Thienopyridinone compounds and methods of treatment
View Patent ↗The invention relates to 5-HT receptor agonists and partial agonists. Novel thienopyridinone compounds represented by Formula I, and synthesis and uses thereof for treating diseases mediated directly or indirectly by 5-HT receptors, are disclosed. Such conditions include Alzheimer's disease, cognition disorders, irritable bowel syndrome, nausea, emesis, vomiting, prokinesia, gastroesophageal reflux disease, nonulcer dyspepsia, depression, anxiety, urinary incontinence, migraine, arrhythmia, atrial fibrillation, ischemic stroke, gastritis, gastric emptying disorders, feeding disorders, gastrointestinal disorders, constipation, erectile dysfunction, and respiratory depression. Methods of preparation and novel intermediates and pharmaceutical salts thereof are also included.
1. A compound having the formula
wherein
R 1 is (C 1 -C 8 ) branched or unbranched alkyl or alkenyl; a substituted or unsubstituted aryl ring, branched or unbranched haloalkyl, or a substituted or unsubstituted (CH 2 ) p -aryl, where p is 1, 2, 3, or 4;
R 2 and R 3 taken together, form a substituted or unsubstituted piperidine or pyrrolidine ring;
X is S;
Y and Z are CH;
A is NH;
E is N;
G is OH; and
n is 1, 2, 3, 4, 5 or 6; and pharmaceutically acceptable salts and/or esters thereof.
2. The compound of claim 1 , wherein R 2 and R 3 , taken together, form a pyrrolidne ring.
3. The compound of claim 1 , R 2 and R 3 , taken together, form a piperidine ring.
4. The compound of claim 1 , wherein R 1 is selected from the group consisting of methyl, ethyl, isopropyl, n-propyl, n-butyl, isobutyl, and sec-butyl, CF 3 , CH 2 CF 3 , CH(CF 3 ) 2 , and CH 2 CF 3 .
5. The compound of claim 1 , wherein n is 1, 2 or 3.
6. The compound of claim 1 , wherein n is 3.
7. The compound of claim 1 , wherein
R 1 is a (C 1 -C 8 ) alkyl or alkenyl selected from the group consisting of methyl, ethyl, isopropyl, n-propyl, allyl, n-butyl or isobutyl; and
n is 1, 2, 3, or 4.
8. The compound of claim 1 , wherein
R 1 is a (C 1 -C 8 ) alkyl or alkenyl selected from the group consisting of methyl, ethyl, isopropyl, n-propyl, allyl, n-butyl or isobutyl; and
n is 3.
9. The compound of claim 1 , wherein
R 1 is isopropyl;
R 2 and R 3 taken together form a substituted or unsubstituted piperidine (N-containing six-membered cyclic ring); and
n is 3.
10. The compound of claim 1 , wherein said pharmaceutically acceptable salt is selected from the group consisting of hydrochloride, maleate, citrate, fumarate, succinate, tartarate, mesylate, sodium, potassium, magnesium, and calcium salts.
11. The compound of claim 1 , wherein said compound is a 5-HT 4 receptor agonist.
12. The compound of claim 1 , wherein said compound is a h5-HT 4a receptor agonist.
13. The compound of claim 1 , wherein said compound is a h5-HT 4e receptor agonist.
14. A compound having the formula
wherein
R 1 is (C 1 -C 8 ) branched or unbranched alkyl; branched or unbranched haloalkyl, a substituted or unsubstituted aryl ring, or a substituted or unsubstituted (CH 2 ) p -aryl ring, where p is 1, 2, 3, or 4;
R 2 and R 3 , taken together, form a substituted or unsubstituted piperidine or pyrrolidine; and
n is 1, 2, 3, 4, 5 or 6; and pharmaceutically acceptable salts and/or esters thereof.
15. The compound of claim 14 , wherein
R 1 is a (C 1 -C 8 ) alkyl selected from the group consisting of methyl, ethyl, isopropyl, n-propyl, n-butyl or isobutyl;
R 2 and R 3 taken together form a substituted or unsubstituted piperidine (N-containing six-membered cyclic ring); and
n is 3.
16. A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.