943994-29-4Relevant academic research and scientific papers
Short and efficient synthesis of oxazinone-and thiazinone-containing bicyclic heteroaromatic aldehydes
Hameed P., Shahul,Shanbhag, Gajanan,Shinde, Vikas,Chinnapattu, Murugan,Manjrekar, Praveena,Puttur, Jayashree,Patil, Vikas,Ugarkar, Bheemarao
supporting information, p. 3315 - 3321 (2013/10/01)
Short and efficient route for the synthesis of oxazinone-and thiazinone-containing bicyclic heteroaromatic aldehydes, which involves the key step of palladium-catalyzed reductive carbonylation, is described. Overall routes for the synthesis of these aldehydes are short, versatile, and scalable with good yields of the product. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]
Identification of benzoxazin-3-one derivatives as novel, potent, and selective nonsteroidal mineralocorticoid receptor antagonists
Hasui, Tomoaki,Matsunaga, Nobuyuki,Ora, Taiichi,Ohyabu, Norio,Nishigaki, Nobuhiro,Imura, Yoshimi,Igata, Yumiko,Matsui, Hideki,Motoyaji, Takashi,Tanaka, Toshimasa,Habuka, Noriyuki,Sogabe, Satoshi,Ono, Midori,Siedem, Christopher S.,Tang, Tony P.,Gauthier, Cassandra,De Meese, Lisa A.,Boyd, Steven A.,Fukumoto, Shoji
experimental part, p. 8616 - 8631 (2012/02/14)
Mineralocorticoid receptor (MR) blockade has come into focus as a promising approach for the treatment of cardiovascular diseases such as hypertension and congestive heart failure. In order to identify a novel class of nonsteroidal MR antagonists that exhibit significant potency and good selectivity over other steroidal hormone receptors, we designed a novel series of benzoxazin-3-one derivatives and synthesized them from 6-(7H-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazin-6-yl)-2H-1,4-ben-zoxazin-3(4H)-one (1a), high-throughput screening (HTS) hit compound. Our design was based on a crystal structure of an MR/compound complex and a docking model. In the course of lead generation from 1a, a 1,2-diaryl framework was characterized as a key structure with high binding affinity. On the basis of scaffold hopping and optimization studies, benzoxazin-3-one derivatives possessing 1-phenyl-3-trifluoromethylpyrazol-5-yl moiety at the 6-position were identified as a novel series of potent and selective MR antagonists. Among these compounds, 6-[1-(4-fluoro-2-methylphenyl)- 3-(trifluoromethyl)-1H-pyrazol-5-yl]-2H-1,4-benzoxazin-3(4H)-one (14n) showed highly potent activity and good selectivity and also exhibited a significant antihypertensive effect in deoxycorticosterone acetate-salt hypertensive rats. On the basis of these results, compound 14n was progressed for further pharmacological evaluation. (Figure presented)
FUSED HETEROCYCLIC COMPOUND AND USE THEREOF
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Page/Page column 296, (2008/06/13)
The present invention relates to wherein each symbol is as defined in the specification. The compound has a superior mineral corticoidreceptorantagonistic action and is useful as an agent for the prophylaxis or treatment of hypertension, cardiac failure and the like, a compound having a fused heterocycle, or a prodrug thereof, or a salt thereof; and an agent for the prophylaxis or treatment of hypertension, cardiac failure and the like.
