[4-(2,5-dichlorophenoxy)pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)methanone

Base Information

Chemical Name:[4-(2,5-dichlorophenoxy)pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)methanone
CAS No.:1315468-57-5
Molecular Formula:C₂₃H₁₉Cl₂N₃O₂
Molecular Weight:440.329
Hs Code.:

Synonyms:[4-(2,5-dichlorophenoxy)pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)methanone

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Chemical Property of [4-(2,5-dichlorophenoxy)pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)methanone

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Technology Process of [4-(2,5-dichlorophenoxy)pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)methanone

There total 6 articles about [4-(2,5-dichlorophenoxy)pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)methanone 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: 72.0%

: 1315468-57-5
[4-(2,5-dichlorophenoxy)pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)methanone

Guidance literature:

Reference yield:

: 1224640-13-4
1-cyclopropyl-1,2,3,4-tetrahydro-quinoxaline

: C₁₂H₆Cl₃NO₂

: 1315468-57-5
[4-(2,5-dichlorophenoxy)pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)methanone

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1021/jm301071h

Reference yield:

: 1315469-42-1
4-(2,5-dichloro-phenoxy)-nicotinic acid

: 1315468-57-5
[4-(2,5-dichlorophenoxy)pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride / 2 h / Reflux

2: triethylamine / dichloromethane / 2 h / 20 °C

With oxalyl dichloride; triethylamine; In dichloromethane;
DOI:10.1021/jm301071h