Spiro-indolines for the treatment and prophylaxis of respiratory syncytial virus infection (RSV)
Benzimidazoles of formula (I): wherein: one of X and Y is an N atom or a substituted C atom, and the other is CH; L is a single bond, C 1-3 alkylene, C 2-3 alkenylene or C 2-3 alkynylene; R 1 is C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, 3- to 10-membered cycloalkyl, 5- to 10-membered heterocyclyl or 5- to 12-membered heteroaryl, each of which is unsubstituted or substituted; Z is halo, C 1-6 haloalkyl, nitro, —CN, —N(R 2 )2, —OR 2 , —SR 2 , —S(=0)R 2 , or —S(=0) 2 R 2 ; each R 2 is independently hydrogen, C 1-6 alkyl, C 2-6 alkenyl or C2-6 alkynyl, wherein said alkyl, alkenyl and alkynyl groups are unsubstituted or substituted; and m is 0 or 1; and the pharmaceutically acceptable salt thereof are inhibitors of RSV and can therefore be used to treat or prevent an RSV infection.
1. A compound which is
1′-{[5-(aminomethyl)-1-(4,4,4-trifluorobutyl)-1H-1,3-benzodiazol-2-yl]methyl}-6′-fluoro-1′,2′-dihydrospiro[cyclopropane-1,3′-indole]-2′-one;
or a pharmaceutically acceptable salt thereof.
2. A pharmaceutical composition which comprises the compound or a pharmaceutically acceptable salt thereof as defined in claim 1 and a pharmaceutically acceptable carrier or diluent.
3. A method of treating a subject suffering from or susceptible to an RSV infection, which method comprises administering to said subject an effective amount of the compound or a pharmaceutically acceptable salt thereof as defined in 1 .
4. The method of claim 3 , which includes administering one or more therapeutic agents, which is or are administered simultaneously, separately, or sequentially with the administration of the compound or a pharmaceutically acceptable salt thereof.
5. A method according to claim 4 , wherein the one or more therapeutic agents is or are selected from the group consisting of:
(i) a RSV nucleocapsid (N)-protein inhibitor;
(ii) a protein inhibitor;
(iii) an anti-RSV monoclonal antibody;
(iv) an immunomodulating toll-like receptor compound;
(v) a respiratory virus anti-viral; and
(vi) an anti-inflammatory compound.
6. A pharmaceutical composition which comprises (a) the compound or a pharmaceutically acceptable salt thereof as defined in claim 1 , and (b) one or more therapeutic agents, together with a pharmaceutically acceptable carrier or diluent.
7. A compound which is 1′-((5-(aminomethyl)-1-(tetrahydro-2H-pyran-4-yl)-1H-benzo[d]imidazol-2-yl)methyl)-6′-fluorospiro[cyclopropane-1,3′-indolin]-2′-one or a pharmaceutically acceptable salt thereof.
8. A pharmaceutical composition which comprises the compound or a pharmaceutically acceptable salt thereof as defined in claim 7 and a pharmaceutically acceptable carrier or diluent.
9. A method of treating a subject suffering from or susceptible to an RSV infection, which method comprises administering to said subject an effective amount of the compound or a pharmaceutically acceptable salt thereof as defined in claim 7 .
10. The method of claim 9 , which includes administering one or more therapeutic agents, which is or are administered simultaneously, separately, or
sequentially with the administration of the compound or a pharmaceutically acceptable salt thereof.
11. The method according to claim 10 , wherein the one or more therapeutic agents is or are selected from the group consisting of:
(i) a RSV nucleocapsid (N)-protein inhibitor;
(ii) a protein inhibitor;
(iii) an anti-RSV monoclonal antibody;
(iv) an immunomodulating toll-like receptor compound;
(v) a respiratory virus anti-viral; and
(vi) an anti-inflammatory compound.
12. A pharmaceutical composition which comprises (a) the compound a or a pharmaceutically acceptable salt thereof as defined in claim 7 , and (b) one or more therapeutic agents, together with a pharmaceutically acceptable carrier or diluent.