Ethyl 5-bromo-9-ethoxy-2-oxo-2H-pyrano-[2,3-g]quinoline-8-carboxylate

C D  de Oliveira; G A  Romeiro; J M S  Skakle; J L  Wardell; S M S V  Wardell

doi:10.1107/S1600536806007148

Ethyl 5-bromo-9-ethoxy-2-oxo-2H-pyrano-[2,3-g]quinoline-8-carboxylate

C D de Oliveira, G A Romeiro, J M S Skakle, J L Wardell, S M S V Wardell

Physics

Research output: Contribution to journal › Article › peer-review

2 Citations (Scopus)

Abstract

The title compound, C17H14BrNO5, was studied as part of a study on the biological properties of pyranoquinoline derivatives. Alkylation of the parent pyranoquinoline was shown to have occurred at the carbonyl rather than the amino site. The molecules are linked by a C - H (. . .) O hydrogen bond forming C(5) chains along [001].

Original language	English
Pages (from-to)	O1492-O1493
Number of pages	2
Journal	Acta Crystallographica Section E: Structure Reports Online
Volume	62
Issue number	4
DOIs	https://doi.org/10.1107/S1600536806007148
Publication status	Published - Apr 2006

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title = "Ethyl 5-bromo-9-ethoxy-2-oxo-2H-pyrano-[2,3-g]quinoline-8-carboxylate",

abstract = "The title compound, C17H14BrNO5, was studied as part of a study on the biological properties of pyranoquinoline derivatives. Alkylation of the parent pyranoquinoline was shown to have occurred at the carbonyl rather than the amino site. The molecules are linked by a C - H (. . .) O hydrogen bond forming C(5) chains along [001].",

author = "{de Oliveira}, {C D} and Romeiro, {G A} and Skakle, {J M S} and Wardell, {J L} and Wardell, {S M S V}",

year = "2006",

month = apr,

doi = "10.1107/S1600536806007148",

language = "English",

volume = "62",

pages = "O1492--O1493",

journal = "Acta Crystallographica Section E: Structure Reports Online",

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publisher = "International Union of Crystallography",

number = "4",

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T1 - Ethyl 5-bromo-9-ethoxy-2-oxo-2H-pyrano-[2,3-g]quinoline-8-carboxylate

AU - de Oliveira, C D

AU - Romeiro, G A

AU - Skakle, J M S

AU - Wardell, J L

AU - Wardell, S M S V

PY - 2006/4

Y1 - 2006/4

N2 - The title compound, C17H14BrNO5, was studied as part of a study on the biological properties of pyranoquinoline derivatives. Alkylation of the parent pyranoquinoline was shown to have occurred at the carbonyl rather than the amino site. The molecules are linked by a C - H (. . .) O hydrogen bond forming C(5) chains along [001].

AB - The title compound, C17H14BrNO5, was studied as part of a study on the biological properties of pyranoquinoline derivatives. Alkylation of the parent pyranoquinoline was shown to have occurred at the carbonyl rather than the amino site. The molecules are linked by a C - H (. . .) O hydrogen bond forming C(5) chains along [001].

U2 - 10.1107/S1600536806007148

DO - 10.1107/S1600536806007148

M3 - Article

SN - 1600-5368

VL - 62

SP - O1492-O1493

JO - Acta Crystallographica Section E: Structure Reports Online

JF - Acta Crystallographica Section E: Structure Reports Online

IS - 4

ER -

Ethyl 5-bromo-9-ethoxy-2-oxo-2H-pyrano-[2,3-g]quinoline-8-carboxylate

Abstract

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