Arylation of 2‐Chloro‐3‐(4,6‐Diaryl‐1,3,5‐Triazin‐2‐yl) Quinolines: Formal Synthesis of 3‐(4,6‐Diaryl‐1,3,5‐Triazin‐2‐yl)‐2‐Substituted Quinolines by Suzuki–Miyaura Reaction

ABSTRACT We have described herein a simple and formal two‐step synthesis of 3‐(4,6‐diaryl‐1,3,5‐triazin‐2‐yl)‐2‐aryl quinolines from 2‐chloro‐3‐(4,6‐diaryl‐1,3,5‐triazin‐2‐yl) quinolines and boronic acids under the Suzuki–Miyaura conditions. This protocol provides the C‐2 arylation of 2‐chloro‐3‐(4,6‐diaryl‐1,3,5‐triazin‐2‐yl) quinolines under the mild reaction conditions. These newly formed chemo‐types may be useful in drug discovery programs or in material chemistry.

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Publication Details

Journal
Journal of Heterocyclic Chemistry
Published
2024-09-20
DOI
https://doi.org/10.1002/jhet.4909
Citations
2
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.50

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article

Arylation of 2‐Chloro‐3‐(4,6‐Diaryl‐1,3,5‐Triazin‐2‐yl) Quinolines: Formal Synthesis of 3‐(4,6‐Diaryl‐1,3,5‐Triazin‐2‐yl)‐2‐Substituted Quinolines by Suzuki–Miyaura Reaction

Mohammed B. Hawsawi, Jin‐Hee Kim, Han‐Joo Lee, Hitesh B. Jalani et al.
2 citations
Journal of Heterocyclic Chemistry
Catalytic Cross-Coupling Reactions
0.50
article

Arylation of 2‐Chloro‐3‐(4,6‐Diaryl‐1,3,5‐Triazin‐2‐yl) Quinolines: Formal Synthesis of 3‐(4,6‐Diaryl‐1,3,5‐Triazin‐2‐yl)‐2‐Substituted Quinolines by Suzuki–Miyaura Reaction

Mohammed B. Hawsawi, Jin‐Hee Kim, Han‐Joo Lee, Hitesh B. Jalani, Jin‐Hyun Jeong, Joo‐Hyun Jeon
article en
2 citations

Abstract

ABSTRACT We have described herein a simple and formal two‐step synthesis of 3‐(4,6‐diaryl‐1,3,5‐triazin‐2‐yl)‐2‐aryl quinolines from 2‐chloro‐3‐(4,6‐diaryl‐1,3,5‐triazin‐2‐yl) quinolines and boronic acids under the Suzuki–Miyaura conditions. This protocol provides the C‐2 arylation of 2‐chloro‐3‐(4,6‐diaryl‐1,3,5‐triazin‐2‐yl) quinolines under the mild reaction conditions. These newly formed chemo‐types may be useful in drug discovery programs or in material chemistry.

Journal of Heterocyclic ChemistryVol. 61(11)
Yonsei University (KR), Umm al-Qura University (SA)
Yonsei University
Good health and well-being
Openalex Percentile: Top 39%
Catalytic Cross-Coupling Reactions
0.50
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