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2-(1-Adamantyl)-7-methylimidazo-[1,2-α]pyridine and its reactions with N-bromosuccinimide

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

In reaction with equimolar amount or twice the amount of N-bromosuccinimide 2-(1-adamantyl)-7-methylimidazo[1,2-a]pyridine, obtained from 2-amino-4-methylpyridine and bromomethyl 1-adamantyl ketone, is converted into 2-(1-adamantyl)-3-bromo-7-methylimidazo[1,2-a]pyridine. With three times the amount of N-bromosuccinimide it gives 2-(1-adamantyl)-3-bromo-7-formylimidazo[1,2-a]pyridine.

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REFERENCES

  1. R. I. Yurchenko, N. N. Svarovskaya, A. D. Ponomarenko, and A. A. Tolmachev, Khim. Geterotsikl. Soedin., 852 (2001).

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1791–1793, December, 2004.

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Yurchenko, R.I., Ponomarenko, A.D., Savina, N.S. et al. 2-(1-Adamantyl)-7-methylimidazo-[1,2-α]pyridine and its reactions with N-bromosuccinimide. Chem Heterocycl Compd 40, 1543–1545 (2004). https://doi.org/10.1007/s10593-005-0096-5

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  • DOI: https://doi.org/10.1007/s10593-005-0096-5

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