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- W2095687777 abstract "Potassium channel openers (KCO's) have been demonstrated to possess potent relaxant-activity on smooth muscle. Tissue-selective KCO's may find use in the treatment of a variety of diseases, such as hypertension, asthma, and urinary incontinence. We have previously reported a series of 1,9-dioxa-4-aza-phenanthrene-6-carbonitriles, including compounds 2 & 3, as bladder-selective KCO's. As a continuation of our efforts, we have designed 3-[4-acyl-2-(1-methoxy-1-methylethyl)morpholin-3-yl]-benzonitriles as ringopened analogs of compounds 2 & 3. In this report, we describe the efficient construction of the novel 2,3-disubstituted morpholine structure, as represented by the synthesis of compounds 4-7. Compounds 4-7 showed potent.and selective relaxant-activity on rat bladder detrusor strip preparation. In this series, the most potent derivatives are Boc-substituted analogs 4 & 6 (IC 5 0 = 3.9 and 2.9 μM, respectively)." @default.
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- W2095687777 date "2004-02-01" @default.
- W2095687777 modified "2023-10-14" @default.
- W2095687777 title "Synthesis of 3-[4-Acyl-2-(1-methoxy-1-methylethyl)morpholin-3-yl]-benzonitriles as Novel Potassium Channel Openers" @default.
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- W2095687777 doi "https://doi.org/10.1002/jccs.200400024" @default.
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