US2010256182A1PendingUtilityA1
Substituted 1,2,3,4-tetrahydroisoquinoline derivatives
Est. expiryMar 1, 2024(expired)· nominal 20-yr term from priority
A61P 9/10A61P 5/02A61P 9/00A61P 37/08A61P 5/06A61P 9/12A61P 3/04A61P 25/28A61P 25/18A61P 25/04A61P 3/00A61P 25/24A61P 31/00A61P 25/20A61P 25/00A61P 35/00A61P 3/10A61P 31/18A61P 25/08A61P 25/14A61P 25/16A61P 25/22A61P 15/10A61P 11/00A61P 1/06A61P 11/06A61P 15/00A61P 13/10A61P 1/00A61P 1/12A61P 19/02A61P 13/12A61P 13/08A61P 1/04A61P 1/08A61P 19/10C07D 401/06C07D 217/18C07D 217/04A61K 31/472C07D 217/24C07D 401/04
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Claims
Abstract
The invention relates to novel 1,2,3,4-tetrahydroisoquinoline derivatives of formula (I) wherein R 1 , R 2 , R 3 and X are as defined in the claims, and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and methods of treatment comprising administration of said compounds to a mammal.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 15 wherein R 1 and R 2 both represent a C 1 -C 4 alkoxy group.
3 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 2 wherein R 1 and R 2 both represent a methoxy group.
4 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 15 wherein X represents a nitrogen atom.
5 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 15 wherein X represents —CH—.
6 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 15 wherein R 3 represents a methyl group.
7 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 15 wherein R 1 and R 2 represent a methoxy group, X represents —CH— and R 3 represents C 1 -C 6 -alkyl.
8 . (canceled)
9 . (canceled)
10 . A pharmaceutical composition comprising at least one compound according to claim 15 and a pharmaceutically acceptable carrier material.
11 . (canceled)
12 . (canceled)
13 . (canceled)
14 . (canceled)
15 . A 1,2,3,4-tetrahydroisoquinoline derivative of the general formula (I)
wherein:
R 1 and R 2 independently represent hydrogen or C 1 -C 4 alkoxy;
R 3 represents C 1 -C 6 -alkyl;
X represents —CH— or a nitrogen atom;
or a pharmaceutically acceptable salt, solvent complex or morphological form, thereof.
16 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 2 wherein X represents a nitrogen atom.
17 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 2 wherein X represents —CH—.
18 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 2 wherein R 3 represents a methyl group.
19 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 3 wherein X represents a nitrogen atom.
20 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 3 wherein X represents —CH—.
21 . A 1,2,3,4-tetrahydroisoquinoline derivative according to claim 3 wherein R 3 represents a methyl group.
22 . A method of preventing or treating a disorder or disease selected from the group consisting of eating disorders or sleep disorders, comprising administering to a subject in need thereof an effective amount of the 1,2,3,4-tetrahydroisoquinoline derivative according to claim 15 .
23 . A method according to claim 22 wherein said disorder or disease is a sleep disorder.
24 . A method according to claim 23 wherein said sleep disorder is selected from the group consisting of insomnias, sleep-related dystonias, restless leg syndrome, sleep apneas, jet-lag syndrome, shift-work syndrome, delayed or advanced sleep phase syndrome.Cited by (0)
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