One-Pot Aminomethylation\nof Heteroarenes by Rongalite\nas <i>In Situ</i> C1 Source

Rongalite-mediated one-pot aminomethylation of heteroarenes\nusing\nsecondary amines/anilines has been developed. This transition-metal-free\nand mild reaction offers an efficient way to synthesize aminomethylated\nheteroaromatic compounds with high yields and broad functional group\ntolerance. Here, Rongalite plays a key role in generating the C1 unit\nsource <i>in situ</i>, which triggers the aminomethylation\nprocess. This approach provides a library of aminomethylated imidazo[1,2-<i>a</i>]pyridines and imidazo[2,1-<i>b</i>]thiazoles.

Publication Details

Journal
Figshare
Published
2024-12-04
DOI
https://doi.org/10.1021/acs.joc.4c02050.s001
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

One-Pot Aminomethylation\nof Heteroarenes by Rongalite\nas In Situ C1 Source

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Catalytic C–H Functionalization Methods
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One-Pot Aminomethylation\nof Heteroarenes by Rongalite\nas In Situ C1 Source

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Abstract

Rongalite-mediated one-pot aminomethylation of heteroarenes\nusing\nsecondary amines/anilines has been developed. This transition-metal-free\nand mild reaction offers an efficient way to synthesize aminomethylated\nheteroaromatic compounds with high yields and broad functional group\ntolerance. Here, Rongalite plays a key role in generating the C1 unit\nsource <i>in situ</i>, which triggers the aminomethylation\nprocess. This approach provides a library of aminomethylated imidazo[1,2-<i>a</i>]pyridines and imidazo[2,1-<i>b</i>]thiazoles.

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Catalytic C–H Functionalization Methods
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One-Pot Aminomethylation\nof Heteroarenes by Rongalite\nas <i>In Situ</i> C1 Source · Figshare (2024) | TGRS Research Map | TGRS