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6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one.


ABSTRACT: The title compound, C(7)H(6)BrN(3)O, was obtained from the reaction of 6-bromo-1H-imidazo[4,5-b]pyridin-2(3H)-one with methyl iodide. All non-H atoms lie in a common plane [r.m.s deviation = 0.017?(1)?Å]. The amino group is a hydrogen-bond donor to the carbonyl group of an inversion-related mol-ecule, the pair of hydrogen bonds giving rise to a hydrogen-bonded dimer.

SUBMITTER: Ghacham HB 

PROVIDER: S-EPMC2979211 | biostudies-literature | 2010 Apr

REPOSITORIES: biostudies-literature

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6-Bromo-3-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one.

Ghacham Hend Bel HB   Rodi Youssef Kandri YK   Capet Frédéric F   Essassi El Mokhtar el M   Ng Seik Weng SW  

Acta crystallographica. Section E, Structure reports online 20100414 Pt 5


The title compound, C(7)H(6)BrN(3)O, was obtained from the reaction of 6-bromo-1H-imidazo[4,5-b]pyridin-2(3H)-one with methyl iodide. All non-H atoms lie in a common plane [r.m.s deviation = 0.017 (1) Å]. The amino group is a hydrogen-bond donor to the carbonyl group of an inversion-related mol-ecule, the pair of hydrogen bonds giving rise to a hydrogen-bonded dimer. ...[more]

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