Alkyne derivatives as sphingosine 1-phosphate (s1p) receptor modulators
AssigneeAllergan, Inc.
InventorsWenkui K. Fang, Ken Chow, Evelyn G. Corpuz, Wha Bin Im
Life of this patent
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Abstract
The present invention relates to alkyne derivatives, processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals as modulators of sphingosine-1-phosphate receptors.
Claims12
A compound represented by Formula I, its enantiomers, diastereoisomers, tautomers or a pharmaceutically acceptable salt thereof,
- wherein:
- L is O, S, NH or CHR12;
- A is optionally substituted C6-10 aryl, optionally substituted heterocycle, optionally substituted C3-8 cycloalkyl or optionally substituted C5-8 cycloalkenyl;
- B is optionally substituted C8-10 aryl, optionally substituted heterocycle, optionally substituted C3-8 cycloalkyl or optionally substituted C5-8 cycloalkenyl;
- R1 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NO2, NR12R13 or hydroxyl;
- R2 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NO2, NR12R13 or hydroxyl;
- R3 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NO2, NR12R13 or hydroxyl;
- R4 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R5 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R6 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R7 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R8 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R9 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R10 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R11 is H, OH or C1-3 alkyl;
- R12 is H or C1-3 alkyl;
- and
- R13 is H or C1-3 alkyl.
The method of treating a disorder associated with sphingosine-1-phosphate receptor modulation, which comprises administering to a mammal in need thereof, a pharmaceutical composition comprising a therapeutically effective amount of at least one compound of Formula I
- wherein:
- L is O, S, NH or CHR12;
- A is optionally substituted C6-10 aryl, optionally substituted heterocycle, optionally substituted C3-8 cycloalkyl or optionally substituted C5-8 cycloalkenyl;
- B is optionally substituted C8-10 aryl, optionally substituted heterocycle, optionally substituted C3-8 cycloalkyl or optionally substituted C5-8 cycloalkenyl;
- R1 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NO2, NR12R13 or hydroxyl;
- R2 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NO2, NR12R13 or hydroxyl;
- R3 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NO2, NR12R13 or hydroxyl;
- R4 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R5 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R6 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R7 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R8 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R9 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R10 is H, halogen, —OC1-3 alkyl, optionally substituted C1-3 alkyl, CN, C(O)R11, NR12R13 or hydroxyl;
- R11 is H, OH or C1-3 alkyl;
- R12 is H or C1-3 alkyl;
- and
- R13 is H or C1-3 alkyl.
Dependencies are inferred from the claim text.