16256-40-9Relevant academic research and scientific papers
IMIDAZOLINONE DERIVATIVES AS CGRP RECEPTOR ANTAGONISTS
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Page/Page column 82, (2010/08/04)
The present invention is directed to imidazolinone derivatives which are antagonists of CGRP receptors and useful in the treatment or prevention of diseases in which CGRP is involved, such as migraine. The invention is also directed to pharmaceutical comp
Glyt1 Transporter Inhibitors and Uses Thereof in Treatment of Neurological and Neuropsychiatric Disorders
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Page/Page column 28-29, (2008/12/08)
The invention provides a compound of formula (I) or a solvate thereof: wherein R1, R2, R3, R4, R5, R6, and n are as defined in the specification, and uses of such compounds. The compounds i
Zeolite-induced heterocyclization: A superior method of synthesis of imidazolidinones
Nooshabadi, Massoud A.,Aghapoor, Kioumars,Bolourtchian, Mohammad,Heravi, Majid M.
, p. 498 - 499 (2007/10/03)
A superior method for synthesis of imidazolidinones by catalytic action of H-Y zeolite from the reaction of α-aminocarboxamides with carbonyl compounds is described.
Synthesis of Novel Imidazolidinones
Khalaj,Bazaz,Shekarchi
, p. 395 - 398 (2007/10/03)
The preparation of a number of new imidazolidinones by a simple method based on the reaction of α-aminocarboxamides with carbonyl compounds is described.
Reactions of α-phenylglycinamide with some carbonyl compounds. Formation of 5,7-diisopropyl-8,8-dimethyl-2-oxo-3-phenylimidazolidino-tetrahydro--oxazine, and determination of structure and stereochemistry by nuclear Overhauser effect differenc
Qing, Ning,Colebrook, Lawrence D.,Edward, John T.,Kon, Allan,Chubb, Francis L.
, p. 1560 - 1564 (2007/10/02)
α-phenylglycinamide 5 reacts with ketones to give either the Schiff base 3 or the 4-imidazolidone 4, but reacts with boiling isobutyraldehyde to give the bicyclic compound 6.The structure and stereochemistry of 6 have been established by (1)H nuclear Over
