C1 − H morpholinomethylation and formylation of pyrrolo[1,2-a]quinoxalines

IF 1.8 3区 化学 Q3 CHEMISTRY, ORGANIC Synthetic Communications Pub Date : 2024-06-12 DOI:10.1080/00397911.2024.2361024
Thuy T. Ca , Son N. T. Phan , Tung T. Nguyen
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Abstract

We report two methods for selective morpholinomethylation and formylation of C1 − H bonds in pyrrolo[1,2-a]quinoxalines. Reaction of pyrrolo[1,2-a]quinoxalines and morpholine using CuI catalyst, (bis(trifluoroacetoxy)iodo)benzene oxidant, and DMSO solvent yielded the morpholinomethylation products. Meanwhile, formylation of C1 − H bonds in pyrrolo[1,2-a]quinoxalines progressed in the presence of CuI catalyst, trifluoroacetic acid, and DMSO solvent. Compounds bearing halogen, methylsulfonyl, pyridine, and thiophene groups were isolated in moderate yields.

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吡咯并[1,2-a]喹喔啉的 C1 - H 吗啉甲基化和甲酰化反应
我们报告了两种选择性吗啉甲基化和吡咯并[1,2-a]喹喔啉中 C1 - H 键甲酰化的方法。使用 CuI 催化剂、(双(三氟乙酰氧基)碘)苯氧化剂和 DMSO 溶剂使吡咯并[1,2-a]喹喔啉与吗啉反应,可得到吗啉甲基化产物。同时,在 CuI 催化剂、三氟乙酸和 DMSO 溶剂存在下,吡咯并[1,2-a]喹喔啉中 C1 - H 键的甲酰化反应也在进行。以中等产率分离出了带有卤素、甲磺酰基、吡啶和噻吩基团的化合物。
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来源期刊
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
期刊介绍: Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.
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