N-(2-chloro-5-(1,5-naphthyridin-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide

Base Information

Chemical Name:N-(2-chloro-5-(1,5-naphthyridin-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide
CAS No.:1201842-49-0
Molecular Formula:C₁₉H₁₂ClFN₄O₂S
Molecular Weight:414.847
Hs Code.:

Synonyms:N-(2-chloro-5-(1,5-naphthyridin-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(2-chloro-5-(1,5-naphthyridin-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide

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Technology Process of N-(2-chloro-5-(1,5-naphthyridin-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide

There total 7 articles about N-(2-chloro-5-(1,5-naphthyridin-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide 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: 57.0%

: 7689-62-5
2-chloro-1,5-naphthyridine

: 1112983-31-9
N-(2-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide

: 1201842-49-0
N-(2-chloro-5-(1,5-naphthyridin-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide

Guidance literature:: DOI:10.1021/jm200386s

Reference yield:

: 254-79-5
1,5-naphthyridine

: 1201842-49-0
N-(2-chloro-5-(1,5-naphthyridin-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 3-chloro-benzenecarboperoxoic acid / dichloromethane

2: trichlorophosphate / 8 h / 100 °C

With 3-chloro-benzenecarboperoxoic acid; trichlorophosphate; In dichloromethane; 3: Suzuki coupling;
DOI:10.1021/jm200386s

Reference yield:

: 27305-48-2
1,5-naphthyridine N-⁽¹⁾-oxide

: 1201842-49-0
N-(2-chloro-5-(1,5-naphthyridin-2-yl)pyridin-3-yl)-4-fluorobenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / 8 h / 100 °C

With trichlorophosphate; 2: Suzuki coupling;
DOI:10.1021/jm200386s