INHIBITORS OF RAF KINASES

1 - 68 . (canceled)

69 . A compound, or pharmaceutically acceptable salt or solvate thereof, having the structure of Formula (V):

(V)

wherein,

ring A is a 5- or 6-membered optionally substituted heteroaryl, or 5- or 6-membered optionally substituted heterocyclyl;

W is NH, or NR7;

X is N, C—H, C—F, or C—CN;

Y is N, C—F, or C—H;

R is H, C1-C8 optionally substituted alkyl, (C1-C8 optionally substituted alkylene)-OPO(OH) 2 , C3-C6 optionally substituted cycloalkyl, (C3-C6 optionally substituted cycloalkylene)-OPO(OH) 2 , C4-C8 optionally substituted cycloalkylalkyl, (C3-C6 optionally substituted cycloalkylalkylene)-OPO(OH) 2 , C3-C6 optionally substituted heterocyclyl, (C3-C6 optionally substituted heterocyclyl)-OPO(OH) 2 , C3-C6 optionally substituted heterocyclylalkyl, (C3-C6 optionally substituted heterocyclylalkyl)-OPO(OH)2, C1-C8 optionally substituted alkyl-CO—, SO2—(C1-C8 optionally substituted alkyl), —SO2—(C3-C6 optionally substituted cycloalkyl), —SO2—(C4-C8 optionally substituted cycloalkylalkyl), —SO2—(C3-C6 optionally substituted heterocyclyl), —SO2—(C3-C6 optionally substituted heterocyclylalkyl), —SO2-N(R8)R9-C1-C8 optionally substituted alkyl, -C02-C1-C8 optionally substituted alkyl, or —CO—N(R8)R9-C1-C8 optionally substituted alkyl;

each R8 and R9 is independently selected from H or C1-C8 optionally substituted alkyl;

R2 is H, D or F;

R4 is halogen, optionally substituted C1-C3 alkyl, -CD3, or optionally substituted C1-C3 alkoxy;

R6 is H, D, Cl or F;

R7 is C1-C8 optionally substituted alkyl; or R is not H, and R and R7 optionally join to form an optionally substituted heterocyclyl ring;

Z is (a) wherein m is 0, 1, 2, or 3; p is 0, 1, 2, 3, or 4; and each R11 is independently selected from amino, alkylamino, dialkylamino, —OH, halogen, optionally substituted C1-C6 alkyl, optionally substituted C3-C6 cycloalkyl, optionally substituted C1-C6 alkoxy, optionally substituted C2-C6 alkynyl, optionally substituted —S-alkyl, optionally substituted —SO2alkyl, optionally substituted C3-C6 cycloalkylalkyl, optionally substituted heterocyclyl, or optionally substituted heterocyclylalkyl; or two RI 1 groups together form an oxo; or

(b) wherein m is 0, 1, 2, or 3; n is 0, 1, 2, or 3; p is 0, 1, 2, 3, or 4; and each R11 is independently selected from amino, alkylamino, dialkylamino, —OH, halogen, optionally substituted C1-C6 alkyl, optionally substituted C3-C6 cycloalkyl, optionally substituted C1-C6 alkoxy, optionally substituted C2-C6 alkynyl, optionally substituted —S-alkyl, optionally substituted —SO2alkyl, optionally substituted C3-C6 cycloalkylalkyl, optionally substituted heterocyclyl, or optionally substituted heterocyclylalkyl; or two RI 1 groups together form an oxo.

70 . The compound of claim 69 , or pharmaceutically acceptable salt or solvate thereof, wherein ring A is a 5- or 6-membered optionally substituted heteroaryl.

71 . The compound of claim 69 , or pharmaceutically acceptable salt or solvate thereof, wherein ring A is an optionally substituted morpholine.

72 . The compound of claim 69 , or pharmaceutically acceptable salt or solvate thereof, wherein W is NH.

73 . The compound of claim 69 , or pharmaceutically acceptable salt or solvate thereof, wherein W is NR7.

74 . The compound of claim 69 , or pharmaceutically acceptable salt or solvate thereof, wherein W is NR7, R is not H, and R and R7 join to form an optionally substituted heterocyclyl ring.

75 . The compound of claim 69 , or pharmaceutically acceptable salt or solvate thereof wherein R is SO2—(C1-C8 optionally substituted alkyl), —SO2—(C3-C6 optionally substituted cycloalkyl), —SO2—(C4-C8 optionally substituted cycloalkylalkyl), —SO2—(C3-C6 optionally substituted heterocyclyl), —SO2—(C3-C6 optionally substituted heterocyclylalkyl), —SO2—N(R8)R9-C1-C8 optionally substituted alkyl, —CO2-C1-C8 optionally substituted alkyl, or —CO—N(R8)R9-C1-C8 optionally substituted alkyl;

each R8 and R9 is independently selected from H or C1-C8 optionally substituted alkyl.

76 . The compound of claim 69 , or pharmaceutically acceptable salt or solvate thereof wherein R is C1-C8 optionally substituted alkylene)-OPO(OH) 2 , C3-C6 optionally substituted cycloalkyl, (C3-C6 optionally substituted cycloalkylene)-OPO(OH) 2 , C4-C8 optionally substituted cycloalkylalkyl, (C3-C6 optionally substituted cycloalkylalkylene)-OPO(OH) 2 , C3-C6 optionally substituted heterocyclyl, (C3-C6 optionally substituted heterocyclyl)-OPO(OH) 2 , C3-C6 optionally substituted heterocyclylalkyl, (C3-C6 optionally substituted heterocyclylalkyl)-OPO(OH) 2 , C1-C8 optionally substituted alkyl-CO—.

77 . A pharmaceutical composition comprising a compound of formula (V) or a pharmaceutically acceptable salt or solvate thereof as described in claim 69 and a pharmaceutically acceptable excipient.

78 . The pharmaceutical composition of claim 77 formulated for oral administration or for administration by injection.

79 . A method of preparing a pharmaceutical composition comprising mixing a compound, or pharmaceutically acceptable salt or solvate thereof, of claim 69 , and a pharmaceutically acceptable carrier.

80 . A method of treating cancer in a patient in need thereof comprising administering to the patient a compound of Formula (V), or a pharmaceutically acceptable salt or solvate thereof as described in claim 69 .

81 . A method of treating cancer in a patient in need thereof comprising administering to the patient a pharmaceutical composition as described in claim 77 .

82 . The method of treating cancer of claim 81 wherein the pharmaceutical composition is administered orally or by injection.

83 . The method of treating cancer of claim 81 wherein the pharmaceutical composition is administered orally and wherein the oral dose ranges from 1.0 mg to about 1000 mg, one to four times or more, per day.