoropyridin-2-yl)amino)-1-(1-methylpyrrolidin-3-yl)-1,6-naphthyridin-2(1H)-one

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium t-butanolate; XPhos; In 1,4-dioxane; at 80 ℃; for 16h; Inert atmosphere;

Reference yield:

: 40296-46-6
ethyl 4,6-dichloronicotinate

: 1588422-70-1
3-(2,6-difluorophenyl)-7-((5-fluoropyridin-2-yl)amino)-1-(1-methylpyrrolidin-3-yl)-1,6-naphthyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 72 h / 20 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / 1.5 h / -78 - 20 °C

3: manganese(IV) oxide / dichloromethane / 16 h / 20 °C

4: caesium carbonate / N,N-dimethyl-formamide / 16 h / 60 °C

5: sodium t-butanolate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere

With manganese(IV) oxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; lithium aluminium tetrahydride; caesium carbonate; N-ethyl-N,N-diisopropylamine; sodium t-butanolate; XPhos; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1588424-78-5
C₁₁H₁₆ClN₃O

: 1588422-70-1
3-(2,6-difluorophenyl)-7-((5-fluoropyridin-2-yl)amino)-1-(1-methylpyrrolidin-3-yl)-1,6-naphthyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: manganese(IV) oxide / dichloromethane / 16 h / 20 °C

2: caesium carbonate / N,N-dimethyl-formamide / 16 h / 60 °C

3: sodium t-butanolate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere

With manganese(IV) oxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate; sodium t-butanolate; XPhos; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;