Tricyclic compounds useful in the treatment of cancer, autoimmune and inflammatory disorders

A compound of Formula (I):

• or a pharmaceutically acceptable salt thereof, wherein:
• each is a single or double bond;
• Q is —CH2—, O, or NH;
• X is N or C;
• Y is N or C;
• Z is N or CRS;
• wherein when one of X and Y is N, the other of X and Y is C;
• RX is hydrogen or halogen;
• n is 1, 2, or 3;
• R1 is hydrogen, halogen, cyano, hydroxyl, C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C3 haloalkyl, —NRARB, or C1-C3 alkyl optionally substituted with 1-3 substituents selected from hydroxyl and C1-C3 alkoxy;
• R2 is hydrogen, halogen, amino, or C1-C3 alkyl;
• each R3 is independently deuterium, halogen, hydroxyl, C3-C6 cycloalkyl, C1-C3 alkyl, C1-C3 alkoxy, C1-C3 haloalkoxy, or C1-C3 haloalkyl;
• or two R3 together with the carbon atom to which they are attached come together to form an oxo group, a 4-8 membered heterocyclyl, or a C3-C8 cycloalkyl;
• m is 0, 1, 2, or 3;
• R4 is phenyl or 5-9 membered heteroaryl;
• wherein each R4 group is optionally substituted with 1-3 substituents independently selected from R6;
• R5 is hydrogen, halogen, cyano, hydroxyl, C1-C3 alkoxy, C1-C3 haloalkoxy, C1-C3 haloalkyl, —NRCRD, or C1-C3 alkyl;
• and
• each R6 is independently selected from halogen;
• cyano;
• amino;
• —N=(S═O)(C1-C3 alkyl)2;
• —S(═O)p(C1-C3 alkyl);
• —(C═O)NRERF;
• C1-C3 alkoxy;
• C1-C3 haloalkyl optionally substituted with hydroxyl;
• C1-C3 haloalkoxy;
• 5-6 membered heteroaryl optionally substituted with halogen, cyano, hydroxyl, C1-C3 alkoxy, C1-C3 haloalkoxy, amino, C1-C3 haloalkyl, 4-6 membered heterocyclyl, or C1-C3 alkyl optionally substituted with hydroxyl or —NRERF;
• C1-C4 alkyl optionally substituted with hydroxyl, —NRERF, or C1-C3 alkoxy;
• 3-8 membered heterocyclyl;
• and C3-C6 cycloalkoxy;
• p is 1 or 2;
• and
• RA, RB, RC, RD, RE, and RF, are independently hydrogen, C1-C3 alkyl, C3-C6 cycloalkyl, or
• RA and RB, or RC and RD, or RE and RF, together with the nitrogen atom to which they are attached come together to form a 4-6 membered heterocyclyl optionally substituted with 1-2 halogens.