2-(3,4-difluorophenyl)-4-(quinolin-5-ylamino)-7,8-dihydro-1,6-naphthyridin-5(6H)-one

Base Information

Chemical Name:2-(3,4-difluorophenyl)-4-(quinolin-5-ylamino)-7,8-dihydro-1,6-naphthyridin-5(6H)-one
CAS No.:1345014-94-9
Molecular Formula:C₂₃H₁₆F₂N₄O
Molecular Weight:402.403
Hs Code.:

Synonyms:2-(3,4-difluorophenyl)-4-(quinolin-5-ylamino)-7,8-dihydro-1,6-naphthyridin-5(6H)-one

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Chemical Property of 2-(3,4-difluorophenyl)-4-(quinolin-5-ylamino)-7,8-dihydro-1,6-naphthyridin-5(6H)-one

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Technology Process of 2-(3,4-difluorophenyl)-4-(quinolin-5-ylamino)-7,8-dihydro-1,6-naphthyridin-5(6H)-one

There total 9 articles about 2-(3,4-difluorophenyl)-4-(quinolin-5-ylamino)-7,8-dihydro-1,6-naphthyridin-5(6H)-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: 39.0%

: 4964-71-0
5-bromoquinoline

: 1345014-30-3
4-Amino-2-(3,4-difluorophenyl)-7,8-dihydro-1,6-naphthyridin-5(6H)-one

: 1345014-94-9
2-(3,4-difluorophenyl)-4-(quinolin-5-ylamino)-7,8-dihydro-1,6-naphthyridin-5(6H)-one

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; at 120 ℃; for 24h;
DOI:10.1016/j.tetlet.2013.06.016

Reference yield: 39.0%

: 1345014-94-9
2-(3,4-difluorophenyl)-4-(quinolin-5-ylamino)-7,8-dihydro-1,6-naphthyridin-5(6H)-one

Guidance literature:

Reference yield:

: 1345013-92-4
tert-butyl 3-[bis(methylthio)methylene]-2,4-dioxopiperidine-1-carboxylate

: 1345014-94-9
2-(3,4-difluorophenyl)-4-(quinolin-5-ylamino)-7,8-dihydro-1,6-naphthyridin-5(6H)-one

Guidance literature:: Multi-step reaction with 6 steps

1: potassium tert-butylate / dimethyl sulfoxide; tetrahydrofuran / 2 h / 25 °C

2: ammonium acetate; acetic acid / 2 h / 80 °C

3: 3-chloro-benzenecarboperoxoic acid / chloroform / 2 h / 25 °C

4: trifluoroacetic acid / chloroform / 1 h / 20 °C

5: ammonia / methanol / 4 h / 140 °C / Microwave irradiation

6: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; caesium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene / 1,4-dioxane / 24 h / 120 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium tert-butylate; ammonium acetate; ammonia; caesium carbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; methanol; chloroform; dimethyl sulfoxide;
DOI:10.1016/j.tetlet.2013.06.016