WO2023051681A1 - 四元稠环类化合物及其制备方法和应用 - Google Patents
四元稠环类化合物及其制备方法和应用 Download PDFInfo
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- WO2023051681A1 WO2023051681A1 PCT/CN2022/122536 CN2022122536W WO2023051681A1 WO 2023051681 A1 WO2023051681 A1 WO 2023051681A1 CN 2022122536 W CN2022122536 W CN 2022122536W WO 2023051681 A1 WO2023051681 A1 WO 2023051681A1
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- Prior art keywords
- compound
- alkyl
- pharmaceutically acceptable
- acceptable salt
- stereoisomer
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- 125000003660 2,3-dimethylpentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000003764 2,4-dimethylpentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical compound C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 description 1
- 125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000004336 3,3-dimethylpentyl group Chemical group [H]C([H])([H])C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- WSNKEJIFARPOSQ-UHFFFAOYSA-N 3-[4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-yl]oxy-N-(1-benzothiophen-2-ylmethyl)benzamide Chemical compound NCC1=CC(=NC(=C1)C(F)(F)F)OC=1C=C(C(=O)NCC2=CC3=C(S2)C=CC=C3)C=CC=1 WSNKEJIFARPOSQ-UHFFFAOYSA-N 0.000 description 1
- 125000004337 3-ethylpentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003469 3-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- 208000016557 Acute basophilic leukemia Diseases 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
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- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 208000031637 Erythroblastic Acute Leukemia Diseases 0.000 description 1
- 208000036566 Erythroleukaemia Diseases 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 108700020796 Oncogene Proteins 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 102000000395 SH3 domains Human genes 0.000 description 1
- 108050008861 SH3 domains Proteins 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- CSCPPACGZOOCGX-WFGJKAKNSA-N acetone d6 Chemical compound [2H]C([2H])([2H])C(=O)C([2H])([2H])[2H] CSCPPACGZOOCGX-WFGJKAKNSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 208000021841 acute erythroid leukemia Diseases 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 125000003725 azepanyl group Chemical group 0.000 description 1
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 1
- 210000003719 b-lymphocyte Anatomy 0.000 description 1
- 150000001602 bicycloalkyls Chemical group 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 238000005251 capillar electrophoresis Methods 0.000 description 1
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- 229910052801 chlorine Inorganic materials 0.000 description 1
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- CHVJITGCYZJHLR-UHFFFAOYSA-N cyclohepta-1,3,5-triene Chemical group C1C=CC=CC=C1 CHVJITGCYZJHLR-UHFFFAOYSA-N 0.000 description 1
- 125000003678 cyclohexadienyl group Chemical group C1(=CC=CCC1)* 0.000 description 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 150000001975 deuterium Chemical group 0.000 description 1
- 125000004852 dihydrofuranyl group Chemical group O1C(CC=C1)* 0.000 description 1
- 125000005047 dihydroimidazolyl group Chemical group N1(CNC=C1)* 0.000 description 1
- 125000005052 dihydropyrazolyl group Chemical group N1(NCC=C1)* 0.000 description 1
- 125000005054 dihydropyrrolyl group Chemical group [H]C1=C([H])C([H])([H])C([H])([H])N1* 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
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- 230000000857 drug effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 210000003958 hematopoietic stem cell Anatomy 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 125000002632 imidazolidinyl group Chemical group 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229960000310 isoleucine Drugs 0.000 description 1
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- FJUXWCBISHILFS-UHFFFAOYSA-N methyl 3,4-diamino-5-bromobenzoate Chemical compound COC(=O)C1=CC(N)=C(N)C(Br)=C1 FJUXWCBISHILFS-UHFFFAOYSA-N 0.000 description 1
- PRTLMEWWYBJZPN-UHFFFAOYSA-N methyl 4-amino-3-bromo-5-nitrobenzoate Chemical compound COC(=O)C1=CC(Br)=C(N)C([N+]([O-])=O)=C1 PRTLMEWWYBJZPN-UHFFFAOYSA-N 0.000 description 1
- 125000002911 monocyclic heterocycle group Chemical group 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- 230000007498 myristoylation Effects 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 210000005259 peripheral blood Anatomy 0.000 description 1
- 239000011886 peripheral blood Substances 0.000 description 1
- 210000004214 philadelphia chromosome Anatomy 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000026731 phosphorylation Effects 0.000 description 1
- 238000006366 phosphorylation reaction Methods 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 229940002612 prodrug Drugs 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000008844 regulatory mechanism Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000011301 standard therapy Methods 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 208000016595 therapy related acute myeloid leukemia and myelodysplastic syndrome Diseases 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 description 1
- 230000005945 translocation Effects 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/02—Seven-membered rings
- C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D267/16—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/22—Eight-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
Definitions
- the invention belongs to the field of medicine and biology, and specifically relates to four-membered condensed ring compounds and their preparation methods and applications, and also relates to the application of their pharmaceutically acceptable salts and pharmaceutical compositions in the treatment of cancer and other related diseases.
- CML chronic myelogenous leukemia
- Ph Philadelphia chromosome
- This chromosome carries the BCR-ABL1 oncogene, which encodes a chimeric BCR-ABL1 protein that lacks an N-terminal cap and has a constitutively active tyrosine kinase domain.
- Tyrosine kinase inhibitors (TKIs) targeting the BCR-ABL1 protein are standard therapy for CML patients, and imatinib, nilotinib, and dasatinib are approved for the treatment of newly diagnosed CML patients.
- BCR-ABL1 fusion protein is also the cause of acute lymphoblastic leukemia in a certain proportion, and drugs targeting ABL kinase activity can also be used for this indication, therefore, more BCR-ABL1 inhibition is needed clinically agent.
- the object of the present invention is to provide a compound shown in formula (I), its stereoisomer or its pharmaceutically acceptable salt:
- Ring A is selected from C 3-6 cycloalkyl, 4-7 membered heterocyclic group, C 6-10 aryl or 5-7 membered heteroaryl;
- R 1 is selected from hydrogen, deuterium, halogen, amino, hydroxyl, cyano, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 deuterated alkyl, C 1-6 6 haloalkyl, C 1-6 hydroxyalkyl, C 1-6 alkoxy, C 1-6 alkylthio or C 1-6 haloalkoxy;
- M 1 is selected from N or CR a ;
- M 2 is selected from NR a or C(R a ) 2 ;
- M 3 is selected from N or CR a ;
- R a is each independently selected from hydrogen, C 1-6 alkyl, C 1-6 deuterated alkyl, C 1-6 haloalkyl, C 1-6 hydroxyalkyl, C 1-6 alkoxy, C 1 -6 alkylthio or C 1-6 haloalkoxy;
- R 2 or R 3 are each independently selected from hydrogen, C 1-6 alkyl, C 1-6 deuterated alkyl, C 1-6 haloalkyl, C 1-6 hydroxyalkyl, C 1-6 alkoxy , C 1-6 alkylthio, C 1-6 haloalkoxy, C 3-6 cycloalkyl, 4-7 membered heterocyclyl, C 6-10 aryl or 5-7 membered heteroaryl;
- n 0, 1 or 2.
- Ring A is C 6-10 aryl or 5-6 membered heteroaryl
- R 1 is selected from C 1-3 alkyl, C 1-3 deuterated alkyl, C 1-3 haloalkyl, C 1-3 hydroxyalkyl, C 1-3 alkoxy, C 13 alkylthio or C 1-3 haloalkoxy;
- M1 is selected from N or CH;
- M 2 is selected from NH or CH 2 ;
- M is selected from N or CH
- R 2 or R 3 are each independently selected from C 1-3 alkyl, C 1-3 deuterated alkyl, C 1-3 haloalkyl, C 1-3 hydroxyalkyl, C 1-3 alkoxy, C 1-3 alkylthio or C 1-3 haloalkoxy.
- Ring A is phenyl or pyridyl
- R 1 is selected from C 1-3 alkyl, C 1-3 haloalkyl, C 1-3 alkoxy or C 1-3 haloalkoxy;
- M 1 is N
- M2 is NH
- R 2 or R 3 are each independently selected from hydrogen, C 1-3 alkyl or C 1-3 haloalkyl.
- R 1 is selected from -CF 2 , -CF 3 , -CF 2 Cl, -OCF 2 , -OCF 3 or -OCF 2 Cl;
- Each of R 2 or R 3 is independently selected from -CH 3 , -CF 2 , -CF 3 or -CF 2 Cl.
- the pharmaceutically acceptable salt is selected from sulfate, hydrochloride, ethylsulfonate, methanesulfonate, p-toluenesulfonate, benzenesulfonate, isethionate sulfonate or 1,5-naphthalene disulfonate, more preferably p-toluenesulfonate.
- the present invention provides a tosylate compound shown in formula (III):
- Ring A is selected from C 3-6 cycloalkyl, 4-7 membered heterocyclic group, C 6-10 aryl or 5-7 membered heteroaryl;
- R 1 is selected from hydrogen, deuterium, halogen, amino, hydroxyl, cyano, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 deuterated alkyl, C 1-6 6 haloalkyl, C 1-6 hydroxyalkyl, C 1-6 alkoxy, C 1-6 alkylthio or C 1-6 haloalkoxy;
- M 1 is selected from N or CR a ;
- M 2 is selected from NR a or C(R a ) 2 ;
- M 3 is selected from N or CR a ;
- R a is each independently selected from hydrogen, C 1-6 alkyl, C 1-6 deuterated alkyl, C 1-6 haloalkyl, C 1-6 hydroxyalkyl, C 1-6 alkoxy, C 1 -6 alkylthio or C 1-6 haloalkoxy;
- R 2 or R 3 are each independently selected from hydrogen, C 1-6 alkyl, C 1-6 deuterated alkyl, C 1-6 haloalkyl, C 1-6 hydroxyalkyl, C 1-6 alkoxy , C 1-6 alkylthio, C 1-6 haloalkoxy, C 3-6 cycloalkyl, 4-7 membered heterocyclyl, C 6-10 aryl or 5-7 membered heteroaryl;
- n 0, 1 or 2.
- Ring A is C 6-10 aryl or 5-6 membered heteroaryl
- R 1 is selected from C 1-3 alkyl, C 1-3 deuterated alkyl, C 1-3 haloalkyl, C 1-3 hydroxyalkyl, C 1-3 alkoxy, C 13 alkylthio or C 1-3 haloalkoxy;
- M1 is selected from N or CH;
- M 2 is selected from NH or CH 2 ;
- M is selected from N or CH
- R 2 or R 3 are each independently selected from C 1-3 alkyl, C 1-3 deuterated alkyl, C 1-3 haloalkyl, C 1-3 hydroxyalkyl, C 1-3 alkoxy, C 1-3 alkylthio or C 1-3 haloalkoxy.
- Ring A is phenyl or pyridyl
- R 1 is selected from C 1-3 alkyl, C 1-3 haloalkyl, C 1-3 alkoxy or C 1-3 haloalkoxy;
- M 1 is N
- M2 is NH
- R 2 or R 3 are each independently selected from hydrogen, C 1-3 alkyl or C 1-3 haloalkyl.
- R 1 is selected from -CF 2 , -CF 3 , -CF 2 Cl, -OCF 2 , -OCF 3 or -OCF 2 Cl;
- Each of R 2 or R 3 is independently selected from -CH 3 , -CH 2 CH 3 , -CF 2 , -CF 3 or -CF 2 Cl.
- the p-toluenesulfonate is selected from the following compounds:
- the object of the present invention is also to provide formula (II) compound, its stereoisomer or the method of pharmaceutically acceptable salt thereof,
- X is selected from halogen
- Ring A, R 1 -R 3 , M 1 -M 3 are defined as defined in general formula (II);
- the acid is preferably p-toluenesulfonic acid.
- the object of the present invention is also to provide formula (II) compound, its stereoisomer or the method of pharmaceutically acceptable salt thereof,
- X 1 , X 2 and X 3 are each independently selected from halogen;
- Ring A, R 1 -R 3 , M 1 -M 3 are defined as defined in general formula (II), preferably M 3 is N;
- the acid is preferably p-toluenesulfonic acid.
- the object of the present invention is also to provide a pharmaceutical composition, which contains a therapeutically effective amount of the compound of formula (I), its stereoisomer or its pharmaceutically acceptable salt, and one or more pharmaceutically acceptable carrier or excipient.
- the present invention also provides a compound of formula (I), its stereoisomer or a pharmaceutically acceptable salt thereof, and said pharmaceutical composition in the preparation of the inhibitor selected from Abelson protein (ABL1), Abelson-related protein (ABL2) and Application of chimeric protein BCR-ABL1 protein tyrosine kinase enzymatic activity in medicine.
- ABL1 Abelson protein
- ABL2 Abelson-related protein
- ABL1 Abelson-related protein
- chimeric protein BCR-ABL1 protein tyrosine kinase enzymatic activity in medicine.
- the present invention also provides the compound of formula (I), its stereoisomer or its pharmaceutically acceptable salt, and the application of its pharmaceutical composition in the preparation of medicines for leukemia-related diseases.
- the leukemia is chronic myelogenous leukemia (CML), acute myeloid leukemia (AML) or acute lymphoblastic leukemia (ALL).
- CML chronic myelogenous leukemia
- AML acute myeloid leukemia
- ALL acute lymphoblastic leukemia
- the CML is resistant to one or more of standard of care treatments such as imatinib, nilotinib and dasatinib, and the AML is secondary AML, which develops after myelodysplastic syndrome (MDS) or myeloproliferative neoplasm (MPN).
- MDS myelodysplastic syndrome
- MPN myeloproliferative neoplasm
- alkyl refers to a saturated aliphatic hydrocarbon group which is a straight or branched chain group containing 1 to 20 carbon atoms, preferably an alkyl group containing 1 to 8 carbon atoms, more preferably 1 to 6 carbon atoms An alkyl group, most preferably an alkyl group of 1 to 3 carbon atoms.
- Non-limiting examples include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, sec-butyl, n-pentyl, 1,1-dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1-ethylpropyl, 2-methylbutyl, 3-methylbutyl, n-hexyl, 1-ethyl-2- Methylpropyl, 1,1,2-trimethylpropyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 2,2-dimethylbutyl, 1,3 -Dimethylbutyl, 2-ethylbutyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 2,3-dimethylbutyl, n-heptyl, 2 -Methylhexyl, 3-methylhexyl, 4-methylhe
- lower alkyl groups containing 1 to 6 carbon atoms include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, sec-butyl Base, n-pentyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, 2-methylbutyl, 3-methylbutyl, n-hexyl, 1-ethyl-2-methylpropyl, 1,1,2-trimethylpropyl, 1,1-dimethylbutyl, 1,2-dimethyl Dimethylbutyl, 2,2-dimethylbutyl, 1,3-dimethylbutyl, 2-ethylbutyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl group, 2,3-dimethylbutyl group, etc.
- Alkyl groups may be substituted or unsubstituted, and when substituted, substituents may be substituted at any available point of attachment, said substituents being preferably one or more of the following groups independently selected from alkyl radical, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkane Oxygen, heterocycloalkoxy, cycloalkylthio, heterocycloalkylthio, oxo, carboxyl or carboxylate, preferably methyl, ethyl, isopropyl, tert-butyl, haloalkyl in the present invention , deuterated alkyl, alkoxy substituted alkyl and hydroxy substituted alkyl.
- cycloalkyl refers to a saturated or partially unsaturated monocyclic or polycyclic cyclic hydrocarbon substituent, the cycloalkyl ring containing 3 to 20 carbon atoms, preferably containing 3 to 12 carbon atoms, more preferably containing 3 to 8 carbon atoms, most preferably 3 to 6 carbon atoms.
- Non-limiting examples of monocyclic cycloalkyls include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cyclohexadienyl, cycloheptyl, cycloheptatriene group, cyclooctyl group, etc.; polycyclic cycloalkyl group includes spiro ring, fused ring and bridged ring cycloalkyl group, preferably cyclopropyl group, cyclobutyl group, cyclohexyl group, cyclopentyl group and cycloheptyl group.
- spirocycloalkyl refers to a polycyclic group of 5 to 20 membered monocyclic rings sharing one carbon atom (called a spiro atom), which may contain one or more double bonds, but none of the rings has complete conjugation The ⁇ -electron system. Preferably it is 6 to 14 yuan, more preferably 7 to 10 yuan. According to the number of spiro atoms shared between the rings, the spirocycloalkyl group can be divided into single spirocycloalkyl, double spirocycloalkyl or polyspirocycloalkyl, preferably single spirocycloalkyl and double spirocycloalkyl.
- spirocycloalkyl groups include:
- spirocycloalkyls in which a single spirocycloalkyl shares a spiro atom with a heterocycloalkyl, non-limiting examples include:
- fused cycloalkyl refers to a 5 to 20 membered all-carbon polycyclic group in which each ring of the system shares an adjacent pair of carbon atoms with other rings in the system, wherein one or more rings may contain one or Multiple double bonds, but none of the rings have a fully conjugated ⁇ -electron system.
- it is 6 to 14 yuan, more preferably 7 to 10 yuan.
- it can be divided into bicyclic, tricyclic, tetracyclic or polycyclic condensed cycloalkyl groups, preferably bicyclic or tricyclic, more preferably 5-membered/5-membered or 5-membered/6-membered bicycloalkyl groups.
- fused cycloalkyl groups include:
- bridged cycloalkyl refers to a 5 to 20 membered, all-carbon polycyclic group having any two rings sharing two carbon atoms not directly attached, which may contain one or more double bonds, but none of the rings has a complete Conjugated ⁇ -electron systems. Preferably it is 6 to 14 yuan, more preferably 7 to 10 yuan. According to the number of constituent rings, it can be divided into bicyclic, tricyclic, tetracyclic or polycyclic bridged cycloalkyl groups, preferably bicyclic, tricyclic or tetracyclic, more preferably bicyclic or tricyclic.
- bridged cycloalkyl groups include:
- heterocyclyl refers to a saturated or partially unsaturated monocyclic or polycyclic cyclic hydrocarbon substituent comprising 3 to 20 ring atoms, one or more of which is selected from nitrogen, oxygen, C(O) or a heteroatom of S(O) m (where m is an integer from 0 to 2), excluding ring portions of -OO-, -OS- or -SS-, the remaining ring atoms being carbon.
- the membered heterocyclic group is optionally substituted by 1-2 oxygen atoms, sulfur atoms, or oxo groups, including nitrogen-containing monocyclic heterocyclic groups, nitrogen-containing spiroheterocyclic groups or nitrogen-containing condensed heterocyclic groups.
- Non-limiting examples of monocyclic heterocyclyl groups include oxetanyl, azetidinyl, thietanyl, pyrrolidinyl, imidazolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, tetrahydropyranyl Base, dihydroimidazolyl, dihydrofuranyl, dihydropyrazolyl, dihydropyrrolyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, homopiperazinyl, azeptyl, 1,4-diazepanyl, pyranyl or tetrahydrothiopyranyl dioxide, etc.; preferably oxetanyl, azetidinyl, thietanyl, tetrahydrofuranyl, tetrahydro Pyranyl, tetrahydrothiophenyl, tetra
- Polycyclic heterocyclic groups include spiro rings, fused rings and bridged ring heterocyclic groups; the spiro rings, condensed rings and bridged ring heterocyclic groups involved are optionally connected to other groups through single bonds, or through rings Any two or more atoms on the ring are further linked with other cycloalkyl, heterocyclyl, aryl and heteroaryl groups.
- spiroheterocyclyl refers to a polycyclic heterocyclic group that shares one atom (called a spiro atom) between 5 to 20-membered monocyclic rings, wherein one or more ring atoms are selected from nitrogen, oxygen or S(O ) m (wherein m is an integer from 0 to 2), the remaining ring atoms are carbon. It may contain one or more double bonds, but none of the rings has a fully conjugated pi-electron system. Preferably it is 5 to 12 yuan, more preferably 7 to 10 yuan.
- the spiroheterocyclyl can be divided into single spiroheterocyclyl, double spiroheterocyclyl or polyspiroheterocyclyl, preferably single spiroheterocyclyl and double spiroheterocyclyl. More preferably, it is a 3-membered/5-membered, 3-membered/6-membered, 4-membered/4-membered, 4-membered/5-membered, 4-membered/6-membered, 5-membered/5-membered or 5-membered/6-membered monospiroheterocyclic group.
- spiroheterocyclyls include:
- fused heterocyclyl refers to a 5 to 20 membered polycyclic heterocyclic group in which each ring in the system shares an adjacent pair of atoms with other rings in the system, and one or more rings may contain one or more double bond, but none of the rings has a fully conjugated ⁇ -electron system, where one or more ring atoms are heteroatoms selected from nitrogen, oxygen, or S(O) m (where m is an integer from 0 to 2), and the remaining ring
- the atom is carbon.
- it is 6 to 14 yuan, more preferably 7 to 10 yuan.
- bicyclic, tricyclic, tetracyclic or polycyclic fused heterocyclic groups preferably bicyclic or tricyclic, more preferably 5-membered/5-membered or 5-membered/6-membered bicyclic fused heterocyclic groups.
- fused heterocyclic groups include:
- bridged heterocyclyl refers to a 5 to 14 membered polycyclic heterocyclic group in which any two rings share two atoms not directly attached, which may contain one or more double bonds, but none of the rings has a complete shared bond.
- it is 6 to 14 yuan, more preferably 6 to 10 yuan.
- bridged heterocyclyl groups include:
- the heterocyclyl ring may be fused to an aryl, heteroaryl, or cycloalkyl ring where the ring bonded to the parent structure is a heterocyclyl, non-limiting examples of which include:
- Heterocyclic groups may be optionally substituted or unsubstituted, and when substituted, the substituents are preferably one or more of the following groups independently selected from alkyl, alkenyl, alkynyl, alkoxy, alk Thio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio , heterocycloalkylthio, oxo, carboxyl or carboxylate.
- aryl refers to a 6 to 14 membered all-carbon monocyclic or fused polycyclic (that is, rings sharing adjacent pairs of carbon atoms) group, preferably 6 to 10 membered, having a conjugated pi-electron system, such as benzene base and naphthyl. Phenyl is more preferred.
- the aryl ring can be fused to a heteroaryl, heterocyclyl or cycloalkyl ring, including benzo 3-8 membered cycloalkyl, benzo 3-8 membered heteroalkyl, preferably benzo 3-6 Membered cycloalkyl, benzo 3-6 membered heteroalkyl, wherein the heterocyclic group is a heterocyclic group containing 1-3 nitrogen atoms, oxygen atoms, sulfur atoms; or a three-membered nitrogen-containing condensed ring containing a benzene ring , where the ring attached to the parent structure is an aryl ring.
- Aryl groups may be substituted or unsubstituted, and when substituted, the substituents are preferably one or more of the following groups independently selected from alkyl, alkenyl, alkynyl, alkoxy, alkylthio, Alkylamino, halogen, mercapto, hydroxy, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, heterocycle Alkylthio, carboxyl or carboxylate.
- heteroaryl refers to a heteroaromatic system comprising 1 to 4 heteroatoms, 5 to 14 ring atoms, wherein the heteroatoms are selected from oxygen, sulfur and nitrogen.
- Heteroaryl is preferably 5 to 10 membered, more preferably 5 or 6 membered, such as imidazolyl, furyl, thienyl, thiazolyl, pyrazolyl, oxazolyl, pyrrolyl, triazolyl, tetrazolyl , pyridyl, pyrimidyl, thiadiazole, pyrazinyl, etc., preferably triazolyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, pyrimidinyl or thiazolyl; more preferably pyrazolyl and oxa Azolyl.
- the heteroaryl ring may be fused to an aryl, heterocyclyl or cycloalkyl ring
- alkoxy refers to -O-(alkyl) and -O-(unsubstituted cycloalkyl), wherein alkyl is as defined above.
- alkoxy include: methoxy, ethoxy, propoxy, butoxy, cyclopropoxy, cyclobutoxy, cyclopentyloxy, cyclohexyloxy.
- Alkoxy may be optionally substituted or unsubstituted, and when substituted, the substituent is preferably one or more of the following groups independently selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkoxy Thio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio , heterocycloalkylthio, carboxyl or carboxylate.
- the substituent is preferably one or more of the following groups independently selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkoxy Thio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
- haloalkyl refers to an alkyl group substituted with one or more halo, wherein alkyl is as defined above.
- haloalkoxy refers to an alkoxy group substituted with one or more halogens, wherein alkoxy group is as defined above.
- hydroxyalkyl refers to an alkyl group substituted by a hydroxy group, wherein alkyl is as defined above.
- alkylthio refers to -S-(alkyl) and -S-(unsubstituted cycloalkyl), wherein alkyl is as defined above.
- alkylthio include: methylthio, ethylthio, propylthio, butylthio, cyclopropylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio, alkylthio can be is optionally substituted or unsubstituted, and when substituted, the substituent is preferably one or more of the following groups independently selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkane Amino, halogen, mercapto, hydroxyl, nitro, cyano, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloal
- Alkenyl refers to an alkenyl group, also known as an alkenyl group, which is a straight-chain or branched group containing 2 to 20 carbon atoms, preferably an alkenyl group containing 2 to 8 carbon atoms, more preferably 2 to 6 An alkenyl group of carbon atoms, most preferably an alkenyl group of 2 to 4 carbon atoms.
- alkenyl mentioned therein can be further substituted by other related groups, for example: alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, Cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, heterocycloalkylthio, carboxyl or carboxylate.
- other related groups for example: alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, Cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, heterocycloalkylthio, carboxyl or carboxylate.
- Alkynyl means a straight or branched chain group containing 2 to 20 carbon atoms, preferably an alkynyl group containing 2 to 8 carbon atoms, more preferably an alkynyl group containing 2 to 6 carbon atoms, and most preferably Alkynyl groups of 2 to 4 carbon atoms are preferred.
- alkynyl mentioned therein can be further substituted by other related groups, for example: alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, Cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, heterocycloalkylthio, carboxyl or carboxylate.
- other related groups for example: alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylamino, halogen, mercapto, hydroxyl, nitro, cyano, Cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkoxy, heterocycloalkoxy, cycloalkylthio, heterocycloalkylthio, carboxyl or carboxylate.
- Haldroxy means an -OH group.
- Halogen means fluorine, chlorine, bromine or iodine.
- Amino refers to -NH2 .
- Cyano refers to -CN.
- X is selected from A, B, or C
- X is selected from A, B, and C
- X is A, B, or C
- X is A, B, and C
- the hydrogen atoms described in the present invention can be replaced by its isotope deuterium, and any hydrogen atom in the example compounds involved in the present invention can also be replaced by a deuterium atom.
- Optional or “optionally” means that the subsequently described event or circumstance can but need not occur, and that the description includes instances where the event or circumstance occurs or does not occur.
- a heterocyclic group optionally substituted with an alkyl group means that an alkyl group may but need not be present, and the description includes cases where the heterocycle group is substituted with an alkyl group and cases where the heterocycle group is not substituted with an alkyl group .
- Substituted means that one or more hydrogen atoms in a group, preferably up to 5, more preferably 1 to 3 hydrogen atoms are independently substituted by the corresponding number of substituents. It goes without saying that substituents are only in their possible chemical positions and that a person skilled in the art can determine (by experiment or theory) possible or impossible substitutions without undue effort. For example, an amino or hydroxyl group with free hydrogen may be unstable when bonded to a carbon atom with an unsaturated (eg, ethylenic) bond.
- Optional substituents include deuterium, halogen, amino, hydroxyl, cyano, oxo, thio, alkyl, alkenyl, alkynyl, deuterated alkyl, haloalkyl, hydroxyalkyl, alkoxy , alkylthio, haloalkoxy, cycloalkyl, heterocyclyl, aryl and heteroaryl are substituted by one or more substituents, preferably deuterium, halogen, amino, hydroxyl, cyano, oxo, Thio group, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 deuterated alkyl, C 1-6 haloalkyl, C 1-6 hydroxyalkyl, C 1-6 alkoxy, C 1-6 alkylthio, C 1-6 haloalkoxy, C 3-12 cycloalkyl, 3-12 membered heterocyclyl, C 6-14 aryl and 5-14 member
- “Pharmaceutical composition” means a mixture containing one or more compounds described herein, or a physiologically/pharmaceutically acceptable salt or prodrug thereof, and other chemical components, and other components such as a physiologically/pharmaceutically acceptable carrier and excipients.
- the purpose of the pharmaceutical composition is to promote the administration to the organism, facilitate the absorption of the active ingredient and thus exert biological activity.
- “Pharmaceutically acceptable salt” refers to the salt of the compound of the present invention, which is safe and effective when used in mammals, and has proper biological activity.
- Step 1 Synthesis of 7-bromo-2-(difluoromethyl)-1H-difluoromethyl-benzo[d]imidazole-5-carboxylic acid methyl ester
- Step 2 (R)-7-bromo-2-(difluoromethyl)-1-[1-hydroxypropyl-2-yl]-1H-benzo[d]imidazole-5-carboxylic acid methyl ester synthesis
- Step 4 (3R)-2-(difluoromethyl)-3-methyl-3,4,5a,6-tetrahydro-5-oxa-1,2a,6,8-tetraazabenzo Synthesis of [4,5]cyclooctyl[1,2,3-cd]indene-11-carboxylic acid methyl ester
- Step 5 (3R)-N-(4-(chlorodifluoromethoxy)phenyl)-2-(difluoromethyl)-3-methyl-3,4,5a,6-tetrahydro-5 Synthesis of -oxa-1,2a,6,8-tetraazabenzo[4,5]cyclooctyl[1,2,3-cd]indene-11-carboxamide
- Step 6 (3R)-N-(4-(chlorodifluoromethoxy)phenyl)-2-(difluoromethyl)-3-methyl-3,4,5a,6-tetrahydro-5 Synthesis of -oxa-1,2a,6,8-tetraazabenzo[4,5]cyclooct[1,2,3-cd]indene-11-carboxamide 4-methylbenzenesulfonate
- reaction solution was concentrated to dryness, ethyl acetate and water were added to the residue for extraction, the organic phase was washed with saturated sodium chloride, and dried over anhydrous sodium sulfate. After filtration, the filtrate was purified by column chromatography to obtain 13.32 g of compound 3 with a yield of 55%.
- the capillary electrophoresis method is used to detect the phosphorylation conversion rate of the substrate peptide to determine the IC 50 value of the test compound for the inhibition of the kinase (ABL1-WT).
- the highest concentration of the compound detected in the test is 1000nM, 3-fold dilution, a total of 12 concentrations (1000-0.0056nM).
- the enzyme reaction system was prepared (the concentration of the enzyme ABL1-WT was 1.3 nM, the concentration of the substrate FLPeptide2 was 1.5 ⁇ M, and the reaction factor was 10 mM MgCl 2 ). After incubation at room temperature for 30 min, 5 ⁇ L of 4 ⁇ ATP solution was added to start the enzyme reaction.
- a stop buffer (containing 0.5M EDTA) was added to terminate the reaction.
- the samples were analyzed using EZ reader (analysis conditions: pressure-1.5PSI, upper voltage current-2250V, lower voltage current-500V, separation time 40sec, system delay 100.0sec).
- the conversion rate read by EZ Reader is used to calculate the remaining activity rate according to the following formula.
- XLfit was used to calculate IC 50 , and the fitting formula was selected from formula 201 to calculate IC 50 .
- Luminescent Cell Viability Assay Kit (Luminescent Cell Viability Assay) was used to detect the inhibitory effect of drugs on the proliferation and growth of tumor cells.
- the cells in the logarithmic growth phase of the overnight culture were directly collected and counted by pipetting, mixing, and the cell density was adjusted according to the different density requirements of the cells, and the cell suspension was prepared and spread on a 96-well plate.
- the highest detection concentration in Ba/F3 BCR-ABL1-T315I, Ba/F3 BCR-ABL1-E255K cells is 10000nM, 3.16 times serial dilution , a total of 9 concentrations (10000-1.0058nM), the highest concentration of the compound detected in other cells is 500nM, 3.16-fold serial dilution, a total of 9 concentrations (500-0.0503nM).
- the cells added with the compound were cultured for another 72 hours at 37° C., 5% CO 2 .
- the compound of the present invention can significantly inhibit the proliferation of Ba/F3 BCR-ABL1-T315I, E255K, E255V, G250E mutant cells.
- Luminescent Cell Viability Assay Kit ( Luminescent Cell Viability Assay) was used to detect the inhibitory effect of drugs on the proliferation and growth of tumor cells.
- the cells in the logarithmic growth phase of the overnight culture were directly collected and counted by pipetting, mixing, and the cell density was adjusted according to the different density requirements of the cells, and the cell suspension was prepared and spread on a 96-well plate.
- the cells added with the compound were cultured for another 72 hours at 37° C., 5% CO 2 .
- test results show that the compound of the present invention can significantly inhibit the proliferation of tumor cells with BCR-ABL1 fusion mutation.
- mice BALB/c nude mice, 8-10 weeks.
- a Take out a strain of KCL22-s cells from the cell bank, use RPMI-1640 medium (RPMI-1640+10%FBS+1%P/S) to resuscitate the cells, and place the resuscitated cells in the cell culture flask (in the bottle The cell type, date, cultivator’s name, etc. are marked on the wall) and placed in a CO 2 incubator for culture (the temperature of the incubator is 37° C., and the concentration of CO 2 is 5%).
- RPMI-1640 medium RPMI-1640+10%FBS+1%P/S
- the cells are subcultured, and the cells are continuously cultured in a CO 2 incubator after passage. This process is repeated until the number of cells meets the in vivo drug efficacy requirements.
- c. Collect the cultured cells, count them with an automatic cell counter, and resuspend the cells with PBS according to the counting results to make a cell suspension (density 5 ⁇ 10 7 /mL), and put them in an ice box until use.
- mice Inoculate nude mice in turn (each mouse is inoculated with 0.1 mL of cell suspension).
- the tumor was measured on the 15th day after inoculation, and the tumor size was calculated.
- tumor volume (mm 3 ) length (mm) x width (mm) x width (mm)/2
- test drug administration method: oral administration; administration dose: 1.5, 3, 7.5mg/kg; administration volume: 10mL/kg; administration frequency: 1-2 times/day ; Administration cycle: 15 days; Vehicle: 0.5% HPMC K4M).
- Tumors were measured and weighed twice a week after starting to administer the test drug.
- TGI (%) [1-(average tumor volume at the end of administration of a treatment group-average tumor volume at the beginning of administration of this treatment group)/average tumor volume at the beginning of administration of this treatment group] ⁇ 100%.
- the compound of the present invention has significant tumor-inhibiting effect on human chronic myeloid leukemia cell line KCL22-s xenograft tumor model.
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Abstract
Description
化合物 | 最高浓度(μM) | ABL1-WT IC 50(nM) |
实施例1 | 1 | 0.43 |
Claims (11)
- 式(I)所示化合物,其立体异构体或其药学上可接受的盐:其中:环A选自C 3-6环烷基、4-7元杂环基、C 6-10芳基或5-7元杂芳基;R 1选自氢、氘、卤素、氨基、羟基、氰基、C 1-6烷基、C 2-6烯基、C 2-6炔基、C 1-6氘代烷基、C 1-6卤代烷基、C 1-6羟烷基、C 1-6烷氧基、C 1-6烷硫基或C 1-6卤代烷氧基;M 1选自N或CR a;M 2选自NR a或C(R a) 2;M 3选自N或CR a;R a各自独立地选自氢、C 1-6烷基、C 1-6氘代烷基、C 1-6卤代烷基、C 1-6羟烷基、C 1-6烷氧基、C 1-6烷硫基或C 1-6卤代烷氧基;R 2或R 3各自独立地选自氢、C 1-6烷基、C 1-6氘代烷基、C 1-6卤代烷基、C 1-6羟烷基、C 1-6烷氧基、C 1-6烷硫基、C 1-6卤代烷氧基、C 3-6环烷基、4-7元杂环基、C 6-10芳基或5-7元杂芳基;n为0、1或2。
- 根据权利要求1所述的化合物,其立体异构体或其药学上可接受的盐,其特征在于,环A为C 6-10芳基或5-6元杂芳基;R 1选自C 1-3烷基、C 1-3氘代烷基、C 1-3卤代烷基、C 1-3羟烷基、C 1-3烷氧基、C 13烷硫基或C 1-3卤代烷氧基;M 1选自N或CH;M 2选自NH或CH 2;M 3选自N或CH;R 2或R 3各自独立地选自C 1-3烷基、C 1-3氘代烷基、C 1-3卤代烷基、C 1-3羟烷基、C 1-3烷氧基、C 1-3烷硫基或C 1-3卤代烷氧基。
- 根据权利要求3所述的化合物,其立体异构体或其药学上可接受的盐,其特征在于,环A为苯基或吡啶基;R 1选自C 1-3烷基、C 1-3卤代烷基、C 1-3烷氧基或C 1-3卤代烷氧基;M 1为N;M 2为NH;M 3为N;R 2或R 3各自独立地选自氢、C 1-3烷基或C 1-3卤代烷基。
- 根据权利要求1-4任一项权利要求所述的化合物,其立体异构体或其药学上可接受的盐,其特征在于,R 1选自-CF 2、-CF 3、-CF 2Cl、-OCF 2、-OCF 3或-OCF 2Cl;R 2或R 3各自独立地选自-CH 3、-CH 2CH 3、-CF 2、-CF 3或-CF 2Cl。
- 根据权利要求1-6所述的化合物,其立体异构体或其药学上可接受的盐,其特征在于,药学上可接受的盐选自硫酸盐、盐酸盐、乙基磺酸盐、甲磺酸盐、对甲苯磺酸盐、苯磺酸盐、羟乙基磺酸盐或1,5-萘二磺酸盐,优选对甲苯磺酸盐。
- 一种药物组合物,其含有治疗有效量的权利要求1-7任一项所述化合物,其立体异构体或其药学上可接受的盐,以及一种或多种药学上可接受的载体或赋形剂。
- 根据权利要求1-7任一项所述化合物,其立体异构体或其药学上可接受的盐,以及权利要求8所述的药物组合物在制备ABL1和/或BCR-ABL1酪氨酸激酶抑制剂中的应用。
- 根据权利要求1-7任一项所述化合物,其立体异构体或其药学上可接受的盐,以及权利要求8所述的药物组合物在制备治疗白血病相关疾病药物中的应用,优选地,所述白血病选自慢性骨髓性白血病,急性髓性白血病或急性淋巴细胞性白血病。
- 一种制备式(II)化合物,其立体异构体或其药学上可接受的盐的方法,化合物1与化合物2发生取代反应制备化合物3,在硼酸化合物4作用下制备化合物5,化合物5在酸性条件下制备成环化合物6,与化合物7发生缩合反应制备得到(II)化合物,其立体异构体或其药学上可接受的盐;X选自卤素;环A、R 1-R 3、M 1-M 3的定义如权利要求3所述;或者,化合物1-a与化合物2发生取代反应制备化合物3-a,与3-b反应制备得到化合物5-a,化合物5-a在硼酸化合物4作用下制备化合物6-a,化合物6-a与化合物7发生缩合反应制备得到(II)化合物;任选地,到(II)化合物与酸反应制备得到盐化合物;X 1、X 2和X 3各自独立地选自卤素;环A、R 1-R 3、M 1-M 3的定义如通式(II)所定义,优选M 3为N;所述酸优选为对甲苯磺酸。
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US20040029850A1 (en) * | 2000-09-28 | 2004-02-12 | Peter Bernstein | Cyclized benzamide neurokinin antagonists for use in therapy |
CN103113355A (zh) * | 2013-02-27 | 2013-05-22 | 无锡爱内特生物科技有限公司 | 一种Bcr/Abl酪氨酸激酶抑制剂及其制备方法和在治疗慢性粒细胞白血病中的应用 |
CN109790144A (zh) * | 2016-04-29 | 2019-05-21 | 爱仕达生物技术有限责任公司 | 新型杂环化合物作为酪氨酸激酶bcr-abl抑制剂 |
US20210101872A1 (en) * | 2018-03-09 | 2021-04-08 | The Usa, As Represented By The Secretary, Dept. Of Health And Human Services | C-abl tyrosine kinase inhibitory compound embodiments and methods of making and using the same |
-
2022
- 2022-09-29 WO PCT/CN2022/122536 patent/WO2023051681A1/zh active Application Filing
- 2022-09-29 AU AU2022355393A patent/AU2022355393A1/en active Pending
- 2022-09-29 CA CA3234312A patent/CA3234312A1/en active Pending
- 2022-09-30 TW TW111137341A patent/TW202330547A/zh unknown
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US20040029850A1 (en) * | 2000-09-28 | 2004-02-12 | Peter Bernstein | Cyclized benzamide neurokinin antagonists for use in therapy |
CN103113355A (zh) * | 2013-02-27 | 2013-05-22 | 无锡爱内特生物科技有限公司 | 一种Bcr/Abl酪氨酸激酶抑制剂及其制备方法和在治疗慢性粒细胞白血病中的应用 |
CN109790144A (zh) * | 2016-04-29 | 2019-05-21 | 爱仕达生物技术有限责任公司 | 新型杂环化合物作为酪氨酸激酶bcr-abl抑制剂 |
US20210101872A1 (en) * | 2018-03-09 | 2021-04-08 | The Usa, As Represented By The Secretary, Dept. Of Health And Human Services | C-abl tyrosine kinase inhibitory compound embodiments and methods of making and using the same |
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CA3234312A1 (en) | 2023-04-06 |
AU2022355393A1 (en) | 2024-05-09 |
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