Papd5 inhibitors and methods of use thereof

A method of treating a disease or condition selected from

• (1) a disorder associated with telomere or telomerase dysfunction;
• (2) a disorder associated with aging;
• (3) a pre-leukemic or pre-cancerous condition;
• and
• (4) neurodevelopmental disorder
• in a subject in need thereof;
• the method comprising administering to the subject in need thereof a therapeutically effective amount of a compound of Formula (I):
• or a pharmaceutically acceptable salt thereof, wherein:
• R1 is selected from O, S, N—OH, N—C1-3 alkoxy, N—NH2, and N—CN;
• W is selected from C(O)ORa1, C(O)NRc1Rd1, C(O)NRc1S(O)2Rb1, C(O)NRc1ORa1, NRc1C(O)ORa1, NRc1C(O)NRc1Rd1, NRc1C(O)Rb1, ORa1, NRc1Rd1, NRc1S(O)2Rb1, B(OH)2, P(═O)(ORa1)2, halo, CN, Cy, and a carboxylic acid bioisostere;
• or R1 and W together with the carbon atoms to which they are attached from a monocyclic 4-7 membered heterocycloalkyl ring or a monocyclic 5-6 membered heteroaryl ring, each of which is optionally substituted with 1, 2, or 3 substituents independently selected from RCy;
• X is selected from N and CR2;
• Y is selected from N and CR3;
• R2 is selected from H, Cy, halo, CN, NO2, ORa1, C1-6 alkyl, C1-6 haloalkyl, C2-6 alkenyl, and C2-6 alkynyl, wherein said C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from Cy, halo, CN, NO2, ORa1, C(O)Rb1, C(O)NRc1Rd1, C(O)ORa1, NRc1Rd1, NRc1C(O)Rb1, NRc1C(O)ORa1, NRc1S(O)2Rb1, S(O)2Rb1, and S(O)2NRc1Rd1;
• R3 is selected from H, Cy, halo, CN, NO2, ORa1, C1-6 alkyl, C1-6 haloalkyl, C2-6 alkenyl, and C2-6 alkynyl, wherein said C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from Cy, halo, CN, NO2, ORa1, C(O)Rb1, C(O)NRc1Rd1, C(O)ORa1, NRc1Rd1, NRc1C(O)Rb1, NRc1C(O)ORa1, NRc1S(O)2Rb1, S(O)2Rb1, and S(O)2NRc1Rd1.
• ring A, together with N and other atom or atoms that ring A shares with ring B, is selected from a monocyclic C3-7 cycloalkyl ring, a monocyclic 4-7 membered heterocycloalkyl ring, a phenyl ring, and a monocyclic 5-6 membered heteroaryl ring, each of which is optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from RA;
• ring B, together with the atom or atoms that ring B shares with ring A, is selected from a monocyclic C3-7 cycloalkyl ring, a monocyclic 4-7 membered heterocycloalkyl ring, a phenyl ring, and a monocyclic 5-6 membered heteroaryl ring, each of which is optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from RB;
• each RA is independently selected from H, Cy, halo, CN, NO2, ORa1, C1-6 alkyl, C1-6 haloalkyl, C2-6 alkenyl, and C2-6 alkynyl, wherein said C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from Cy, halo, CN, NO2, ORa1, C(O)Rb1, C(O)NRc1Rd1, C(O)ORa1, NRc1Rd1, NRc1C(O)Rb1, NRc1C(O)ORa1, NRc1S(O)2Rb1, S(O)2Rb1, and S(O)2NRc1Rd1;
• or any two RA groups together with the atom or atoms to which they are attached form ring C, which is selected from a monocyclic C3-7 cycloalkyl ring, a monocyclic 4-7 membered heterocycloalkyl ring, a phenyl ring, and a monocyclic 5-6 membered heteroaryl ring, each of which is optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from RC;
• each RB is independently selected from H, Cy, halo, CN, NO2, ORa1, C(O)Rb1, C(O)NRc1Rd1, C(O)ORa1, NRc1Rd1, NRc1C(O)Rb1, NRc1C(O)ORa1, NRc1S(O)2Rb1, S(O)2Rb1, S(O)2NRc1Rd1, C1-6 alkyl, C1-6 haloalkyl, C2-6 alkenyl, and C2-6 alkynyl, wherein said C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from Cy, halo, CN, NO2, ORa1, C(O)Rb1, C(O)NRc1Rd1, C(O)ORa1, NRc1Rd1, NRc1C(O)Rb1, NRc1C(O)ORa1, NRc1S(O)2Rb1, S(O)2Rb1, and S(O)2NRc1Rd1;
• or any two RB groups together with the atom or atoms to which they are attached form ring D, which is selected from a monocyclic C3-7 cycloalkyl ring, a monocyclic 4-7 membered heterocycloalkyl ring, a phenyl ring, and a monocyclic 5-6 membered heteroaryl ring, each of which is optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from RD;
• or any two RA and RB groups together with the atoms to which they are attached form a ring selected from a monocyclic C3-7 cycloalkyl ring, a monocyclic 4-7 membered heterocycloalkyl ring, and a monocyclic 5-6 membered heteroaryl ring, each of which is optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from RCy;
• each RC and RD are independently selected from H, Cy, halo, CN, NO2, ORa1, C(O)Rb1, C(O)NRc1Rd1, C(O)ORa1, NRc1Rd1, NRc1C(O)Rb1, NRc1C(O)ORa1, NRc1S(O)2Rb1, S(O)2Rb1, S(O)2NRc1Rd1, C1-6 alkyl, C1-6 haloalkyl, C2-6 alkenyl, and C2-6 alkynyl, wherein said C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from Cy, halo, CN, NO2, ORa1, C(O)Rb1, C(O)NRc1Rd1, C(O)ORa1, NRc1Rd1, NRc1C(O)Rb1, NRc1C(O)ORa1, NRc1S(O)2Rb1, S(O)2Rb1, and S(O)2NRc1Rd1;
• or any two RC groups together with the atom or atoms to which they are attached form a ring selected from a monocyclic C3-7 cycloalkyl ring, a monocyclic 4-7 membered heterocycloalkyl ring, a phenyl ring, and a monocyclic 5-6 membered heteroaryl ring, each of which is optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from RCy;
• or any two RD groups together with the atom or atoms to which they are attached form a ring selected from a monocyclic C3-7 cycloalkyl ring, a monocyclic 4-7 membered heterocycloalkyl ring, a phenyl ring, and a monocyclic 5-6 membered heteroaryl ring, each of which is optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from RCy;
• Cy is selected from C6-10 aryl, C3-10 cycloalkyl, 5-10 membered heteroaryl, and 4-10 membered heterocycloalkyl, each of which is optionally substituted with 1, 2, or 3 substituents independently selected from RCy;
• each RCy is independently selected from H, halo, CN, NO2, ORa1, C(O)Rb1, wherein said C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from halo, CN, NO2, ORa1, C(O)Rb1, C(O)NRc1Rd1, C(O)ORa1, NRc1Rd1, NRc1C(O)Rb1NRc1C(O)ORa1, NRc1S(O)2Rb1, S(O)2Rb1, and S(O)2NRc1Rd1.
• each Ra1, Rb1, Rc1, and Rd1 is independently selected from Cy1, C1-6 alkyl, C1-6 haloalkyl, C2-6 alkenyl, and C2-6 alkynyl, wherein said C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from Cy1, halo, CN, NO2, ORa2, C(O)Rb2, C(O)NRc2Rd2, C(O)ORa2, NRc2Rd2, NRc2C(O)Rb2, NRc2C(O)ORa2, NRc2S(O)2Rb2, S(O)2Rb2, and S(O)2NRc2Rd2,
• or any Rc1 and Rd1 together with the N atom to which they are attached form a 4-7 membered heterocycloalkyl, which is optionally substituted with 1, 2, or 3 substituents independently selected from Rg;
• Cy1 is selected from C6-10 aryl, C3-10 cycloalkyl, 5-10 membered heteroaryl, and 4-10 membered heterocycloalkyl, each of which is optionally substituted with 1, 2, or 3 substituents independently selected from RCy1;
• each RCy1 is independently selected from H, halo, CN, NO2, ORa2, C(O)Rb2, C(O)NRc2Rd2, C(O)ORa2, NRc2Rd2, NRc2C(O)Rb2, NRc2C(O)ORa2, NRc2S(O)2Rb2, S(O)2Rb2, S(O)2NRc2Rd2, C1-6 alkyl, C1-6 haloalkyl, C2-6 alkenyl, and C2-6 alkynyl, wherein said C1-6 alkyl, C2-6 alkenyl, and C2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from halo, CN, NO2, ORa2, C(O)Rb2, C(O)NRc2Rd2, C(O)ORa2, NRc2Rd2, NRc2C(O)Rb2, Nc2C(O)ORa2, NRc2S(O)2Rb2, S(O)2Rb2, and S(O)2NRc2Rd2,
• each Ra2, Rb2, Rc2, and Rd2 is independently selected from H, C1-6 alkyl, C1-4 haloalkyl, C2-6 alkenyl, C2-6 alkynyl, C6-10 aryl, C3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C6-10 aryl-C1-4 alkylene, C3-10 cycloalkyl-C1-4 alkylene, (5-10 membered heteroaryl)-C1-4 alkylene, and (4-10 membered heterocycloalkyl)-C1-4 alkylene, wherein said C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C6-10 aryl, C3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C6-10 aryl-C1-4 alkylene, C3-10 cycloalkyl-C1-4 alkylene, (5-10 membered heteroaryl)-C1-4 alkylene, and (4-10 membered heterocycloalkyl)-C1-4 alkylene are each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from Rg;
• or any Rc2 and Rd2 together with the N atom to which they are attached form a 4-7 membered heterocycloalkyl, which is optionally substituted with 1, 2, or 3 substituents independently selected from Rg;
• and
• each Rg is independently selected from OH, NO2, CN, halo, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-4 haloalkyl, C1-6 alkoxy, C1-6haloalkoxy, cyano-C1-3 alkylene, HO—C1-3 alkylene, C6-10 aryl, C6-10 aryloxy, C3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C6-10 aryl-C1-4 alkylene, C3-10 cycloalkyl-C1-4 alkylene, (5-10 membered heteroaryl)-C1-4alkylene, (4-10 membered heterocycloalkyl)-C1-4 alkylene, amino, C1-6 alkylamino, di(C1-6 alkyl)amino, thio, C1-6 alkylthio, C1-6 alkylsulfinyl, C1-6 alkylsulfonyl, carbamyl, C1-6 alkylcarbamyl, di(C1-6 alkyl)carbamyl, carboxy, C1-6 alkylcarbonyl, C1-6 alkoxycarbonyl, C1-6 alkylcarbonylamino, C1-6 alkylsulfonylamino, aminosulfonyl, C1-6 alkylaminosulfonyl, di(C1-6 alkyl)aminosulfonyl, aminosulfonylamino, C1-6 alkylaminosulfonylamino, di(C1-6 alkyl)aminosulfonylamino, aminocarbonylamino, C1-6 alkylaminocarbonylamino, and di(C1-6 alkyl)aminocarbonylamino.