EP4384160A1 - Composés hétérocycliques et procédés d'utilisation - Google Patents

Composés hétérocycliques et procédés d'utilisation

Info

Publication number
EP4384160A1
EP4384160A1 EP22856568.5A EP22856568A EP4384160A1 EP 4384160 A1 EP4384160 A1 EP 4384160A1 EP 22856568 A EP22856568 A EP 22856568A EP 4384160 A1 EP4384160 A1 EP 4384160A1
Authority
EP
European Patent Office
Prior art keywords
fluoro
methoxy
pyrimidin
pyrido
pyrrolizin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP22856568.5A
Other languages
German (de)
English (en)
Inventor
Michael M. YAMANO
Yunxiao Li
Primali NAVARATNE
Jose Medina
Ning Chen
Liping Pettus
Rene Rahimoff
Xiaofen Li
John Stellwagen
Francesco Manoni
Kexue Li
Brian Alan Lanman
Ryan Paul Wurz
Wei Zhao
Huan RUI
Josephine ESHON
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Amgen Inc
Original Assignee
Amgen Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Amgen Inc filed Critical Amgen Inc
Publication of EP4384160A1 publication Critical patent/EP4384160A1/fr
Pending legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Definitions

  • HETEROCYCLIC COMPOUNDS AND METHODS OF USE CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Patent Application No. 63/231,543, filed August 10, 2021 and U.S. Provisional Patent Application No. 63/289,579, filed December 14, 2021, each of which is incorporated by reference in its entirety.
  • FIELD The present disclosure provides compounds having activity as inhibitors of G12D mutant KRAS protein.
  • This disclosure also provides pharmaceutical compositions comprising the compounds, uses and methods of treating certain disorders, such as cancer, including but not limited to Non-Small Cell Lung Cancer (NSCLC), colorectal cancer and/or pancreatic cancer.
  • NSCLC Non-Small Cell Lung Cancer
  • KRAS the Kirsten rat sarcoma viral oncogene homologue
  • KRAS protein has historically proven resistant to direct inhibition.
  • KRAS is a G-protein that couples extracellular mitogenic signaling to intracellular, pro-proliferative responses.
  • KRAS serves as an intracellular “on/off” switch. Mitogen stimulation induces the binding of GTP to KRAS, bringing about a conformational change which enables the interaction of KRAS with downstream effector proteins, leading to cellular proliferation.
  • GAPs GTPase- activating proteins
  • a pharmaceutical composition comprising a compound of Formula I or a pharmaceutically acceptable salt of said compound and a pharmaceutically acceptable excipient.
  • a compound of Formula I, or a pharmaceutically acceptable salt of said compound, or the pharmaceutical composition as described herein for use in treating cancer e.g., NSCLC, colorectal cancer or pancreatic cancer.
  • embodiment 2 is the compound according to embodiment 1, wherein L is C 1-6 alkylene (e.g., methylene or ethylene) substituted with 0-2 occurrences of R 2 .
  • embodiment 3 is the compound according to embodiment 1, wherein L is -O-C 1-6 alkylene (e.g., -O-methylene-, -O-ethylene- or -O-n-propylene) substituted with 0-2 occurrences of R 2 .
  • embodiment 4 is the compound according to embodiment 3, wherein L is -O-ethylene or -O-n-propylene substituted with 0-2 occurrences of R 2 .
  • embodiment 5 is the compound according to embodiment 4, wherein L is -O-ethylene substituted with 0 occurrences of R 2 .
  • embodiment 6 is the compound according to any one of embodiments 1-5, wherein R 1 is heterocycloalkyl substituted with 0-3 occurrences of R 5 .
  • embodiment 7 is the compound according to embodiment 6, wherein R 1 is 7-(hexahydro-1H-pyrrolizine) substituted with 0-3 occurrences of R 5 .
  • embodiment 8 is the compound according to embodiment 7, wherein R 1 is 7-(hexahydro-1H- pyrrolizine) substituted with 0 occurrences of R 5 .
  • embodiment 9 is the compound according to embodiment 7, wherein R 1 is 7-(hexahydro-1H-pyrrolizine) substituted with 1 occurrence of R 5 .
  • embodiment 10 is the compound according to embodiment 9, wherein R 5 is halogen (e.g., fluorine).
  • embodiment 11 is the compound according to embodiment 6, wherein R 1 is 2-pyrrolidine or 3-pyrrolidine substituted with 0-3 occurrences of R 5 .
  • embodiment 12 is the compound according to embodiment 11, wherein R 1 is 3- pyrrolidine substituted with 1 occurrence of R 5 .
  • embodiment 13 is the compound according to embodiment 12, wherein R 5 is cyano.
  • embodiment 14 is the compound according to embodiment 11, wherein R 1 is 3-pyrrolidine substituted with 2 occurrences of R 5 .
  • embodiment 15 is the compound according to embodiment 14, wherein one R 5 is methyl and the other R 5 is cyano.
  • embodiment 16 is the compound according to embodiment 11, wherein R 1 is 2-pyrrolidine substituted with 2 occurrences of R 5 .
  • embodiment 17 is the compound according to embodiment 16, wherein R 5 is C 1-4 alkyl (e.g., methyl), oxo, cyano or halogen (e.g., fluorine).
  • embodiment 18 is the compound according to embodiment 16, wherein one R 5 is methyl and the other R 5 is fluorine.
  • embodiment 19 is the compound according to embodiment 16, wherein one R 5 is methyl and the other R 5 is oxo.
  • embodiment 20 is the compound according to embodiment 3, wherein L is -O-n-propylene substituted with 2 occurrences of R 2 .
  • embodiment 21 is the compound according to embodiment 20, wherein the two R 2 are taken together with the same carbon atom to form a C 3-7 cycloalkyl (e.g., cyclopropyl).
  • embodiment 22 is the compound according to embodiment 21, wherein R 1 is heterocycloalkyl (e.g., N-morpholinyl) substituted with 0-3 occurrences of R 5 .
  • embodiment 23 is the compound according to embodiment 21, wherein R 1 is hydroxyl.
  • embodiment 24 is the compound according to any one of embodiments 1-23, wherein - , , , , Provided herein as embodiment 25 is the compound according to embodiment 24, r .
  • Provided herein as embodiment 26 is the compound according to embodiment 24, wherein -L-R 1 is .
  • Provided herein as embodiment 27 is the compound according to embodiment 24, wherein - .
  • embodiment 28 is the compound according to embodiment 24, wherein -L-R 1 is .
  • embodiment 29 is the compound according to embodiment 24, wherein -L .
  • embodiment 30 is the compound according to embodiment 24, wherein -L-R 1 is .
  • embodiment 31 is the compound according to embodiment 24, wherein -L-R 1 is .
  • embodiment 32 is the compound according to embodiment 24, wherein -L-R 1 is .
  • embodiment 33 is the compound according to embodiment 24, wherein -L-R 1 is .
  • embodiment 34 is the compound according to embodiment 24, wherein -L-R 1 is .
  • embodiment 35 is the compound according to embodiment 24, wherein -L-R 1 is .
  • embodiment 36 is the compound according to embodiment 24, wherein -L-R 1 is .
  • embodiment 37 is the compound according to embodiment 24, wherein -L-R 1 is .
  • embodiment 38 is the compound according to any one of embodiments 1-37, wherein R 3 is aryl (e.g., phenyl or naphthyl) substituted with 0-3 occurrences of R 6 .
  • embodiment 39 is the compound according to any one of embodiments 1-37, wherein R 3 is naphthyl substituted with 1 occurrence of R 6 .
  • embodiment 40 is the compound according to embodiment 39, wherein R 6 is halogen, amino, C 1-4 alkyl (e.g., methyl), C 1-4 haloalkyl (e.g., trifluoromethyl or difluoromethyl), hydroxyl or C 2-4 alkynyl (e.g., ethynyl).
  • R 6 is halogen, amino, C 1-4 alkyl (e.g., methyl), C 1-4 haloalkyl (e.g., trifluoromethyl or difluoromethyl), hydroxyl or C 2-4 alkynyl (e.g., ethynyl).
  • embodiment 41 is the compound according to embodiment 40, wherein R 6 is hydroxyl.
  • embodiment 42 is the compound according to embodiment 38, wherein R 3 is naphthyl substituted with 2 occurrences of R 6 .
  • embodiment 43 is the compound according to embodiment 42, wherein R 6 is C 1-4 alkyl, C 2-4 alkynyl, C 3-6 cycloalkyl, halogen, hydroxyl or -N(R z ) 2 .
  • embodiment 44 is the compound according to embodiment 43, wherein R 6 is ethyl, ethynyl, cyclopropyl, fluorine, chlorine, hydroxyl or -NH 2 .
  • embodiment 45 is the compound according to embodiment 43, wherein one R 6 is ethynyl and the other R 6 is hydroxyl.
  • embodiment 46 is the compound according to embodiment 43, wherein one R 6 is ethyl and the other R 6 is hydroxyl.
  • embodiment 47 is the compound according to embodiment 43, wherein one R 6 is ethyl and the other R 6 is fluorine.
  • embodiment 48 is the compound according to embodiment 43, wherein both R 6 are fluorine.
  • embodiment 49 is the compound according to embodiment 43, wherein one R 6 is cyclopropyl and the other R 6 is hydroxyl.
  • embodiment 50 is the compound according to embodiment 43, wherein one R 6 is fluorine and the other R 6 is hydroxyl.
  • embodiment 51 is the compound according to embodiment 43, wherein one R 6 is chlorine and the other R 6 is -NH 2 .
  • embodiment 52 is the compound according to embodiment 43, wherein one R 6 is ethynyl and the other R 6 is fluorine.
  • embodiment 53 is the compound according to embodiment 38, wherein R 3 is naphthyl substituted with 3 occurrences of R 6 .
  • embodiment 54 is the compound according to embodiment 53, wherein R 6 is C 1-4 alkyl, C 2-4 alkynyl, halogen or hydroxyl.
  • embodiment 55 is the compound according to embodiment 54, wherein R 6 is ethyl, ethynyl, fluorine or hydroxyl.
  • embodiment 56 is the compound according to embodiment 54, wherein one R 6 is hydroxyl, another R 6 is ethyl and the final R 6 is fluorine.
  • embodiment 57 is the compound according to embodiment 54, wherein one R 6 is hydroxyl, another R 6 is ethynyl and the final R 6 is fluorine.
  • embodiment 58 is the compound according to embodiment 54, wherein two R 6 are halogen (e.g., fluorine or chlorine) and the other R 6 is hydroxy.
  • embodiment 59 is the compound according to embodiment 38, wherein R 3 is phenyl substituted with 3 occurrences of R 6 .
  • embodiment 60 is the compound according to embodiment 59, wherein one R 6 is hydroxyl, another R 6 is cyclopropyl and the final R 6 is chlorine.
  • embodiment 61 is the compound according to any one of embodiments 1-37, wherein R 3 is heteroaryl (e.g., 4-(1H-indazole) or 4-benzo[d]thiazolyl) substituted with 0-3 occurrences of R 6 .
  • embodiment 62 is the compound according to embodiment 61, wherein R 3 is 4-(1H-indazole) substituted with 2 occurrences of R 6 .
  • embodiment 63 is the compound according to embodiment 62, wherein one R 6 is methyl and the other R 6 is chlorine.
  • embodiment 64 is the compound according to embodiment 61, wherein R 3 is 4-benzo[d]thiazolyl substituted with 2 occurrences of R 6 .
  • embodiment 65 is the compound according to embodiment 64, wherein one R 6 is fluorine and the other R 6 is -NH 2 .
  • embodiment 66 is the compound according to any one of embodiments 1-65, wherein R 3 is Provided herein as embodiment 67 is the compound according to embodiment 66, wherein R 3 is .
  • embodiment 68 is the compound according to embodiment 66, wherein R 3 is .
  • embodiment 69 is the compound according to embodiment 66, wherein R 3 is .
  • embodiment 70 is the compound according to embodiment 66, wherein .
  • embodiment 71 is the compound according to embodiment 66, wherein R 3 is .
  • embodiment 72 is the compound according to embodiment 66, wherein R 3 is .
  • embodiment 73 is the compound according to embodiment 66, wherein R 3 - 12 - is .
  • embodiment 74 is the compound according to embodiment 66, wherein R 3 is .
  • embodiment 75 is the compound according to embodiment 66, wherein R 3 is Provided herein as embodiment 76 is the compound according to embodiment 66, wherein R 3 i .
  • embodiment 77 is the compound according to embodiment 66, wherein R 3 is Provided herein as embodiment 78 is the compound according to embodiment 66, wherein R 3 is Provided herein as embodiment 79 is the compound according to embodiment 66, wherein R 3 is Provided herein as embodiment 80 is the compound according to embodiment 66, wherein Provided herein as embodiment 81 is the compound according to embodiment 66, wherein .
  • embodiment 82 is the compound according to embodiment 66, wherein .
  • embodiment 83 is the compound according to embodiment 66, wherein R 3 is .
  • embodiment 84 is the compound according to any one of embodiments 1-83, wherein W is N and --- is a single bond.
  • embodiment 85 is the compound according to any one of embodiments 1-84, wherein X is CH 2 .
  • embodiment 86 is the compound according to embodiment 85, wherein n is 0 and m is 0.
  • embodiment 87 is the compound according to embodiment 86, wherein p is 1.
  • embodiment 88 is the compound according to embodiment 87, wherein R x is 5-7 membered heteroaryl or -T-R y .
  • embodiment 89 is the compound according to embodiment 87, wherein R x is 5-7 membered heteroaryl substituted with 0-3 occurrences of R y .
  • embodiment 90 is the compound according to embodiment 89, wherein R x is 1-imidazolyl substituted with 0 occurrences of R y .
  • embodiment 91 is the compound according to embodiment 89, wherein -T-R y is -CH 2 OH, -C(O)NH 2 , -CH 2 C(O)NH 2 , -CH 2 S(O) 2 NH 2 or - S(O) 2 NH 2 .
  • embodiment 92 is the compound according to embodiment 86, wherein p is 2.
  • embodiment 93 is the compound according to embodiment 92, wherein each R x is hydroxyl, C 1-4 alkyl, -T-R y or two R x taken together with adjacent carbon atoms form 5-7 membered heterocycloalkyl substituted with 0-3 occurrences of R y .
  • embodiment 94 is the compound according to embodiment 93, wherein one R x is methyl and the other R x is hydroxyl.
  • embodiment 95 is the compound according to embodiment 93, wherein one R x is -C(O)NH 2 and the other R x is hydroxyl.
  • embodiment 96 is the compound according to embodiment 92, wherein two R x taken together with adjacent carbon atoms form a 1-tetrahydrofuranyl or 2- tetrahydrofuranyl substituted with 0 occurrences of R y .
  • embodiment 97 is the compound according to embodiment 86, wherein n is 1 and m is 0 or when n is 0 and m is 1.
  • embodiment 98 is the compound according to embodiment 97, wherein p is 0.
  • embodiment 99 is the compound according to embodiment 97, wherein p is 1.
  • embodiment 100 is the compound according to embodiment 99, wherein R x is hydroxyl or -T-R y .
  • embodiment 101 is the compound according to embodiment 100, wherein R x -T-R y is -CH 2 OH, -CH 2 S(O) 2 NH 2 , -C(O)NH 2 or -S(O) 2 NH 2 .
  • embodiment 102 is the compound according to embodiment 97, wherein p is 2.
  • embodiment 103 is the compound according to embodiment 102, wherein R x is hydroxyl, halogen, -T-R y or two R x are taken together with adjacent carbon atoms form a C 3-7 cycloalkyl or 5-7 membered heterocycloalkyl wherein each cycloalkyl or heterocycloalkyl is substituted with 0-3 occurrences of R y .
  • embodiment 104 is the compound according to embodiment 103, wherein both R x are hydroxyl.
  • embodiment 105 is the compound according to embodiment 103, wherein one R x is fluorine and the other is -CH 2 OH.
  • embodiment 106 is the compound according to embodiment 102, wherein two R x taken together with adjacent carbon atoms form a C 3-7 cycloalkyl or a 5-7 membered heterocycloalkyl substituted with 0-3 occurrences of R y .
  • embodiment 107 is the compound according to embodiment 106, wherein two R x taken together with adjacent carbon atoms form a cyclobutyl substituted with one occurrence of R y .
  • embodiment 108 is the compound according to embodiment 107, wherein R y is hydroxyl.
  • embodiment 109 is the compound according to embodiment 106, wherein two R x taken together with adjacent carbon atoms form a 1-tetrahydrofuranyl or 2-tetrahydrofuranyl substituted with 0 occurrences of R y .
  • embodiment 110 is the compound according to any one of e r .
  • embodiment 111 is the compound according to embodiment 110, w .
  • embodiment 112 is the compound according to embodiment 110, wherein .
  • embodiment 113 is the compound according to embodiment 110, wherein
  • embodiment 114 is the compound according to embodiment 110, wherein .
  • embodiment 115 is the compound according to embodiment 110, wherein .
  • embodiment 116 is the compound according to embodiment 110, wherein .
  • embodiment 117 is the compound according to embodiment 110, wherein is .
  • embodiment 118 is the compound according to embodiment 110, wherein .
  • embodiment 119 is the compound according to embodiment 110, wherein .
  • embodiment 120 is the compound according to embodiment 110, wherein Provided herein as embodiment 121 is the compound according to embodiment 110, wherein .
  • embodiment 122 is the compound according to embodiment 110, wherein is .
  • embodiment 123 is the compound according to embodiment 110, wherein .
  • embodiment 124 is the compound according to embodiment 110, wherein is .
  • embodiment 125 is the compound according to embodiment 110, wherein .
  • embodiment 126 is the compound according to embodiment 110, wherein is Provided herein as embodiment 127 is the compound according to embodiment 110, wherein s embodiment 128 is the compound according to embodiment 110, wherein is .
  • embodiment 129 is the compound according to embodiment 110, wherein .
  • embodiment 130 is the compound according to embodiment 110, wherein s .
  • embodiment 131 is the compound according to embodiment 110, wherein .
  • embodiment 132 is the compound according to embodiment 110, wherein .
  • embodiment 133 is the compound according to embodiment 110, wherein Provided herein as embodiment 134 is the compound according to embodiment 85, wherein n is 1 and m is 1.
  • embodiment 135 is the compound according to embodiment 134, wherein p is 0.
  • embodiment 136 is the compound according to embodiment 134, wherein p is 1.
  • embodiment 137 is the compound according to embodiment 136, wherein R x is hydroxyl, cyano, C 1-4 alkoxy, -N(R z ) 2 , 5-7 membered heteroaryl or -T-R y .
  • embodiment 138 is the compound according to embodiment 136, wherein R x is hydroxyl, cyano, methoxy, -NH 2 , 5-oxazolyl, 4-imidazolyl or 3-pyrazolyl.
  • embodiment 139 is the compound according to embodiment 137, wherein -T-R y is -NHC(O)OMe, -S(O) 2 Me, -NHC(O)Me, -NHC(O)-N(H)CH 2 CH 2 OMe, -CH 2 OH, -NHS(O) 2 Me, -CO 2 H, -C(O) 2 Me, 1-isopropanol, -S(O) 2 NH 2 , -C(O)NH 2 , -S(O) 2 N(H)Me or -C(O)N(H)Me.
  • embodiment 140 is the compound according to embodiment 134, wherein p is 2.
  • embodiment 141 is the compound according to embodiment 140, wherein R x is halogen, hydroxyl, C 1-4 alkyl, C 1-4 haloalkyl, C 1-4 alkoxy, C 3-7 cycloalkyl, -N(R z ) 2 or -T-R y or two R x taken together with the same carbon atom form a 5-7 membered heterocycloalkyl substituted with 0-3 occurrences of R y .
  • embodiment 142 is the compound according to embodiment 141, wherein one R x is fluorine and one R x is hydroxyl.
  • embodiment 143 is the compound according to embodiment 141, wherein one R x is methyl and one R x is hydroxyl.
  • embodiment 144 is the compound according to embodiment 141, wherein one R x is -NHS(O) 2 Me and one R x is methyl.
  • embodiment 145 is the compound according to embodiment 141, wherein one R x is -C(O)NH 2 and one R x is hydroxyl.
  • embodiment 146 is the compound according to embodiment 141, wherein one R x is methoxy and one R x is methyl.
  • embodiment 147 is the compound according to embodiment 141, wherein one R x is -NH 2 and one R x is methyl.
  • embodiment 148 is the compound according to embodiment 141, wherein one R x is -NHC(O)OMe and one R x is methyl.
  • embodiment 149 is the compound according to embodiment 141, wherein one R x is cyclopropyl and one R x is hydroxyl.
  • embodiment 150 is the compound according to embodiment 141, wherein one R x is trifluoromethyl and one R x is hydroxyl.
  • embodiment 151 is the compound according to embodiment 141, wherein one R x is difluoromethyl and one R x is hydroxyl.
  • embodiment 152 is the compound according to embodiment 141, wherein one R x is -C(O)NH 2 and one R x is methyl.
  • embodiment 153 is the compound according to embodiment 141, wherein one R x is -CH 2 OH and one R x is chloromethyl.
  • embodiment 154 is the compound according to embodiment 141, wherein both R x are hydroxyl.
  • embodiment 155 is the compound according to embodiment 140, wherein two R x are taken together with adjacent carbon atoms form a 5-7 membered heterocycloalkyl substituted with 0-3 occurrences of R y .
  • embodiment 156 is the compound according to embodiment 155, wherein two R x are taken together with adjacent carbon atoms to form 1-tetrahydrofuranyl substituted with 0 occurrences of R y .
  • embodiment 157 is the compound according to embodiment 155, wherein two R x are taken together with adjacent carbon atoms to form 1-pyrrolidinyl or 2-pyrrolidinyl substituted with 1 occurrence of R y .
  • embodiment 158 is the compound according to embodiment 157, wherein R y is oxo.
  • embodiment 159 is the compound according to embodiment 134, wherein p is 3.
  • embodiment 160 is the compound according to embodiment 159, wherein one R x is hydroxyl, halogen, oxo, C 1-4 alkyl or two R x taken together with adjacent carbon atoms can form C 3-7 cycloalkyl substituted with 0-3 occurrences of R y or two R x taken together can form a bridged ring further substituted with 0- 2 occurrences of R y .
  • embodiment 161 is the compound according to embodiment 160, wherein one R x is hydroxyl and the other two R x are methyl.
  • embodiment 162 is the compound according to embodiment 160, wherein one R x is hydroxyl and the other two R x are fluorine.
  • embodiment 163 is the compound according to embodiment 160, wherein one R x is -C(O)NH 2 and the other two R x are methyl.
  • embodiment 164 is the compound according to embodiment 160, wherein one R x is oxo and the other two R x are fluorine.
  • embodiment 165 is the compound according to embodiment 160, wherein one R x is hydroxyl and the other two R x taken together with adjacent carbon atoms form cyclopropyl substituted with 0 occurrences of R y .
  • embodiment 166 is the compound according to embodiment 160, wherein one R x is hydroxyl and the other two R x taken together form an ethylene or methylene bridge substituted with 0 occurrences of R y .
  • embodiment 167 is the compound according to embodiment 160, wherein one R x is C(O)NH 2 and the other two R x taken together form an ethylene substituted with 0 occurrences of R y .
  • embodiment 168 is the compound according to any one of ,
  • embodiment 169 is the compound according to embodiment 168, wherein .
  • embodiment 170 is the compound according to embodiment 168, wherein .
  • d herein as embodiment 171 is the compound according to embodiment 168, wherein .
  • embodiment 172 is the compound according to embodiment 168, wherein .
  • embodiment 173 is the compound according to embodiment 168, wherein is mbodiment 174 is the compound according to embodiment 168, wherein .
  • embodiment 175 is the compound according to embodiment 168, wherein .
  • embodiment 176 is the compound according to embodiment 168, wherein .
  • embodiment 177 is the compound according to embodiment 168, wherein .
  • embodiment 178 is the compound according to embodiment 168, wherein .
  • embodiment 179 is the compound according to embodiment 168, wherein is .
  • embodiment 180 is the compound according to embodiment 168, wherein Provided herein as embodiment 181 is the compound according to embodiment 168, wherein .
  • embodiment 182 is the compound according to embodiment 168, wherein .
  • embodiment 183 is the compound according to embodiment 168, wherein .
  • embodiment 184 is the compound according to embodiment 168, wherein .
  • embodiment 185 is the compound according to embodiment 168, wherein .
  • embodiment 186 is the compound according to embodiment 168, wherein .
  • embodiment 187 is the compound according to embodiment 168, wherein .
  • embodiment 188 is the compound according to embodiment 168, wherein Provided herein as embodiment 189 is the compound according to embodiment 168, wherein .
  • embodiment 190 is the compound according to embodiment 168, wherein .
  • embodiment 191 is the compound according to embodiment 168, wherein .
  • embodiment 192 is the compound according to embodiment 168, wherein .
  • embodiment 193 is the compound according to embodiment 168, wherein .
  • embodiment 194 is the compound according to embodiment 168, wherein .
  • embodiment 195 is the compound according to embodiment 168, wherein .
  • embodiment 196 is the compound according to embodiment 168, wherein is Provided herein as embodiment 197 is the compound according to embodiment 168, wherein .
  • embodiment 198 is the compound according to embodiment 168, wherein is .
  • embodiment 199 is the compound according to embodiment 168, wherein .
  • embodiment 200 is the compound according to embodiment 168, wherein is .
  • embodiment 201 is the compound according to embodiment 168, wherein Provided herein as embodiment 202 is the compound according to embodiment 168, wherein .
  • Provided herein as embodiment 203 is the compound according to embodiment 168, wherein Provided herein as embodiment 204 is the compound according to embodiment 168, wherein .
  • embodiment 205 is the compound according to embodiment 168, wherein .
  • embodiment 206 is the compound according to embodiment 168, wherein .
  • embodiment 207 is the compound according to embodiment 168, wherein .
  • embodiment 208 is the compound according to embodiment 168, wherein .
  • Provided herein as embodiment 209 is the compound according to embodiment 168, wherein Provided herein as embodiment 210 is the compound according to embodiment 168, wherein .
  • embodiment 211 is the compound according to embodiment 168, wherein is .
  • embodiment 212 is the compound according to embodiment 168, wherein .
  • Provided herein as embodiment 213 is the compound according to embodiment 168, wherein is .
  • embodiment 214 is the compound according to embodiment 168, wherein .
  • embodiment 215 is the compound according to embodiment 168, wherein is Provided herein as embodiment 216 is the compound according to embodiment 168, wherein .
  • embodiment 217 is the compound according to embodiment 168, wherein is .
  • embodiment 218 is the compound according to embodiment 168, wherein .
  • embodiment 219 is the compound according to embodiment 168, wherein is .
  • embodiment 220 is the compound according to embodiment 168, wherein .
  • embodiment 221 is the compound according to embodiment 168, wherein s Provided herein as embodiment 222 is the compound according to embodiment 1 Provided herein as embodiment 223 is the compound according to embodiment 168, wherein .
  • Provided herein as embodiment 224 is the compound according to embodiment 168, wherein .
  • Provided herein as embodiment 225 is the compound according to embodiment 168, wherein .
  • Provided herein as embodiment 226 is the compound according to embodiment 168, wherein .
  • Provided herein as embodiment 227 is the compound according to embodiment 168, wherein .
  • Provided herein as embodiment 228 is the compound according to embodiment 168, wherein Provided herein as embodiment 229 is the compound according to embodiment 168, wherein .
  • embodiment 230 is the compound according to embodiment 168, wherein .
  • embodiment 231 is the compound according to embodiment 168, wherein .
  • embodiment 232 is the compound according to embodiment 168, wherein is .
  • embodiment 233 is the compound according to embodiment 168, wherein .
  • embodiment 234 is the compound according to embodiment 168, wherein is Provided herein as embodiment 235 is the compound according to embodiment 168, wherein .
  • embodiment 236 is the compound according to embodiment 168, wherein is Provided herein as embodiment 237 is the compound according to embodiment 168, wherein .
  • embodiment 238 is the compound according to embodiment 168, wherein s .
  • embodiment 239 is the compound according to embodiment 168, wherein .
  • embodiment 240 is the compound according to embodiment 85, wherein n is 1 and m is 2 or n is 2 and m is 1.
  • embodiment 241 is the compound according to embodiment 240, wherein p is 0.
  • embodiment 242 is the compound according to embodiment 420, wherein p is 1.
  • embodiment 243 is the compound according to embodiment 242, wherein R x is C 1-4 alkyl, C 1-4 alkenyl, cyano, hydroxyl, oxo, -N(R z ) 2 or -T-R y .
  • embodiment 244 is the compound according to embodiment 243, wherein R x is cyano, methyl, oxo, hydroxyl, -NH 2 , methenyl, -SO 2 NH 2 , -NHC(O)Me or -NHC(O)CF 2 H.
  • embodiment 245 is the compound according to embodiment 240, wherein p is 2.
  • embodiment 246 is the compound according to embodiment 245, wherein R x is hydroxy, C 1-4 alkyl, halogen or two R x are taken together to form a C 1-4 alkylene bridged ring further substituted with 0-2 occurrences of R y .
  • embodiment 247 is the compound according to embodiment 246, wherein both R x are fluorine.
  • embodiment 248 is the compound according to embodiment 246, wherein one R x is hydroxyl and the other R x is methyl.
  • embodiment 249 is the compound according to embodiment 246, wherein two R x are taken together to form a bridged ring wherein the bridge is methylene further substituted with 0 occurrences of R y .
  • embodiment 250 is the compound according to embodiment 246, wherein two R x are taken together to form a bridged ring wherein the bridge is methylene further substituted with one occurrence of R y .
  • embodiment 251 is the compound according to embodiment 250, wherein R y is hydroxyl.
  • embodiment 252 is the compound according to embodiment 246, wherein two R x are taken together to form a bridged ring wherein the bridge is methylene further substituted with 2 occurrences of R y .
  • embodiment 253 is the compound according to embodiment 252, wherein each R y is methyl or hydroxyl.
  • embodiment 254 is the compound according to embodiment 240, wherein p is 3.
  • embodiment 255 is the compound according to embodiment 254, wherein R x is hydroxy, oxo, halogen or two R x are taken together to form a C 1-4 alkylene bridged ring further substituted with 0-2 occurrences of R y .
  • embodiment 256 is the compound according to embodiment 255, wherein one R x is oxo and the other two R x are fluorine.
  • embodiment 257 is the compound according to embodiment 255, wherein one R x is hydroxyl and the other two R x are fluorine.
  • embodiment 258 is the compound according to embodiment 255, wherein one R x is hydroxy and the other two R x are taken together to form a bridged ring wherein the bridge is methylene further substituted with 0 occurrences of R y .
  • embodiment 259 is the compound according to embodiment 85, wherein n is 2 and m is 2.
  • embodiment 260 is the compound according to embodiment 259, wherein p is 0.
  • embodiment 261 is the compound according to embodiment 259, wherein p is 2.
  • embodiment 262 is the compound according to embodiment 261, wherein two R x are taken together to form a bridged ring wherein the bridge is -O-.
  • embodiment 263 is the compound according to any one of , .
  • embodiment 264 is the compound according to embodiment 263, wherein Provided herein as embodiment 265 is the compound according to embodiment 263, wherein .
  • embodiment 266 is the compound according to embodiment 263, wherein is .
  • embodiment 267 is the compound according to embodiment 263, wherein .
  • embodiment 268 is the compound according to embodiment 263, wherein .
  • embodiment 269 is the compound according to embodiment 263, wherein .
  • embodiment 270 is the compound according to embodiment 263, wherein .
  • embodiment 271 is the compound according to embodiment 263, wherein Provided herein as embodiment 272 is the compound according to embodiment 263, wherein .
  • embodiment 273 is the compound according to embodiment 263, wherein .
  • embodiment 274 is the compound according to embodiment 263, wherein .
  • embodiment 275 is the compound according to embodiment 263, wherein .
  • embodiment 276 is the compound according to embodiment 263, wherein .
  • embodiment 277 is the compound according to embodiment 263, wherein .
  • embodiment 278 is the compound according to embodiment 263, wherein .
  • embodiment 279 is the compound according to embodiment 263, wherein is Provided herein as embodiment 280 is the compound according to embodiment 263, wherein .
  • embodiment 281 is the compound according to embodiment 263, wherein .
  • embodiment 282 is the compound according to embodiment 263, wherein .
  • embodiment 283 is the compound according to embodiment 263, wherein .
  • embodiment 284 is the compound according to embodiment 263, wherein is Provided herein as embodiment 285 is the compound according to embodiment 263, wherein Provided herein as embodiment 286 is the compound according to embodiment 263, wherein d herein as embodiment 287 is the compound according to embodiment 263, wherein .
  • embodiment 288 is the compound according to embodiment 263, wherein .
  • embodiment 289 is the compound according to embodiment 263, wherein is .
  • embodiment 290 is the compound according to embodiment 263, wherein .
  • embodiment 291 is the compound according to embodiment 263, wherein .
  • embodiment 292 is the compound according to embodiment 263, wherein
  • embodiment 293 is the compound according to embodiment 263, wherein .
  • embodiment 294 is the compound according to embodiment 263, wherein is .
  • embodiment 296 is the compound according to embodiment 295, wherein n is 0 and m is 1.
  • embodiment 297 is the compound according to embodiment 296, wherein p is 1.
  • embodiment 298 is the compound according to embodiment 297, wherein R x is hydroxyl.
  • embodiment 299 is the compound according to embodiment 295, wherein n is 1 and m is 1.
  • embodiment 300 is the compound according to embodiment 299, wherein p is 0.
  • embodiment 301 is the compound according to embodiment 299, wherein p is 1.
  • embodiment 302 is the compound according to embodiment 301, wherein R x is oxo or hydroxyl.
  • embodiment 303 is the compound according to any one of e .
  • embodiment 304 is the compound according to any one of embodiments 1-303, wherein R 4 is C 1-4 alkyl, C 1-4 alkoxy, hydroxyl, halogen or C 1-4 haloalkyl.
  • embodiment 305 is the compound according to embodiment 304, wherein R 4 is C 1-4 alkyl or halogen.
  • embodiment 306 is the compound according to embodiment 305, wherein R 4 is fluorine.
  • embodiment 307 is the compound according to embodiment 1, wherein is the compound is a compound of formula (II):
  • embodiment 308 is the compound according to embodiment 1, wherein is the compound is a compound of formula (III):
  • embodiment 309 is the compound according to embodiment 1, wherein is the compound is a compound of formula (IV):
  • embodiment 310 is the compound according to embodiment 1, wherein is the compound is a compound of formula (V):
  • embodiment 311 is the compound according to embodiment 1, wherein the compound is not: 1-(7-(8-chloronaphthalen-1-yl)-8-fluoro-2-((hexahydro-1H-pyrrolizin-7a- yl)methoxy)pyrido[4,3- d]pyrimidin-4-yl)-3-methylpiperidin-3-ol; (S)-1-(7-(8-ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorohexahydro- 1H-pyrrolizin-7a-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3- methylpiperidin-3-ol; (R)-1-(7-(8-eth)-8-fluoro-2-((
  • embodiment 312 is the compound according to embodiment 1, wherein the compound is not: 1-(7-(8-chloronaphthalen-1-yl)-8-fluoro-2-((hexahydro-1H-pyrrolizin-7a- yl)methoxy)pyrido[4,3- d]pyrimidin-4-yl)-3-methylpiperidin-3-ol; (S)-1-(7-(8-ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorohexahydro- 1H-pyrrolizin-7a-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3- methylpiperidin-3-ol; (R)-1-(7-(8-ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7
  • embodiment 313 is the compound according to embodiment 1, wherein the compound is selected from one of the following compounds: 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro- 1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)azepan-3-one; (R)-1-(7-(8-Ethyl-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H- pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3-methylpiperidin-3-ol; (R)-1-(7-(8-Cyclopropyl-3-hydroxynaphthalen
  • embodiment 314 is the compound according to embodiment 1, wherein the compound is selected from one of the following compounds: 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro- 1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)azepan-3-one; (R)-1-(7-(8-Cyclopropyl-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3- methylpiperidin-3-ol; 3-(Difluoromethyl)-1-(7-(8-ethyl-7
  • embodiment 315 is the compound according to embodiment 1, wherein the compound is selected from one of the following compounds: (R)-1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)piperidine-3- sulfonamide; 4-(4-(Azepan-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)- yl)methoxy)pyrido[4,3-d]pyrimidin-7-yl)-5-ethyl-6-fluoronaphthalen-2-ol; 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-y
  • embodiment 316 is the compound according to embodiment 1, wherein the compound is selected from one of the following compounds: 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro- 1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)azepan-3-one; (R)-1-(7-(8-Cyclopropyl-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3- methylpiperidin-3-ol; 3-(Difluoromethyl)-1-(7-(8-ethyl-7
  • embodiment 317 is the compound according to embodiment 1, wherein the compound is selected from one of the following compounds: 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro- 1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)azepan-3-one; (R)-1-(7-(8-Cyclopropyl-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3- methylpiperidin-3-ol; 3-(Difluoromethyl)-1-(7-(8-ethyl-7
  • embodiment 318 is the compound according to embodiment 1, wherein the compound is selected from one of the following compounds: 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro- 1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)azepan-3-one; (R)-1-(7-(8-Cyclopropyl-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3- methylpiperidin-3-ol; 3-(Difluoromethyl)-1-(7-(8-ethyl-7
  • embodiment 319 is the compound according to embodiment 1, wherein the compound is selected from one of the following compounds: 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro- 1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3-(fluoromethyl)piperidin-3- ol (Isomer 1); (R)-1-(7-(8-Ethyl-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H- pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3-methylpiperidin-3-ol; (3R)-1-(7-(7-(8
  • embodiment 320 is the compound according to embodiment 1, wherein the compound is selected from one of the following compounds: (R)-1-(7-(8-Ethyl-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H- pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3-methylpiperidin-3-ol; (R)-1-(7-(8-Cyclopropyl-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-3- methylpiperidin-3-ol; 3-(Difluoromethyl)-1-(7-(8-ethyl-3-
  • embodiment 321 is the compound according to embodiment 1, wherein the compound is not example 1, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 21, 22, 23, 25, 27, 28, 30, 31, 32, 33, 39, 40, 41, 44, 51, 53, 54, 55, 56, 58, 59, 65, 66, 67, 68, 69, 71, 75, 76, 81, 82, 86, 87, 89, 101, 104, 106, 108, 109, 112, 113, 116, 117, 120, 123, 129, 130, 131, 132, 134, 137, 138, 140, 144, 145, 147, 151, 153, 154, 170, 172, 173, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 197, 202, 203, 213, 221, 228, 237, 239, 240
  • WO 2022/132200 International Application No. PCT/US2021/010065.
  • embodiment 322 is the compound according to embodiment 1, wherein the compound is not example 1, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 21, 22, 23, 25, 27, 28, 30, 31, 32, 33, 39, 40, 41, 44, 51, 53, 54, 55, 56, 58, 59, 65, 66, 67, 68, 69, 71, 75, 76, 81, 82, 86, 87, 89, 101, 104, 106, 108, 109, 112, 113, 116, 117, 120, 123, 129, 130, 131, 132, 134, 137, 138, 140, 144, 145, 147, 151, 153, 154, 170, 172, 173, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193,
  • WO 2022/132200 International Application No. PCT/US2021/010065.
  • a pharmaceutical composition comprising a compound disclosed herein in combination with one or more pharmaceutically acceptable excipients, such as diluents, carriers, adjuvants and the like, and, if desired, other active ingredients.
  • a pharmaceutical composition comprises a therapeutically effective amount of a compound disclosed herein.
  • the compound(s) disclosed herein may be administered by any suitable route in the form of a pharmaceutical composition adapted to such a route and in a dose effective for the treatment intended.
  • the compounds and compositions presented herein may, for example, be administered orally, mucosally, topically, transdermally, rectally, pulmonarily, parentally, intranasally, intravascularly, intravenously, intraarterial, intraperitoneally, intrathecally, subcutaneously, sublingually, intramuscularly, intrasternally, vaginally or by infusion techniques, in dosage unit formulations containing conventional pharmaceutically acceptable excipients.
  • the pharmaceutical composition may be in the form of, for example, a tablet, chewable tablet, minitablet, caplet, pill, bead, hard capsule, soft capsule, gelatin capsule, granule, powder, lozenge, patch, cream, gel, sachet, microneedle array, syrup, flavored syrup, juice, drop, injectable solution, emulsion, microemulsion, ointment, aerosol, aqueous suspension, or oily suspension.
  • the pharmaceutical composition is typically made in the form of a dosage unit containing a particular amount of the active ingredient.
  • embodiment 323 is a pharmaceutical composition comprising the compound according to any one of embodiments 1-322, or a tautomer thereof, or a pharmaceutically acceptable salt of said compound or said tautomer, and a pharmaceutically acceptable excipient.
  • embodiment 324 is a compound according to any one of Embodiments 1-322, or a tautomer thereof, or a pharmaceutically acceptable salt of said compound or said tautomer, or the pharmaceutical composition according to embodiment 323 for use as a medicament.
  • the compounds described herein are to be understood to include all stereoisomers, tautomers, or pharmaceutically acceptable salts of any of the foregoing or solvates of any of the foregoing. Accordingly, the scope of the methods and uses provided in the instant disclosure is to be understood to encompass also methods and uses employing all such forms.
  • the compounds provided herein may be useful for veterinary treatment of companion animals, exotic animals and farm animals, including mammals, rodents, and the like. For example, animals including horses, dogs, and cats may be treated with compounds provided herein.
  • the disclosure provides methods of using the compounds or pharmaceutical compositions of the present disclosure to treat disease conditions, including but not limited to conditions implicated by KRAS G12D, G12V, G12A, G12S or G12C mutation (e.g., cancer).
  • the cancer types are non-small cell lung cancer, colorectal cancer, pancreatic cancer, appendiceal cancer, endometrial cancer, esophageal cancer, cancer of unknown primary, ampullary cancer, gastric cancer, small bowel cancer, sinonasal cancer, bile duct cancer, or melanoma.
  • KRAS G12D mutations occur with the alteration frequencies shown in the table below (TCGA data sets; 1-3 For example, the table shows that 32.4% of subjects with pancreatic cancer have a cancer wherein one or more cells express KRAS G12D mutant protein. Accordingly, the compounds provided herein, which bind to KRAS G12D (see Section entitled “Biological Evaluation” below) are useful for treatment of subjects having a cancer, including, but not limited to the cancers listed in the table below.
  • embodiment 325 is a compound according to any one of embodiments 1-322 or a pharmaceutically acceptable salt thereof, or the pharmaceutical composition according to embodiment 323 for use in treating cancer.
  • Embodiment 326 is a compound according to any one of Embodiments 1-322 or a pharmaceutically acceptable salt thereof, or the pharmaceutical composition according to Embodiment 323 for use in treating cancer, wherein one or more cells express KRAS G12D, G12V, G12A, G12S or G12C mutant protein.
  • Embodiment 327 is the compound or pharmaceutical composition for use of Embodiment 325 or 326, wherein the cancer is pancreatic cancer, colorectal cancer, non-small cell lung cancer, small bowel cancer, appendiceal cancer, cancer of unknown primary, endometrial cancer, mixed cancer types, hepatobiliary cancer, small cell lung cancer, cervical cancer, germ cell cancer, ovarian cancer, gastrointestinal neuroendocrine cancer, bladder cancer, myelodysplastic/myeloproliferative neoplasms, head and neck cancer, esophagogastric cancer, soft tissue sarcoma, mesothelioma, thyroid cancer, leukemia, or melanoma.
  • the cancer is pancreatic cancer, colorectal cancer, non-small cell lung cancer, small bowel cancer, appendiceal cancer, cancer of unknown primary, endometrial cancer, mixed cancer types, hepatobiliary cancer, small cell lung cancer, cervical cancer, germ cell cancer, ovarian cancer,
  • Embodiment 328 is a use of the compound according to any one of Embodiments 1-322 or a pharmaceutically acceptable salt thereof, or the pharmaceutical composition according to Embodiment 323 in the preparation of a medicament for treating cancer.
  • Embodiment 329 is a use of the compound according to any one of Embodiments 1-322 or a pharmaceutically acceptable salt thereof, or the pharmaceutical composition according to Embodiment 323 in the preparation of a medicament for treating cancer, wherein one or more cells express KRAS G12D, G12V, G12A, G12S or G12C mutant protein.
  • Embodiment 330 is the use according to Embodiment 328 or 329, wherein the cancer is non-small cell lung cancer, small bowel cancer, appendiceal cancer, colorectal cancer, cancer of unknown primary, endometrial cancer, mixed cancer types, pancreatic cancer, hepatobiliary cancer, small cell lung cancer, cervical cancer, germ cell cancer, ovarian cancer, gastrointestinal neuroendocrine cancer, bladder cancer, myelodysplastic/myeloproliferative neoplasms, head and neck cancer, esophagogastric cancer, soft tissue sarcoma, mesothelioma, thyroid cancer, leukemia, or melanoma.
  • the cancer is non-small cell lung cancer, small bowel cancer, appendiceal cancer, colorectal cancer, cancer of unknown primary, endometrial cancer, mixed cancer types, pancreatic cancer, hepatobiliary cancer, small cell lung cancer, cervical cancer, germ cell cancer, ovarian cancer, gastrointestinal neuroendoc
  • Embodiment 331 is a method of treating cancer in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the compound according to any one of to any one of Embodiments 1-322 or a pharmaceutically acceptable salt thereof.
  • Embodiment 332 is a method of treating cancer in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of the compound according to any one of to any one of Embodiments 1-322 or a pharmaceutically acceptable salt thereof, wherein one or more cells express KRAS G12D, G12V, G12A, G12S or G12C mutant protein.
  • Embodiment 333 is the method according to Embodiment 331 or 332, wherein the cancer is non-small cell lung cancer, small bowel cancer, appendiceal cancer, colorectal cancer, cancer of unknown primary, endometrial cancer, mixed cancer types, pancreatic cancer, hepatobiliary cancer, small cell lung cancer, cervical cancer, germ cell cancer, ovarian cancer, gastrointestinal neuroendocrine cancer, bladder cancer, myelodysplastic/myeloproliferative neoplasms, head and neck cancer, esophagogastric cancer, soft tissue sarcoma, mesothelioma, thyroid cancer, leukemia, or melanoma.
  • the cancer is non-small cell lung cancer, small bowel cancer, appendiceal cancer, colorectal cancer, cancer of unknown primary, endometrial cancer, mixed cancer types, pancreatic cancer, hepatobiliary cancer, small cell lung cancer, cervical cancer, germ cell cancer, ovarian cancer, gastrointestinal neuroendocrine
  • Embodiment 334 is the method according to Embodiment 332 or 333, wherein the cancer is non-small cell lung cancer, colorectal cancer, pancreatic cancer, appendiceal cancer, endometrial cancer, esophageal cancer, cancer of unknown primary, ampullary cancer, gastric cancer, small bowel cancer, sinonasal cancer, bile duct cancer, or melanoma.
  • Embodiment 335 is the method according to Embodiment 334, wherein the cancer is non-small cell lung cancer.
  • Embodiment 336 is the method according to Embodiment 334, wherein the cancer is colorectal cancer.
  • Embodiment 337 is the method according to Embodiment 334, wherein the cancer is pancreatic cancer.
  • Embodiment 338 is the method according to anyone of Embodiments 331-337, wherein the subject has a cancer that was determined to have one or more cells expressing the KRAS G12D, G12V, G12A, G12S or G12C mutant protein prior to administration of the compound or a pharmaceutically acceptable salt thereof.
  • Combination Therapy The present disclosure also provides methods for combination therapies in which an agent known to modulate other pathways, or other components of the same pathway, or even overlapping sets of target enzymes are used in combination with a compound of the present disclosure or a pharmaceutically acceptable salt thereof.
  • such therapy includes but is not limited to the combination of one or more compounds of the disclosure with chemotherapeutic agents, therapeutic antibodies, and radiation treatment, to provide a synergistic or additive therapeutic effect.
  • chemotherapeutic agents include but is not limited to the combination of one or more compounds of the disclosure with chemotherapeutic agents, therapeutic antibodies, and radiation treatment, to provide a synergistic or additive therapeutic effect.
  • chemotherapeutic agents include but is not limited to the combination of one or more compounds of the disclosure with chemotherapeutic agents, therapeutic antibodies, and radiation treatment, to provide a synergistic or additive therapeutic effect.
  • Embodiment 339 is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an Aurora kinase A inhibitor, AKT inhibitor, arginase inhibitor, CDK4/6 inhibitor, ErbB family inhibitor, ERK inhibitor, FAK inhibitor, FGFR inhibitor, glutaminase inhibitor, IGF- 1R inhibitor, KIF18A inhibitor, MCL-1 inhibitor, MEK inhibitor, mTOR inhibitor, PD-1 inhibitor, PD-L1 inhibitor, PI3K inhibitor, Raf kinase inhibitor, SHP2 inhibitor, SOS1 inhibitor, Src kinase inhibitor, or one or more chemotherapeutic agent.
  • the second compound is an Aurora kinase A inhibitor, AKT inhibitor, arginase inhibitor, CDK4/6 inhibitor, ErbB family inhibitor, ERK inhibitor, FAK inhibitor, FGFR inhibitor, glutaminase inhibitor, IGF- 1R inhibitor, K
  • the second compound is administered as a pharmaceutically acceptable salt. In another embodiment the second compound is administered as a pharmaceutical composition comprising the second compound or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable excipient.
  • Aurora Kinase A Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an Aurora kinase A inhibitor.
  • Aurora kinase A inhibitors for use in the methods provided herein include, but are not limited to, alisertib, cenisertib, danusertib, tozasertib, LY3295668 ((2R,4R)-1-[(3-chloro-2-fluorophenyl)methyl]-4-[[3-fluoro-6-[(5-methyl-1H-pyrazol-3- yl)amino]pyridin-2-yl]methyl]-2-methylpiperidine-4-carboxylic acid), ENMD-2076 (6-(4- methylpiperazin-1-yl)-N-(5-methyl-1H-pyrazol-3-yl)-2-[(E)-2-phenylethenyl]pyrimidin-4- amine), TAK-901 (5-(3-ethylsulfonylphenyl)-3,8-dimethyl-N-(1-methylpiperidin-4-yl)-9H- pyr
  • AKT Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an AKT inhibitor.
  • Exemplary AKT inhibitors for use in the methods provided herein include, but are not limited to, afuresertib, capivasertib, ipatasertib, uprosertib, BAY1125976 (2-[4-(1- aminocyclobutyl)phenyl]-3-phenylimidazo[1,2-b]pyridazine-6-carboxamide), ARQ 092 (3- [3-[4-(1-aminocyclobutyl)phenyl]-5-phenylimidazo[4,5-b]pyridin-2-yl]pyridin-2-amine), MK2206 (8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-2H-[1,
  • Arginase Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an arginase inhibitor.
  • Exemplary arginase inhibitors for use in the methods provided herein include, but are not limited to, numidargistat and CB 280.
  • CDK4/6 Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a CDK4/6 inhibitor.
  • CDK 4/6 refers to cyclin dependent kinases (“CDK”) 4 and 6, which are members of the mammalian serine/threonine protein kinases.
  • CDK 4/6 inhibitor refers to a compound that is capable of negatively modulating or inhibiting all or a portion of the enzymatic activity of CDK 4 and/or 6.
  • CDK 4/6 inhibitors for use in the methods provided herein include, but are not limited to, abemaciclib, palbociclib, ribociclib, trilaciclib, and PF-06873600 ((pyrido[2,3-d]pyrimidin-7(8H)-one, 6-(difluoromethyl)-8-[(1R,2R)-2-hydroxy-2- methylcyclopentyl]-2-[[1-(methylsulfony1)-4-piperidinyl]amino]).
  • the CDK4/6 inhibitor is palbociclib.
  • ErbB Family Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an ErbB family inhibitor.
  • the term “ErbB family” as used herein refers to a member of a mammalian transmembrane protein tyrosine kinase family including: ErbB1 (EGFR HER1), ErbB2 (HER2), ErbB3 (HER3), and ErbB4 (HER4).
  • ErbB family inhibitor refers to an agent, e.g., a compound or antibody, that is capable of negatively modulating or inhibiting all or a portion of the activity of at least one member of the ErbB family.
  • the modulation or inhibition of one or more ErbB tyrosine kinase may occur through modulating or inhibiting kinase enzymatic activity of one or more ErbB family member or by blocking homodimerization or heterodimerization of ErbB family members.
  • the ErbB family inhibitor is an EGFR inhibitor, e.g., an anti- EGFR antibody.
  • Exemplary anti-EGFR antibodies for use in the methods provided herein include, but are not limited to, zalutumumab, nimotuzumab, matuzumab, necitumumab, panitumumab, and cetuximab.
  • the anti-EGFR antibody is cetuximab.
  • the anti-EGFR antibody is panitumumab.
  • the ErbB family inhibitor is a HER2 inhibitor, e.g., an anti- HER2 antibody.
  • Exemplary anti-HER-2 antibodies for use in the methods provided herein include, but are not limited to, pertuzumab, trastuzumab, and trastuzumab emtansine.
  • the ErbB family inhibitor is a HER3 inhibitor, e.g., an anti-HER3 antibody, such as HMBD-001 (Hummingbird Bioscience).
  • the ErbB family inhibitor is a combination of an anti-EGFR antibody and anti-HER2 antibody.
  • the ErbB family inhibitor is an irreversible inhibitor.
  • Exemplary irreversible ErbB family inhibitors for use in the methods provided herein include, but are not limited to, afatinib, dacomitinib, canertinib, poziotinib, AV 412 ((N-[4-[(3-chloro-4- fluorophenyl)amino]-7-[3-methyl-3-(4-methyl-1-piperazinyl)-1-butyn-1-yl]-6-quinazolinyl]- 2-propenamide)), PF 6274484 ((N-[4-[(3-chloro-4-fluorophenyl)amino]-7-methoxy-6- quinazolinyl]-2-propenamide), and HKI 357 ((E)-N-[4-[3-chloro-4-[(3- fluorophenyl)methoxy]anilino]-3-cyano-7-ethoxyquinolin-6-yl]-4-(di
  • the irreversible ErbB family inhibitor is afatinib. In one embodiment, the irreversible ErbB family inhibitor is dacomitinib. In one embodiment, the ErbB family inhibitor is a reversible inhibitor.
  • Exemplary reversible ErbB family inhibitors for use in the methods provided herein include, but are not limited to erlotinib, gefitinib, sapitinib, varlitinib, tarloxotinib, TAK-285 (N-(2-(4-((3-chloro- 4-(3-(trifluoromethyl)phenoxy)phenyl)amino)-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethyl)-3- hydroxy-3-methylbutanamide), AEE788 ((S)-6-(4-((4-ethylpiperazin-1-yl)methyl)phenyl)-N- (1-phenylethyl)-7H-pyrrolo[2,
  • the reversible ErbB family inhibitor is sapitinib. In one embodiment, the reversible ErbB family inhibitor is tarloxotinib.
  • ERK Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an ERK inhibitor.
  • Exemplary ERK inhibitors for use in the methods provided herein include, but are not limited to, ulixertinib, ravoxertinib, CC-90003 (N-[2-[[2-[(2-methoxy-5-methylpyridin-4- yl)amino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]-5-methylphenyl]prop-2-enamide), LY3214996 (6,6-dimethyl-2-[2-[(2-methylpyrazol-3-yl)amino]pyrimidin-4-yl]-5-(2- morpholin-4-ylethyl)thieno[2,3-c]pyrrol-4-one), KO-947 (1,5,6,8-tetrahydro-6- (phenylmethyl)-3-(4-pyridinyl)-7H-pyrazolo[4,3-g]quinazolin-7-one), ASTX029, LTT462, and JSI-1187.
  • FAK Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a FAK inhibitor.
  • Exemplary FAK inhibitors for use in the methods provided herein include, but are not limited to, GSK2256098 (2-[[5-chloro-2-[(5-methyl-2-propan-2-ylpyrazol-3- yl)amino]pyridin-4-yl]amino]-N-methoxybenzamide), PF-00562271 (N-methyl-N-[3-[[[2- [(2-oxo-1,3-dihydroindol-5-yl)amino]-5-(trifluoromethyl)pyrimidin-4- yl]amino]methyl]pyridin-2-yl]methanesulfonamide), VS-4718 (2-[[2-(2-methoxy-4- morpholin-4-
  • FGFR Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an FGFR inhibitor.
  • Exemplary FGFR inhibitors for use in the methods provided herein include, but are not limited to, futibatinib, pemigatinib, ASP5878 (2-[4-[[5-[(2,6-difluoro-3,5- dimethoxyphenyl)methoxy]pyrimidin-2-yl]amino]pyrazol-1-yl]ethanol), AZD4547 (N-[5-[2- (3,5-dimethoxyphenyl)ethyl]-1H-pyrazol-3-yl]-4-[(3S,5R)-3,5-dimethylpiperazin-1- yl]benzamide), debio 1347 ([5-amino-1-(2-methyl-3H-benzimidazol-5-y
  • Glutaminase Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a glutaminase inhibitor.
  • Exemplary glutaminase inhibitors for use in the methods provided herein include, but are not limited to, telaglenastat, IPN60090, and OP 330.
  • IGF-1R Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an IGF-1R inhibitor.
  • IGF-1R inhibitors for use in the methods provided herein include, but are not limited to, cixutumumab, dalotuzumab, linsitinib, ganitumab, robatumumab, BMS- 754807 ((2S)-1-[4-[(5-cyclopropyl-1H-pyrazol-3-yl)amino]pyrrolo[2,1-f][1,2,4]triazin-2-yl]- N-(6-fluoropyridin-3-yl)-2-methylpyrrolidine-2-carboxamide), KW-2450 (N-[5-[[4-(2- hydroxyacetyl)piperazin-1-yl]methyl]-2-[(E)-2-(1H-indazol-3-yl)ethenyl]phenyl]-3- methylthiophene-2-carboxamide), PL225B, AVE1642, and BIIB022.
  • KIF18A Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a KIF18A inhibitor.
  • Exemplary KIF18A inhibitors for use in the methods provided herein include, but are not limited to, the inhibitors disclosed in US 2020/0239441, WO 2020/132649, WO 2020/132651, and WO 2020/132653, each of which is herewith incorporated by reference in its entirety.
  • MCL-1 Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an MCL-1 inhibitor.
  • MEK inhibitors for use in the methods provided herein include, but are not limited to, murizatoclax, tapotoclax, AZD 5991 ((3aR)-5-chloro-2,11,12,24,27,29- hexahydro-2,3,24,33-tetramethyl-22H-9,4,8-(metheniminomethyno)-14,20:26,23-dimetheno- 10H,20H-pyrazolo[4,3-l][2,15,22,18,19]benzoxadithiadiazacyclohexacosine-32-carboxylic acid), MIK 665 (( ⁇ R)- ⁇ -[[(5S)-5-[3-Chloro-2-methyl-4-[2-(4-methyl-1- piperazinyl)ethoxy]phenyl]-6-(4-fluorophenyl)thieno[2,3-d]pyrimidin-4-yl]oxy]-2-[[2-(2-(
  • the MCL-1 inhibitor is murizatoclax. In another embodiment, the MCL-1 inhibitor is tapotoclax.
  • MEK Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is MEK inhibitor.
  • MEK inhibitors for use in the methods provided herein include, but are not limited to, trametinib, cobimetinib, selumetinib, pimasertib, refametinib, PD-325901 (N- [(2R)-2,3-dihydroxypropoxy]-3,4-difluoro-2-(2-fluoro-4-iodoanilino)benzamide), AZD8330 (2-(2-fluoro-4-iodoanilino)-N-(2-hydroxyethoxy)-1,5-dimethyl-6-oxopyridine-3- carboxamide), GDC-0623 (5-(2-fluoro-4-iodoanilino)-N-(2-hydroxyethoxy)imidazo[1,5- a]pyridine-6-carboxamide), RO4987655 (3,4-difluoro-2-(2-fluoro-4-iodoanilino)-N-(2-(2-
  • the MEK inhibitor is trametinib.
  • mTOR Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an mTOR inhibitor.
  • Exemplary mTOR inhibitors for use in the methods provided herein include, but are not limited to, everolimus, rapamycin, zotarolimus (ABT-578), ridaforolimus (deforolimus, MK-8669), sapanisertib, buparlisib, pictilisib, vistusertib, dactolisib, Torin-1 (1-(4-(4- propionylpiperazin-1-yl)-3-(trifluoromethyl)cyclohexyl)-9-(quinolin-3- yl)benzo[h][1,6]naphthyridin-2(1H)-one), GDC-0349 ((S)-1-ethyl-3-(4-(4-(3- methylmorpholino)-7-(oxetan-3-yl)-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidin-2- yl)phenyl)ure
  • the mTOR inhibitor is everolimus.
  • PD-1 Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a PD-1 inhibitor.
  • Exemplary PD-1 inhibitors for use in the methods provided herein include, but are not limited to, pembrolizumab, nivolumab, cemiplimab, spartalizumab (PDR001), camrelizumab (SHR1210), sintilimab (IBI308), tislelizumab (BGB-A317), toripalimab (JS 001), dostarlimab (TSR-042, WBP-285), INCMGA00012 (MGA012), AMP-224, AMP-514, and the anti-PD-1 antibody as described in US 10,640,504 B2 (the “Anti-PD-1 Antibody A,” column 66, line 56 to column 67, line 24 and column 67, lines 54-57), which is incorporated herein by reference.
  • the PD-1 inhibitor is pembrolizumab. In another embodiment the PD-1 inhibitor is the Anti-PD-1 Antibody A.
  • PD-L1 Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a PD-L1 inhibitor.
  • Exemplary PD-L1 inhibitors for use in the methods provided herein include, but are not limited to, atezolizumab, avelumab, durvalumab, ZKAB001, TG-1501, SHR-1316, MSB2311, MDX-1105, KN035, IMC-001, HLX20, FAZ053, CS1001, CK-301, CBT-502, BGB-A333, BCD-135, and A167.
  • the PD-L1 inhibitor is atezolizumab.
  • PI3K Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a PI3K inhibitor.
  • PI3K inhibitors for use in the methods provided herein include, but are not limited to, idelalisib, copanlisib, duvelisib, alpelisib, taselisib, perifosine, buparlisib, umbralisib, pictilisib, dactolisib, voxtalisib, sonolisib, tenalisib, serabelisib, acalisib, CUDC- 907 (N-hydroxy-2-[[2-(6-methoxypyridin-3-yl)-4-morpholin-4-ylthieno[3,2-d]pyrimidin-6- yl]methyl-methylamino]pyrimidine
  • Raf Kinase Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a Raf kinase inhibitor.
  • RAF kinase refers to a member of a mammalian serine/threonine kinases composed of three isoforms (C-Raf, B-Raf and A-Raf) and includes homodimers of each isoform as well as heterodimers between isoforms, e.g., C-Raf/B-Raf heterodimers.
  • Raf kinase inhibitor refers to a compound that is capable of negatively modulating or inhibiting all or a portion of the enzymatic activity of one or more member of the Raf family kinases, or is capable of disrupting Raf homodimer or heterodimer formation to inhibit activity.
  • the Raf kinase inhibitor includes, but is not limited to, encorafenib, sorafenib, lifirafenib, vemurafenib, dabrafenib, PLX-8394 (N-(3-(5-(2- cyclopropylpyrimidin-5-yl)-3a,7a-dihydro-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-2,4- difluorophenyl)-3-fluoropyrrolidine-1-sulfonamide), Raf-709 (N-(2-methyl-5,-morpholino- 6’-((tetrahydro-2H-pyran-4-yl)oxy)-[3,3'-bipyridin]-5-yl)-3-(trifluoromethyl)benzamide), LXH254 (N-(3-(2-(2-hydroxyethoxy)-6- morpholinopyridin-4-yl)
  • the Raf kinase inhibitor is encorafenib. In one embodiment, the Raf kinase inhibitor is sorafenib. In one embodiment, the Raf kinase inhibitor is lifirafenib.
  • SHP2 Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a SHP2 inhibitor.
  • Exemplary SHP2 inhibitors for use in the methods provided herein include, but are not limited to, SHP-099 (6-(4-amino-4-methylpiperidin-1-yl)-3-(2,3-dichlorophenyl)pyrazin- 2-amine dihydrochloride), RMC-4550 ([3-[(3S,4S)-4-amino-3-methyl-2-oxa-8- azaspiro[4.5]decan-8-yl]-6-(2,3-dichlorophenyl)-5-methylpyrazin-2-yl]methanol), TNO155, (3S,4S)-8-[6-amino-5-(2-amino-3-chloropyridin-4-yl)sulfanylpyrazin-2-yl]-3-methyl-2-oxa- 8-azaspiro[4.5]decan-4-amine), and RMC-4630 (Revolution Medicine).
  • the SHP inhibitor for use in the methods provided herein is RMC-4630 (Revolution Medicine).
  • exemplary SHP2 inhibitors for use in the methods provided herein include, but are not limited to, 3-[(1R,3R)-1-amino-3-methoxy-8-azaspiro[4.5]dec-8- yl]-6-(2,3-dichlorophenyl)-5-methyl-2-pyrazinemethanol (CAS 2172651-08-8), 3-[(3S,4S)-4- amino-3-methyl-2-oxa-8-azaspiro[4.5]dec-8-yl]-6-[(2,3-dichlorophenyl)thio]-5-methyl-2- pyrazinemethanol (CAS 2172652-13-8), 3-[(3S,4S)-4-amino-3-methyl-2-oxa-8- azaspiro[4.5]dec-8-yl]-6-[[3-chloro-2-(3-hydroxy-1-azet)
  • exemplary SHP2 inhibitors for use in the methods provided herein include, but are not limited to, 1-[5-(2,3-dichlorophenyl)-6-methylimidazo[1,5- a]pyrazin-8-yl]-4-methyl-4-piperidinamine (CAS 2240981-75-1), (1R)-8-[5-(2,3- dichlorophenyl)-6-methylimidazo[1,5-a]pyrazin-8-yl]-8-azaspiro[4.5]decan-1-amine (CAS 2240981-78-4), (3S,4S)-8-[7-(2,3-dichlorophenyl)-6-methylpyrazolo[1,5-a]pyrazin-4-yl]-3- methyl-2-oxa-8-azaspiro[4.5]decan-4-amine (CAS 2240982-45-8), (3S,4S)-8-[7-[(2-amino-3- chloro-4-pyridinyl)thio]pyra
  • the SHP inhibitor for use in the methods provided herein is (1R)- 8-[5-(2,3-dichlorophenyl)-6-methylimidazo[1,5-a]pyrazin-8-yl]-8-azaspiro[4.5]decan-1- amine (CAS 2240981-78-4).
  • exemplary SHP2 inhibitors for use in the methods provided herein include, but are not limited to 3-[(1R)-1-amino-8-azaspiro[4.5]dec-8-yl]-6-(2,3- dichlorophenyl)-5-hydroxy-2-pyridinemethanol (CAS 2238840-54-3), 3-[(1R)-1-amino-8- azaspiro[4.5]dec-8-yl]-6-[(2,3-dichlorophenyl)thio]-5-hydroxy-2-pyridinemethanol (CAS 2238840-56-5), 5-[(1R)-1-amino-8-azaspiro[4.5]dec-8-yl]-2-(2,3-dichlorophenyl)-3-pyridinol (CAS 2238840-58-7), 3-[(1R)-1-amino-8-azaspiro[4.5]dec-8-yl]-6-(2,3-dichlorophenyl)-5- methyl-2-pyridinem
  • the SHP inhibitor for use in the methods provided herein is 3- [(1R)-1-amino-8-azaspiro[4.5]dec-8-yl]-6-[(2,3-dichlorophenyl)thio]-5-hydroxy-2- pyridinemethanol (CAS 2238840-56-5).
  • the SHP2 inhibitor for use in the methods provided herein is an inhibitor disclosed in US 10,590,090 B2, US 2020/017517 A1, US 2020/017511 A1, or WO 2019/075265 A1, each of which is herewith incorporated by reference in its entirety.
  • SOS1 Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is an SOS1 inhibitor.
  • exemplary SOS1 inhibitors for use in the methods provided herein include, but are not limited to, BI 3406 (N-[(1R)-1-[3-amino-5-(trifluoromethyl)phenyl]ethyl]-7-methoxy-2- methyl-6-[(3S)-oxolan-3-yl]oxyquinazolin-4-amine), and BI 1701963.
  • Src Kinase Inhibitors Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is a Src kinase inhibitor.
  • the term “Src kinase” as used herein refers to a member of a mammalian nonreceptor tyrosine kinase family including: Src, Yes, Fyn, and Fgr (SrcA subfamily); Lck, Hck, Blk, and Lyn (SrcB subfamily), and Frk subfamily.
  • the Src kinase inhibitor is dasatinib. In one embodiment, the Src kinase inhibitor is saracatinib. In one embodiment, the Src kinase inhibitor is ponatinib. In one embodiment, the Src kinase inhibitor is vandetanib. In one embodiment, the Src kinase inhibitor is KX-01.
  • Chemotherapeutic Agents Provided herein is the method according to anyone of Embodiments 331-338, which further comprises simultaneous, separate, or sequential administration of an effective amount of a second compound, wherein the second compound is one or more chemotherapeutic agent.
  • chemotherapeutic agents for use in the methods provided herein include, but are not limited to, leucovorin calcium (calcium folinate), 5-fluorouracil, irinotecan, oxaliplatin, cisplatin, carboplatin, pemetrexed, docetaxel, paclitaxel, gemcitabine, vinorelbine, chlorambucil, cyclophosphamide, and methotrexate.
  • Stereoisomers may contain, for example, double bonds, one or more asymmetric carbon atoms, and bonds with a hindered rotation, and therefore, may exist as stereoisomers, such as double-bond isomers (i.e., geometric isomers (E/Z)), enantiomers, diastereomers, and atropoisomers.
  • double-bond isomers i.e., geometric isomers (E/Z)
  • enantiomers e.e., diastereomers, and atropoisomers.
  • the scope of the instant disclosure is to be understood to encompass all possible stereoisomers of the illustrated compounds, including the stereoisomerically pure form (for example, geometrically pure, enantiomerically pure, diastereomerically pure, and atropoisomerically pure) and stereoisomeric mixtures (for example, mixtures of geometric isomers, enantiomers, diastereomers, and atropoisomers, or mixture of any of the foregoing) of any chemical structures disclosed herein (in whole or in part), unless the stereochemistry is specifically identified.
  • stereoisomerically pure form for example, geometrically pure, enantiomerically pure, diastereomerically pure, and atropoisomerically pure
  • stereoisomeric mixtures for example, mixtures of geometric isomers, enantiomers, diastereomers, and atropoisomers, or mixture of any of the foregoing
  • stereochemistry of a structure or a portion of a structure is not indicated with, for example, bold or dashed lines, the structure or portion of the structure is to be interpreted as encompassing all stereoisomers of it. If the stereochemistry of a structure or a portion of a structure is indicated with, for example, bold or dashed lines, the structure or portion of the structure is to be interpreted as encompassing only the stereoisomer indicated.
  • a bond drawn with a wavy line indicates that both stereoisomers are encompassed. This is not to be confused with a wavy line drawn perpendicular to a bond which indicates the point of attachment of a group to the rest of the molecule.
  • stereoisomer or “stereoisomerically pure” compound as used herein refers to one stereoisomer (for example, geometric isomer, enantiomer, diastereomer and atropoisomer) of a compound that is substantially free of other stereoisomers of that compound.
  • a stereoisomerically pure compound having one chiral center will be substantially free of the mirror image enantiomer of the compound and a stereoisomerically pure compound having two chiral centers will be substantially free of other enantiomers or diastereomers of the compound.
  • a typical stereoisomerically pure compound comprises greater than about 80% by weight of one stereoisomer of the compound and equal or less than about 20% by weight of other stereoisomers of the compound, greater than about 90% by weight of one stereoisomer of the compound and equal or less than about 10% by weight of the other stereoisomers of the compound, greater than about 95% by weight of one stereoisomer of the compound and equal or less than about 5% by weight of the other stereoisomers of the compound, or greater than about 97% by weight of one stereoisomer of the compound and equal or less than about 3% by weight of the other stereoisomers of the compound.
  • This disclosure also encompasses the pharmaceutical compositions comprising stereoisomerically pure forms and the use of stereoisomerically pure forms of any compounds disclosed herein.
  • this disclosure also encompasses pharmaceutical compositions comprising mixtures of stereoisomers of any compounds disclosed herein and the use of said pharmaceutical compositions or mixtures of stereoisomers. These stereoisomers or mixtures thereof may be synthesized in accordance with methods well known in the art and methods disclosed herein. Mixtures of stereoisomers may be resolved using standard techniques, such as chiral columns or chiral resolving agents. Further, this disclosure encompasses pharmaceutical compositions comprising mixtures of any of the compounds disclosed herein and one or more other active agents disclosed herein.
  • isotopes suitable for inclusion in the compounds disclosed herein include isotopes of hydrogen, such as 2 H and 3 H, carbon, such as 11 C, 13 C and 14 C, chlorine, such as 36 CI, fluorine, such as 18 F, iodine, such as 123 I and 125 I, nitrogen, such as 13 N and 15 N, oxygen, such as 15 O, 17 O and 18 O, phosphorus, such as 32 P, and sulphur, such as 35 S.
  • isotopically-labelled compounds of Formula I for example, those incorporating a radioactive isotope, are useful in drug and/or substrate tissue distribution studies.
  • radioactive isotopes tritium ( 3 H) and carbon-14 ( 14 C) are particularly useful for this purpose in view of their ease of incorporation and ready means of detection.
  • substitution with isotopes such as deuterium ( 2 H or D) may afford certain therapeutic advantages resulting from greater metabolic stability, for example, increased in vivo half-life or reduced dosage requirements, and hence may be advantageous in some circumstances.
  • substitution with positron emitting isotopes, such as 11 C, 18 F, 15 O and 13 N can be useful in Positron Emission Topography (PET) studies, for example, for examining target occupancy.
  • PET Positron Emission Topography
  • Isotopically- labelled compounds of the compounds disclosed herein can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described in the accompanying General Synthetic Schemes and Examples using an appropriate isotopically-labelled reagent in place of the non-labelled reagent previously employed.
  • Solvates As discussed above, the compounds disclosed herein and the stereoisomers, tautomers, and isotopically-labelled forms thereof or a pharmaceutically acceptable salt of any of the foregoing may exist in solvated or unsolvated forms.
  • solvate refers to a molecular complex comprising a compound or a pharmaceutically acceptable salt thereof as described herein and a stoichiometric or non-stoichiometric amount of one or more pharmaceutically acceptable solvent molecules. If the solvent is water, the solvate is referred to as a “hydrate.” Accordingly, the scope of the instant disclosure is to be understood to encompass all solvents of the compounds disclosed herein and the stereoisomers, tautomers and isotopically-labelled forms thereof or a pharmaceutically acceptable salt of any of the foregoing. Miscellaneous Definitions This section will define additional terms used to describe the scope of the compounds, compositions and uses disclosed herein.
  • aryl refers to an aromatic hydrocarbon group having 6-20 carbon atoms in the ring portion. Typically, aryl is monocyclic, bicyclic or tricyclic aryl having 6-20 carbon atoms. Furthermore, the term “aryl” as used herein, refers to an aromatic substituent which can be a single aromatic ring, or multiple aromatic rings that are fused together.
  • Non-limiting examples include phenyl, naphthyl or tetrahydronaphthyl, each of which may optionally be substituted with 1-4 substituents, such as alkyl, trifluoromethyl, cycloalkyl, halogen, hydroxy, alkoxy, acyl, alkyl-C(O)-O-, aryl-O-, heteroaryl-O-, amino, thiol, alkyl-S-, aryl-S--- nitro, cyano, carboxy, alkyl-O-C(O)--, carbamoyl, alkyl-S(O)-, sulfonyl, sulfonamido, phenyl, and heterocycloalkyl.
  • substituents such as alkyl, trifluoromethyl, cycloalkyl, halogen, hydroxy, alkoxy, acyl, alkyl-C(O)-O-, aryl-O-,
  • C 1-4 alkyl and “C 1-6 alkyl” as used herein refer to a straight or branched chain hydrocarbon containing from 1 to 4, and 1 to 6 carbon atoms, respectively.
  • Representative examples of C 1-4 alkyl or C 1-6 alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, pentyl and hexyl.
  • C 1-4 alkylene and “C 1-6 alkylene” refer to a straight or branched divalent alkyl group as defined herein containing 1 to 4, and 1 to 6 carbon atoms, respectively.
  • alkylene examples include, but are not limited to, methylene, ethylene, n- propylene, iso-propylene, n-butylene, sec-butylene, iso-butylene, tert-butylene, n-pentylene, isopentylene, neopentylene, n-hexylene and the like.
  • C 2-4 alkenyl refers to a saturated hydrocarbon containing 2 to 4 carbon atoms having at least one carbon-carbon double bond. Alkenyl groups include both straight and branched moieties.
  • C 2-4 alkenyl include, but are not limited to, 1-propenyl, 2-propenyl, 2-methyl-2-propenyl, and butenyl.
  • C 2-4 alkynyl refers to a saturated hydrocarbon containing 2 to 4 carbon atoms having at least one carbon-carbon triple bond. The term includes both straight and branched moieties.
  • Representative examples of C 3-6 alkynyl include, but are not limited to, ethynyl, 1 -propynyl, 2-propynyl, 2-butynyl and 3-butynyl.
  • C 1-4 alkoxy or “C 1-6 alkoxy” as used herein refers to –OR # , wherein R # represents a C 1-4 alkyl group or C 1-6 alkyl group, respectively, as defined herein.
  • Representative examples of C 1-4 alkoxy include, but are not limited to, methoxy, ethoxy, propoxy, iso-propoxy, and butoxy.
  • Representative examples of C 1-6 alkoxy include, but are not limited to, ethoxy, propoxy, iso-propoxy, and butoxy.
  • C 3-8 cycloalkyl refers to a saturated carbocyclic molecule wherein the cyclic framework has 3 to 8 carbons.
  • C 3-8 cycloalkyl include, but are not limited to, cyclopropyl and cyclobutyl.
  • deutero as used herein as a prefix to another term for a chemical group refers to a modification of the chemical group, wherein one or more hydrogen atoms are substituted with deuterium (“D” or “ 2 H”).
  • D deuterium
  • C 1-4 deuteroalkyl refers to a C 1-4 alkyl as defined herein, wherein one or more hydrogen atoms are substituted with D.
  • C 1-4 deuteroalkyl include, but are not limited to, -CH 2 D, -CHD 2 , - CD 3 , -CH 2 CD 3 , -CDHCD 3 , -CD 2 CD 3 , -CH(CD 3 ) 2 , -CD(CHD 2 ) 2 , and -CH(CH 2 D)(CD 3 ).
  • halogen refers to –F, -CI, -Br, or -I.
  • halo as used herein as a prefix to another term for a chemical group refers to a modification of the chemical group, wherein one or more hydrogen atoms are substituted with a halogen as defined herein.
  • C 1-4 haloalkyl refers to a C 1-4 alkyl as defined herein, wherein one or more hydrogen atoms are substituted with a halogen.
  • Representative examples of C 1- 4 haloalkyl include, but are not limited to, -CH 2 F, -CHF 2 , -CF 3 , -CHFCl, -CH 2 CF 3 , -CFHCF 3 , -CF 2 CF 3 , -CH(CF 3 ) 2 , -CF(CHF 2 ) 2 , and -CH(CH 2 F)(CF 3 ).
  • heteroaryl refers to a 5-20 membered monocyclic- or bicyclic- or tricyclic-aromatic ring system, having 1 to 8 heteroatoms selected from N, O and S.
  • the heteroaryl is a 5-10 membered ring system (e.g., 5-7 membered monocycle, an 8-10 membered bicycle or a 11-14 membered tricycle) or a 5-7 membered ring system.
  • Exemplary monocyclic heteroaryl groups include 2- or 3-thienyl, 2- or 3-furyl, 2- or 3-pyrrolyl, 2-, 4-, or 5-imidazolyl, 3-, 4-, or 5-pyrazolyl, 2-, 4-, or 5-thiazolyl, 3-, 4-, or 5-isothiazolyl, 2-, 4-, or 5-oxazolyl, 3-, 4-, or 5-isoxazolyl, 3- or 5-1,2,4-triazolyl, 4- or 5-1,2,3-triazolyl, tetrazolyl, 2-, 3-, or 4-pyridyl, 3- or 4-pyridazinyl, 3-, 4-, or 5-pyrazinyl, 2-pyrazinyl, and 2-, 4-, and 5-pyrimidinyl.
  • Exemplary bicyclic heteroaryl groups include 1-, 3-, 4-, 5-, 6-, 7-, or 8-isoquinolinyl, 2-, 3-, 4-, 5-, 6-, 7-, or 8-quinolinyl, 1-, 3-, 4-, 5-, 6-, 7-, or 8-isoquinolinyl, 1-, 2-, 4-, 5-, 6-, 7-, or 8-benzimidazolyl and 1-, 2-, 3-, 4-, 5-, 6-, 7-, or 8- indolyl.
  • heteroaryl also refers to a group in which a heteroaromatic ring is fused to one or more aryl, cycloaliphatic, or heterocycloalkyl rings.
  • heterocycle refers to a saturated or unsaturated non-aromatic ring or ring system, e.g., which is a 4-, 5-, 6-, or 7- membered monocyclic, 7-, 8-, 9-, 10-, 11-, or 12-membered bicyclic or 10-, 11-, 12-, 13-, 14- or 15-membered tricyclic ring system and contains at least one heteroatom selected from O, S and N, where the N and S can also optionally be oxidized to various oxidation states.
  • the heterocyclic group can be attached at a heteroatom or a carbon atom.
  • the heterocycloalkyl can include fused or bridged rings as well as spirocyclic rings.
  • heterocycles include tetrahydrofuran, dihydrofuran, 1, 4-dioxane, morpholine, 1,4-dithiane, piperazine, piperidine, 1,3-dioxolane, imidazolidine, imidazoline, pyrroline, pyrrolidine, tetrahydropyran, dihydropyran, oxathiolane, dithiolane, 1,3-dioxane, 1,3-dithiane, oxathiane, thiomorpholine, azetidine, thiazolidine, morpholine, and the like.
  • pharmaceutically acceptable refers to generally recognized for use in subjects, particularly in humans.
  • pharmaceutically acceptable salt refers to a salt of a compound that is pharmaceutically acceptable and that possesses the desired pharmacological activity of the parent compound.
  • Such salts include: (1) acid addition salts, formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; or formed with organic acids such as acetic acid, propionic acid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, 3-(4-hydroxybenzoyl) benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, and the like; or (2) salts formed when an acidic proton present in the parent compound either is replaced by a metal ion, for example, an alkali metal ion, an alkaline earth ion, or an aluminum ion; or coordinates with an organic base such as ethanolamine, diethanolamine, triethanolamine, N-
  • excipient refers to a broad range of ingredients that may be combined with a compound or salt disclosed herein to prepare a pharmaceutical composition or formulation.
  • excipients include, but are not limited to, diluents, colorants, vehicles, anti-adherants, glidants, disintegrants, flavoring agents, coatings, binders, sweeteners, lubricants, sorbents, preservatives, and the like.
  • subject refers to humans and mammals, including, but not limited to, primates, cows, sheep, goats, horses, dogs, cats, rabbits, rats, and mice. In one embodiment the subject is a human.
  • therapeutically effective amount refers to that amount of a compound disclosed herein that will elicit the biological or medical response of a tissue, a system, or subject that is being sought by a researcher, veterinarian, medical doctor or other clinician.
  • GENERAL SYNTHETIC PROCEDURES The compounds provided herein can be synthesized according to the procedures described in this and the following sections.
  • the compounds disclosed herein may also be synthesized by alternate routes utilizing alternative synthetic strategies, as appreciated by persons of ordinary skill in the art. It should be appreciated that the general synthetic procedures and specific examples provided herein are illustrative only and should not be construed as limiting the scope of the present disclosure in any manner.
  • the compounds of Formula I can be synthesized according to the following schemes. Any variables used in the following schemes are the variables as defined for Formula I, unless otherwise noted. All starting materials are either commercially available, for example, from Merck Sigma-Aldrich Inc., Fluorochem Ltd, and Enamine Ltd. or known in the art and may be synthesized by employing known procedures using ordinary skill.
  • step A compound (I-1) is treated with an aliphatic alcohol, such as benzyl alcohol, and a base, such as Hunig’s base, or metal alkoxide, such as potassium tert-butoxide, in a solvent such as 1,4-dioxane to give compound (I-2).
  • an aliphatic alcohol such as benzyl alcohol
  • a base such as Hunig’s base
  • metal alkoxide such as potassium tert-butoxide
  • step B compound (I-2) undergoes S N Ar reaction with a nucleophile having the formula R 1 -L-H in a solvent such as acetonitrile, in the presence of a base such as Hunig’s base, to give compound (I-3).
  • step C compound (I-3) is coupled with an organometallic reagent or a boronic acid (ester) to provide compound (I-4).
  • This coupling reaction proceeds in a solvent or mixture of solvents such as 1,4-dioxane and water, and a catalyst such as cataCXium A Pd G3, with or without a base such as potassium phosphate.
  • step D compound (I-4) is treated with a suitable set of reagents, such as Pd/C with H 2 to remove the alkyl group R, giving compound (I-5).
  • Step E compound (I-5) is treated with an optionally substituted cyclic amine in the presence of coupling reagent such as HATU, and a base such as Hunig’s base, in a solvent such as DMA to give compounds of Formula (I).
  • the species R 3 will contain protecting group(s), which can be removed in step D or after step E in the synthetic sequence.
  • compound (I-1) is treated with sodium thiomethoxide in a solvent such as tetrahydrofuran to give compound (I-6).
  • step B compound (I-6) undergoes SNAr reaction with a nucleophile having the formula R 1 -L-H in a solvent such as acetonitrile in the presence of a base such as Hunig’s base to give compound (I-7).
  • step C compound (I-7) is coupled with an organometallic reagent or a boronic acid (ester) to provide compound (I-8).
  • This coupling reaction proceeds in a solvent or mixture of solvents such as 1,4-dioxane and water, and a catalyst such as cataCXium A Pd G3, with or without a base such as potassium phosphate.
  • step D compound (I-8) is coupled with an optionally substituted cyclic amine in the presence of a palladium catalyst, such as Pd(PPh 3 ) 4 , a copper catalyst, such as CuTC, in a solvent such as 1,4-dioxane, to give compounds of formula (I).
  • a palladium catalyst such as Pd(PPh 3 ) 4
  • a copper catalyst such as CuTC
  • a solvent such as 1,4-dioxane
  • Scheme III Compounds of Formula (I) can also be prepared according to Scheme III.
  • step A compound (I-8) is treated with sulfuryl chloride in a solvent such as dichloromethane to give compound (I-9).
  • step B compound (I-9) undergoes S N Ar reaction with an optionally substituted cyclic amine in a solvent such as acetonitrile in the presence of a base such as Hunig’s base to give compounds of formula (I).
  • the species R 3 will contain protecting group(s), which can be removed after step B in the synthetic sequence.
  • step A compound (1) undergoes SNAr reaction with an optionally substituted cyclic amine in a solvent such as dichloromethane and in the presence of a base such as Hunig’s base to give compound (I-10).
  • step B compound (I-10) undergoes S N Ar reaction with a nucleophile having the formula R 1 -L-H in a solvent such as acetonitrile, in the presence of a base such as Hunig’s base to give compound (I-11).
  • step C compound (I-11) is coupled with an organometallic reagent or a boronic acid (ester) to provide compounds of formula (I).
  • Preparative HPLC Method where indicated, the compounds described herein were purified via reverse phase HPLC using Waters FractionLynx or Gilson semi-preparative HPLC-MS system utilizing one of the following two HPLC columns: (a) Phenomenex Gemini column (5 micron, C18, 150 x 30 mm) or (b) Waters X-select CSH column (5 micron, C18, 100 x 30 mm). A typical run through the instrument included: eluting at 45 mL/min with a linear gradient of 10% (v/v) to 100% MeCN (0.1% v/v formic acid) in water (0.1% formic acid) over 10 minutes; conditions can be varied to achieve optimal separations.
  • a microwave vial was charged with methyl 2-(2-bromo-3,4-difluorophenyl)acetate (1.62 g, 6.11 mmol), trifluorotoluene (15 mL), tributyl(1-ethoxyvinyl)stannane (4.41 g, 12.22 mmol), and trans- dichlorobis(triphenyl-phosphine)palladium (II) (0.86 g, 1.22 mmol).
  • the vial was purged with nitrogen for 2 min, sealed, and placed in a microwave reactor for 12 h at 150 o C. Upon completion, the mixture was filtered through a celite / silica plug and concentrated.
  • Step 3 7,8-Difluoronaphthalene-1,3-diol.
  • methyl 2-(2-acetyl-3,4-difluorophenyl)acetate (1.21 g, 5.30 mmol)
  • KOtBu (1.79 g, 15.91 mmol
  • THF 40 mL
  • Step 5 7,8-Difluoro-3-((triisopropylsilyl)oxy)naphthalen-1-yl trifluoromethanesulfonate.
  • 78-difluoro-3- ((triisopropylsilyl)oxy)naphthalen-1-ol (0.88 g, 2.50 mmol)
  • DIPEA 1.31 mL, 7.51 mmol
  • DCM 25 mL
  • Tf 2 O (1 M in DCM, 2.76 mL, 2.76 mmol
  • Step 6 ((5,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2- yl)naphthalen-2-yl)oxy)triisopropylsilane.
  • a 100-mL round-bottomed flask was charged - 128 - with 7,8-difluoro-3-((triisopropylsilyl)oxy)naphthalen-1-yl trifluoromethanesulfonate (1.21 g, 2.50 mmol), bis(pinacalato)diboron (1.27 g, 4.99 mmol), potassium acetate (0.86 g, 8.74 mmol), 1,1'-bis(diphenylphosphino)ferrocene-palladium dichloride (0.37 g, 0.499 mmol) and toluene (25 mL).
  • Step 1 7-Fluoro-8-((triisopropylsilyl)ethynyl)naphthalen-1-ol.
  • a pressure relief vial was charged with potassium acetate (1.21 g, 12.3 mmol, Sigma Aldrich), 7-fluoro-1- naphthol (1.00 g, 6.17 mmol, Enamine), dichloro(p-cymene)ruthenium(II)dimer (0.38 g, 0.62 mmol, Alfa Aesar) and then purged with nitrogen for 5 min.
  • Step 3 8-Ethyl-7-fluoronaphthalen-1-ol.
  • a scintillation vial was charged with 7- fluoro-8-((triisopropylsilyl)ethynyl)naphthalen-1-yl pivalate (1.13 g, 2.65 mmol) and dissolved in DMF (12 mL).
  • Cesium fluoride (4.02 g, 26.5 mmol, Sigma-Aldrich Corporation) was added and the mixture stirred at rt for 30 minutes. Water (100 mL) was added and the aqueous phase extracted with EtOAc (2 ⁇ 20 mL).
  • TEA 0.28 g, 0.39 mL, 2.76 mmol, Sigma-Aldrich Corporation
  • a 1 M Tf 2 O solution (2.02 mL, 2.02 mmol, Sigma-Aldrich Corporation).
  • the mixture was stirred at rt for 20 minutes and poured into ice water (20 mL).
  • the aqueous phase was extracted with DCM (2 x 10 mL), the combined organic layers were dried over Na 2 SO 4 and volatiles were removed in vacuo.
  • the crude mixture was purified by column chromatography on silica gel, eluting using a gradient of 0-5% EtOAc in heptane to yield 8- ethyl-7-fluoronaphthalen-1-yl trifluoromethanesulfonate (0.47 g, 1.47 mmol, 80 % yield) as colorless oil.
  • Potassium acetate (0.43 g, 4.38 mmol, Sigma-Aldrich Corporation) was placed in a pressure relief vial and dried under vacuum. Then, 8-ethyl-7-fluoronaphthalen-1- yl trifluoromethanesulfonate (0.47 g, 1.46 mmol), bis(pinacalato)diboron (0.74 g, 2.92 mmol, Combi-Blocks Inc.) and [1,1'-bis(diphenylphosphino)ferrocene] dichloropalladium(II) (0.11 g, 0.15 mmol, Sigma-Aldrich Corporation) were added and the mixture stirred at 90 °C for 3 h and then at rt for 12 h.
  • Step 1 4-(Benzyloxy)-2,7-dichloro-8-fluoropyrido[4,3-d]pyrimidine.
  • a 250-mL round-bottom flask charged with activated 3 ⁇ molecular sieves was added 1,4-dioxane (48 mL), DIPEA (9.22 g, 12.5 mL, 71.3 mmol), benzyl alcohol (3.86 g, 3.7 mL, 35.7 mmol) and 2,4,7-trichloro-8-fluoropyrido[4,3-d]pyrimidine (6.00 g, 23.8 mmol). The mixture was stirred at 85 °C for 2 h.
  • Step 2 4-(Benzyloxy)-7-chloro-8-fluoro-2-(((2S,7aR)-2-fluorotetrahydro-1H- pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidine.
  • Step 3 4-(Benzyloxy)-7-(8-ethyl-7-fluoro-3-(methoxymethoxy)naphthalen-1-yl)- 8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidine.
  • reaction mixture was stirred at 70 °C for 2 h.
  • the reaction mixture was purified by column chromatography on silica gel, eluting with 0-50% 3:1 EtOAc/EtOH blend in heptane with 2% triethylamine additive to yield 4-(benzyloxy)-7-(8-ethyl-7-fluoro-3- (methoxymethoxy)naphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin- 7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidine (2.42 g, 3.75 mmol, 65 % yield).
  • Step 4 7-(8-Ethyl-7-fluoro-3-(methoxymethoxy)naphthalen-1-yl)-8-fluoro-2- (((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidin-4-ol.
  • Step 3 4-(tert-Butoxy)-7-(8-ethyl-7-fluoro-3-(methoxymethoxy)naphthalen-1-yl)- 8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidine.
  • Step 4 7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-ol.
  • Step 2 7-Chloro-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin- 7a(5H)-yl)methoxy)-4-(methylthio)pyrido[4,3-d]pyrimidine.
  • Step 3 7-(8-Ethyl-7-fluoro-3-(methoxymethoxy)naphthalen-1-yl)-8-fluoro-2- (((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)-4- (methylthio)pyrido[4,3-d]pyrimidine.
  • reaction was stirred at 85 °C for 1.5 h.
  • the reaction mixture was concentrated under reduced pressure and purified by column chromatography twice, eluting with first a gradient of 0-50% (20% MeOH in DCM) in DCM, then 0-50% 3:1 EtOAc/EtOH in heptane with 2% triethylamine additive to afford 7-(8-ethyl- 7-fluoro-3-(methoxymethoxy)naphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H- pyrrolizin-7a(5H)-yl)methoxy)-4-(methylthio)pyrido[4,3-d]pyrimidine (1.50 g, 2.57 mmol, 42 % yield) as yellow solid.
  • ammonium hydroxide (4.20 g, 4.6 mL, 0.12 mol, Fisher Scientific) was added and the reaction was stirred at the same temperature overnight. The organic solvent was removed under reduced pressure. The remaining solution was then diluted with EtOAc (10 mL) and the organic layer was washed with 10% aq. citric acid (10 mL), saturated aqueous sodium bicarbonate (10 mL), and brine (10 mL).
  • Benzyl 3-hydroxy-3-methylazepane-1-carboxylate (0.24 g) was purified via SFC using a Chiralpak IG, 21 ⁇ 250 mm 5 ⁇ m, column with a mobile phase of 20% methanol with 0.2% triethylamine using a flowrate of 80 mL/min to generate 89 mg of peak 1 with an ee of >99% and 91 mg of peak 2 with an ee of >99%.
  • Step 3 3-Methylazepan-3-ol hydrochloride. Benzyl 3-hydroxy-3-methylazepane- 1-carboxylate (89 mg, 0.34 mmol, Peak 1) was dissolved in ethanol (1.7 mL).
  • Step 2 tert-Butyl 6-cyano-3-azabicyclo[3.2.2]nonane-3-carboxylate.
  • a stirring solution of tert-butyl 6-carbamoyl-3-azabicyclo[3.2.2]nonane-3-carboxylate (0.13 g, 0.47 mmol) in pyridine (1.2 mL) was added 1H-imidazole (63 mg, 0.93 mmol, Sigma Aldrich).
  • the resultant mixture was cooled to 0 °C, and phosphorous oxychloride (0.29 g, 0.17 mL, 1.86 mmol, Sigma-Aldrich Corporation) was added slowly dropwise and the mixture kept at the same temperature.
  • Step 3 8-Oxa-3-azabicyclo[3.2.1]octane-6-carbonitrile hydrochloride.
  • tert-Butyl 6-cyano-3-azabicyclo[3.2.2]nonane-3-carboxylate (94 mg, 0.38 mmol) was then dissolved in MeCN (3.5 mL) and HCl in 1,4-dioxane (4 M, 0.47 mL, 1.86 mmol, Sigma-Aldrich Corporation) was added.
  • Step 1 (E)-5-Chloro-6-fluoro-3,4-dihydronaphthalen-1(2H)-one oxime.
  • 5-chloro-6-fluoro-3,4-dihydronaphthalen-1(2H)-one (0.40 kg, 2.01 mol) in EtOH (2.4 L) and H 2 O (0.8 L) was added NaOAc (0.25 kg, 3.02 mol) and NH 2 OH•HCl (0.21 kg, 3.02 mol).
  • the reaction was stirred at 25 °C for 12 h.
  • Four reactions were carried out in parallel, and were combined for work up.
  • the mixture was poured into ice, and then extracted with EtOAc (3 L ⁇ 3).
  • Step 4 5-Bromo-6-chloro-7-fluoronaphtho[1,2-d][1,2,3]oxadiazole.
  • Step 6 8-Bromo-1-chloro-2-fluoro-6-(methoxymethoxy)naphthalene.
  • a solution of 4-bromo-5-chloro-6-fluoronaphthalen-2-ol (55 g, 0.20 mol) and DIPEA (77 g, 0.10 L, 0.60 mol) in DCM (0.33 L) was cooled to 0 °C, then MOMCl (32 g, 30 mL, 0.40 mol) was added to the mixture dropwise.
  • the solution was warmed to 25 °C and stirred for 12 h.
  • the reaction mixture was quenched by addition saturated NaHCO 3 (aq.
  • Step 7 2-(8-Chloro-7-fluoro-3-(methoxymethoxy)naphthalen-1-yl)-4,4,5,5- tetramethyl-1,3,2-dioxaborolane.
  • Step 3 (R)-1-(7-Chloro-8-fluoro-2-(methylthio)pyrido[4,3-d]pyrimidin-4-yl)-3- methylpiperidin-3-ol.
  • Step 5 (3R)-1-(7-(8-Ethyl-7-fluoro-3-(methoxymethoxy)naphthalen-1-yl)-8- fluoro-2-(methylsulfinyl)pyrido[4,3-d]pyrimidin-4-yl)-3-methylpiperidin-3-ol.
  • the product fractions were combined, frozen, and lyophilized; the residue was redissolved in ethyl acetate, washed with aqueous potassium carbonate, and concentrated to provide 1- benzyl-3-(methyl-d3)piperidin-3-ol (1.6 g, 7.44 mmol, 56 % yield) as colorless oil.
  • the racemic mixture was purified via SFC using a Chiralpak AD (21 x 250 mm 5 ⁇ m) column with a mobile phase of 10% methanol with 2% diethylamine using a flowrate of 120 mL/min, to provide two products.
  • the first-eluting product (242 mg, 1.16 mmol, 8.7 % yield, ee: >99 %) was assiged the R stereochemistry.
  • the reaction mixture was then diluted with saturated NH 4 Cl solution (10 mL) and extracted with EtOAc (2 ⁇ 10 mL). The organic extract was washed with saturated NaCl solution ( 20 mL) and dried over MgSO 4 . The solution was filtered and concentrated in vacuo to give the crude material, which was absorbed onto a plug of silica gel and purified by column chromatography on silica gel, eluting with a gradient of 0 - 50% EtOAc in heptane, to provide 8-bromo-1-ethyl-1,2,3,4-tetrahydronaphthalen-1-ol (0.71 g, 2.78 mmol, 87 % yield) as yellow oil.
  • Step 2.8-Bromo-1-ethyl-1,2,3,4-tetrahydronaphthalene To a 25-mL round- bottomed flask was added 8-bromo-1-ethyl-1,2,3,4-tetrahydronaphthalen-1-ol (0.48 g, 1.88 mmol ) in DCM (7.5 mL). After cooling to -30 °C, triethylsilane (1.09 g, 9.41 mmol,) was added, followed by dropwise addition of TFA (0.64 g, 0.44 mL, 5.6 mmol).
  • the reaction mixture was stirred for 3 h while slowly warming to rt.
  • the reaction mixture was diluted with water (15 mL) and extracted with EtOAc ( 2 ⁇ 15 mL).
  • the organic extract was washed with saturated NaCl solution (15 mL) and dried over MgSO 4 .
  • the solution was filtered and concentrated in vacuo to give the crude material, which was absorbed onto a plug of silica gel and purified by column chromatography on silica gel, eluting with a gradient of 0 - 20% EtOAc in heptane, to provide 8-bromo-1-ethyl-1,2,3,4-tetrahydronaphthalene (0.39 g, 1.63 mmol, 87 % yield) as colorless oil.
  • the reaction was purged with nitrogen for 5 min and then stirred at 65 °C for 3 h.
  • the reaction mixture was concentrated and the crude material was absorbed onto a plug of silica gel and purified by column chromatography on silica gel, eluting with a gradient of 0 - 70% EtOAc in hexane, to provide 2-(4-bromo-5-ethyl-5,6,7,8- tetrahydronaphthalen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.20 g, 0.55 mmol, 62 % yield) as colorless oil.
  • Step 4.4-Bromo-5-ethyl-5,6,7,8-tetrahydronaphthalen-2-ol To a 50-mL round- bottomed flask was added 2-(4-bromo-5-ethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-4,4,5,5- tetramethyl-1,3,2-dioxaborolane (0.20 g, 0.55 mmol) in tetrahydrofuran (1.6 mL) and water (0.6 mL).
  • the reaction was then stirred at this temperature for 2 h.
  • the reaction was then diluted with water (10 mL) and DCM (10 mL).
  • the mixture was transferred to a separatory funnel.
  • the layers were separated, and the aqueous layer was extracted with DCM (3 ⁇ 10 mL).
  • the organic layers were combined, dried with sodium sulfate, filtered, and concentrated under reduced pressure to provide a crude orange oil.
  • Step 2 (R)-1-(7-Chloro-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin- 7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)piperidine-3-sulfonamide.
  • Step 3 (R)-1-(7-(8-Ethyl-7-fluoro-3-(methoxymethoxy)naphthalen-1-yl)-8- fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidin-4-yl)piperidine-3-sulfonamide.
  • the vial was purged with nitrogen and the reactants were suspended in degassed tetrahydrofuran (0.9 mL) and water (90 ⁇ L). The reaction was then sealed and heated to 70 °C for 12 h. The reaction was concentrated under reduced pressure to provide a black oil.
  • Step 4 (R)-1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2- (((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidin-4-yl)piperidine-3-sulfonamide.
  • Table 3 SFC conditions for chiral separation.
  • Example 15 To a 20-mL vial was added 1-(7-(8-ethyl-7-fluoro-3-(methoxymethoxy)naphthalen- 1-yl)-8-fluoro-2-(((2S,7aR)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidin-4-yl)piperidin-3-ol (0.10 g, 0.16 mmol, synthesized in an analogous manner to Example 1) and sodium hydride (19 mg, 0.47 mmol, TCI America) in tetrahydrofuran (1.6 mL) at 0 °C.
  • Step 1 1-(7-Chloro-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin- 7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-5,5-dimethylpiperidine-3-carboxamide.
  • Step 2 1-(7-(8-Ethyl-7-fluoro-3-(methoxymethoxy)naphthalen-1-yl)-8-fluoro-2- (((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidin-4-yl)-5,5-dimethylpiperidine-3-carboxamide.
  • the vial was purged with nitrogen and the reactants were suspended in degassed tetrahydrofuran (0.9 mL) and water (0.09 mL). The reaction was then sealed and stirred at 65 °C overnight. The reaction was then cooled to rt and concentrated under reduced pressure to afford a crude black oil.
  • Step 3 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)- 2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-5,5- dimethylpiperidine-3-carboxamide.1-(7-(8-Ethyl-7-fluoro-3- (methoxymethoxy)naphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin- 7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-5,5-dimethylpiperidine-3-carboxamide (60 mg, 0.09 mmol
  • Step 2 N-((R)-1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2- (((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidin-4-yl)piperidin-3-yl)acetamide.
  • reaction mixture was purified by reverse phase HPLC to afford N-((R)-1-(7-(8- ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H- pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)piperidin-3-yl)acetamide bis(2,2,2-trifluoroacetate) (18 mg, 0.02 mmol, 38 % yield) as yellow solid.
  • Table 7 SFC Conditions for Chiral Separation.
  • Table 8 Analytical Data of Examples 44 to 78.
  • Step 2 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)- 2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-N- methylpiperidine-3-sulfonamide.1-(7-(8-Ethyl-7-fluoro-3-(methoxymethoxy)naphthalen-1- yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidin-4-yl)-N-methylpiperidine-3-sulfonamide (47 mg, 0.066
  • Example 132 To a 10-mL round-bottomed flask was added 4-(4-((R)-3-aminoazepan-1-yl)-8- fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidin-7-yl)-5-ethyl-6-fluoronaphthalen-2-ol (30 mg, 0.05 mmol) and DIPEA (32 mg, 43 ⁇ L, 0.25 mmol, Sigma-Aldrich Corporation) in DCM (0.5 mL).
  • Example 138 To an 8-mL vial was added methyl (R)-1-(7-(8-ethyl-7-fluoro-3- (methoxymethoxy)naphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin- 7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)piperidine-3-carboxylate (10 mg, 0.02 mmol) and 2 N sodium hydroxide (22 ⁇ L, 0.04 mmol, Sigma-Aldrich) and THF (74 ⁇ L). The reaction was stirred at rt overnight.
  • Example 141 To a 10-mL round-bottomed flask was added 1-(7-(8-ethyl-7-fluoro-3- (methoxymethoxy)naphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin- 7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)azepan-4-one (30 mg, 0.046 mmol) and sodium borohydride (5.2 mg, 0.14 mmol) in DCE (0.23 mL). A small amount of MeOH was added and the reaction was stirred at rt for 1 h.
  • Example 143 To a 10-mL round-bottomed flask was added 1-(7-(8-ethyl-7-fluoro-3- (methoxymethoxy)naphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin- 7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)azepan-4-one (20 mg, 0.03 mmol), ammonium acetate (24 mg, 0.31 mmol, Oakwood Products, Inc.) and methanol (0.6 mL).
  • Example 144 To a 25-mL round-bottomed flask was added methyltriphenylphosphonium bromide in THF (41 mg, 0.12 mmol, Sigma-Aldrich Corporation) and THF (0.4 mL). LiHMDS in (1.0 M in THF, 0.1 mL, 0.11 mmol, Sigma-Aldrich Corporation) was added. The reaction was stirred for 1 h.
  • Example 163 1-(7-(8-Ethyl-7-fluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2- fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)-5- methylpiperidine-3-carboxamide (Example 163 and Example 164) Synthesized in an analogous manner to Example 162, using 5-methylpiperidine-3- carboxamide hydrochloride (CAS#: 2228678-05-3, Enamine). Isomer 1 (Example 163) was isolated as bis(2,2,2-trifluoroacetate) and as light-yellow solid.
  • Step 1 4-Chloro-7-(7,8-difluoro-3-((triisopropylsilyl)oxy)naphthalen-1-yl)-8- fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidine.
  • Step 2 (R)-1-(7-(7,8-Difluoro-3-((triisopropylsilyl)oxy)naphthalen-1-yl)-8- fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3- d]pyrimidin-4-yl)piperidine-3-sulfonamide.
  • reaction mixture was purified by reverse phase HPLC to afford (R)-1-(7-(7,8-difluoro-3- ((triisopropylsilyl)oxy)naphthalen-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H- pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4-yl)piperidine-3-sulfonamide (5.0 mg, 6.23 ⁇ mol, 16 % yield) as white solid.
  • Step 3 (R)-1-(7-(7,8-Difluoro-3-hydroxynaphthalen-1-yl)-8-fluoro-2-(((2R,7aS)- 2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methoxy)pyrido[4,3-d]pyrimidin-4- yl)piperidine-3-sulfonamide.
  • Example 166 4-(4-(Azepan-1-yl)-8-fluoro-2-(((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)- yl)methoxy)pyrido[4,3-d]pyrimidin-7-yl)-5,6-difluoronaphthalen-2-ol (Example 166) Synthesized in an analogous manner to Example 165 using azepane (CAS#: 111-49- 9, Sigma-Aldrich Corporation). The product was isolated as its TFA salt. m/z (ESI, +ve ion): 582.0 (M+H) + .
  • Example 180 (R)-1-(2-((1-((Dimethylamino)methyl)cyclopropyl)methoxy)-7-(8-ethyl-7-fluoro-3- hydroxynaphthalen-1-yl)-8-fluoropyrido[4,3-d]pyrimidin-4-yl)-3-methylpiperidin-3-ol (Example 180).
  • Example 180 Synthesized in an analogous manner to Example 178 using (1- [(dimethylamino)methyl]cyclopropyl)methanol (CAS#: 39943-41-4, Enamine) and Lithium bis(trimethylsilyl)amide in THF solution (1 M). The product was isolated as off-white solid.
  • KRAS G12D TR-FRET Assay Compounds of interest were prepared in a dose-response titration in DMSO, and 80 nL were added via Labcyte Echo to each well of a 384-well plate (Perkin Elmer 6008280).
  • the His-tagged KRAS G12D protein (Amgen) was diluted to 20 nM in Assay Buffer (20 mM HEPES, pH 7.4, 10 mM MgCl 2 , 50 mM NaCl, 0.1% BSA, 0.01% Tween-20, 10 ⁇ M GDP) and 2 uL was added to the appropriate wells of the 384-well plate.
  • Biotinylated KRPep-2d substrate (Amgen) was diluted to 20 nM in Assay Buffer and 2 ⁇ L was added to all wells and incubated for 1 hour at room temperature.
  • Detection Reagent (0.4 nM LANCE Eu-W1024 Anti-6xHis (Perkin Elmer AD0401), 5 nM streptavidin-d2 (Cisbio 610SADLA) was prepared in Assay Buffer, then 4 ⁇ L was added to the plate and incubated for 1 hour at room temperature.
  • KRAS G12D Coupled Nucleotide Exchange Assay Purified GDP-bound KRAS protein (aa 1-169), containing both G12D and C118A amino acid substitutions and an N-terminal His-tag, was pre-incubated in assay buffer (25 mM HEPES pH 7.4, 10 mM MgCl 2 , and 0.01% Triton X-100) with a compound dose- response titration for 2 hours.
  • purified SOS protein (aa 564-1049) and GTP (Roche 10106399001) were added to the assay wells and incubated for an additional 30 min.
  • purified GST-tagged cRAF (aa 1-149), nickel chelate AlphaLISA acceptor beads (PerkinElmer AL108R), and AlphaScreen glutathione donor beads (PerkinElmer 6765302) were added to the assay wells and incubated for 10 minutes.
  • the assay plates were then read on a PerkinElmer EnVision Multilabel Reader, using AlphaScreen® technology, and data were analyzed using a 4-parameter logistic model to calculate IC 50 values.
  • AsPC-1 AsPC-1 (ATCC® CRL-1682TM) cells were cultured in RPMI 1640 Medium (ThermoFisher Scientific 11875093) containing 10% fetal bovine serum (ThermoFisher Scientific 16000044) and 1x penicillin-streptomycin-glutamine (ThermoFisher Scientific 10378016). Sixteen hours prior to compound treatment, AsPC-1 cells were seeded in 96-well cell culture plates at a density of 25,000 cells/well and incubated at 37 °C, 5% CO 2 .
  • a compound dose-response titration was diluted in growth media, added to appropriate wells of a cell culture plate, and then incubated at 37 °C, 5% CO 2 for 2 hours. Following compound treatment, cells were washed with ice-cold Dulbecco's phosphate-buffered saline, no Ca 2+ or Mg 2+ (ThermoFisher Scientific 14190144), and then lysed in RIPA buffer (50 mM Tris-HCl pH 7.5, 1% Igepal, 0.5% sodium deoxycholate, 150 mM NaCl, and 0.5% sodium dodecyl sulfate) containing protease inhibitors (Roche 4693132001) and phosphatase inhibitors (Roche 4906837001).
  • RIPA buffer 50 mM Tris-HCl pH 7.5, 1% Igepal, 0.5% sodium deoxycholate, 150 mM NaCl, and 0.5% sodium dodecyl sulfate
  • Phosphorylation of ERK1/2 in compound-treated lysates was assayed using Phospho-ERK1/2 Whole Cell Lysate kits (Meso Scale Discovery K151DWD) according to the manufacturer’s protocol. Assay plates were read on a Meso Scale Discovery Sector Imager 6000, and data were analyzed using a 4-parameter logistic model to calculate IC 50 values. Table 13: Biochemical and cellular activity of examples.

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Abstract

La présente invention concerne des composés utiles pour l'inhibition de KRAS G12D. Les composés ont une formule générale (I), les variables de la formule I étant définies dans la description. L'invention concerne également des compositions pharmaceutiques comprenant les composés, des utilisations des composés et des compositions pour traiter par exemple le cancer.
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