TWI831855B - 新穎吲唑化合物或其鹽 - Google Patents

Info

Publication number

TWI831855B

TWI831855B TW108138686A TW108138686A TWI831855B TW I831855 B TWI831855 B TW I831855B TW 108138686 A TW108138686 A TW 108138686A TW 108138686 A TW108138686 A TW 108138686A TW I831855 B TWI831855 B TW I831855B

Authority

TW

Taiwan

Prior art keywords

group

methyl

substituent

chloro

tert

Prior art date

2018-10-26

Links

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• -1 indazole compound Chemical class 0.000 claims abstract description 305
• 150000003839 salts Chemical class 0.000 claims abstract description 115
• 125000001424 substituent group Chemical group 0.000 claims description 410
• 150000001875 compounds Chemical class 0.000 claims description 227
• 125000000623 heterocyclic group Chemical group 0.000 claims description 141
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 133
• 238000004519 manufacturing process Methods 0.000 claims description 113
• 125000005843 halogen group Chemical group 0.000 claims description 110
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 101
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 94
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 91
• 229910052757 nitrogen Inorganic materials 0.000 claims description 81
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 72
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 68
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 65
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 57
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 55
• 229910052799 carbon Inorganic materials 0.000 claims description 46
• 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 43
• 125000004434 sulfur atom Chemical group 0.000 claims description 41
• 125000003277 amino group Chemical group 0.000 claims description 40
• 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 39
• 229910052801 chlorine Inorganic materials 0.000 claims description 38
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 38
• 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 37
• 125000000217 alkyl group Chemical group 0.000 claims description 35
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 34
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 33
• 206010028980 Neoplasm Diseases 0.000 claims description 29
• 239000002246 antineoplastic agent Substances 0.000 claims description 28
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 28
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 27
• 229920002554 vinyl polymer Polymers 0.000 claims description 25
• 125000005842 heteroatom Chemical group 0.000 claims description 24
• 125000000392 cycloalkenyl group Chemical group 0.000 claims description 21
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 21
• 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 20
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 19
• NFTAFPLJYLZTAU-UHFFFAOYSA-N 5-tert-butyl-6-chloro-1H-indazol-3-amine Chemical compound C(C)(C)(C)C=1C=C2C(=NNC2=CC1Cl)N NFTAFPLJYLZTAU-UHFFFAOYSA-N 0.000 claims description 19
• 229910052805 deuterium Inorganic materials 0.000 claims description 18
• 229910052717 sulfur Inorganic materials 0.000 claims description 18
• 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 16
• 125000004432 carbon atom Chemical group C* 0.000 claims description 15
• 125000003342 alkenyl group Chemical group 0.000 claims description 14
• 239000004480 active ingredient Substances 0.000 claims description 13
• 125000000530 1-propynyl group Chemical group [H]C([H])([H])C#C* 0.000 claims description 10
• 125000001188 haloalkyl group Chemical group 0.000 claims description 10
• 125000003545 alkoxy group Chemical group 0.000 claims description 9
• 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 8
• 239000003814 drug Substances 0.000 claims description 8
• 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 7
• 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims description 7
• ZHNUHDYFZUAESO-UHFFFAOYSA-N formamide Substances NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims description 7
• 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 6
• 125000006222 dimethylaminomethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])* 0.000 claims description 6
• 239000008194 pharmaceutical composition Substances 0.000 claims description 5
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
• 125000003118 aryl group Chemical group 0.000 claims description 4
• 239000003937 drug carrier Substances 0.000 claims description 4
• ZBNZAJFNDPPMDT-UHFFFAOYSA-N 1h-imidazole-5-carboxamide Chemical compound NC(=O)C1=CNC=N1 ZBNZAJFNDPPMDT-UHFFFAOYSA-N 0.000 claims 1
• XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical group N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims 1
• 125000004431 deuterium atom Chemical group 0.000 claims 1
• 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 604
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 294
• 239000000243 solution Substances 0.000 description 223
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 175
• 239000000203 mixture Substances 0.000 description 131
• 239000002904 solvent Substances 0.000 description 119
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 116
• 238000006243 chemical reaction Methods 0.000 description 108
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 108
• 239000012044 organic layer Substances 0.000 description 104
• 230000002829 reductive effect Effects 0.000 description 101
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 99
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 98
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 92
• 238000004440 column chromatography Methods 0.000 description 92
• PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 89
• 229910052938 sodium sulfate Inorganic materials 0.000 description 89
• 235000011152 sodium sulphate Nutrition 0.000 description 89
• 235000002639 sodium chloride Nutrition 0.000 description 85
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 78
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 75
• HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 72
• 238000003756 stirring Methods 0.000 description 60
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 53
• 238000000746 purification Methods 0.000 description 53
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 51
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 46
• 238000000034 method Methods 0.000 description 45
• 239000000126 substance Substances 0.000 description 43
• UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 42
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 42
• 239000007864 aqueous solution Substances 0.000 description 42
• 238000001816 cooling Methods 0.000 description 38
• DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 35
• 239000002585 base Substances 0.000 description 35
• 150000001721 carbon Chemical group 0.000 description 35
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 33
• RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 33
• 125000001153 fluoro group Chemical group F* 0.000 description 29
• JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 28
• KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 28
• 229910052731 fluorine Inorganic materials 0.000 description 26
• KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 24
• 239000011541 reaction mixture Substances 0.000 description 24
• 102100030708 GTPase KRas Human genes 0.000 description 23
• 101000584612 Homo sapiens GTPase KRas Proteins 0.000 description 23
• 125000000753 cycloalkyl group Chemical group 0.000 description 23
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 22
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 22
• NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 20
• MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 20
• PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 20
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 20
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 20
• SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 19
• 239000012295 chemical reaction liquid Substances 0.000 description 19
• 239000010410 layer Substances 0.000 description 19
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 18
• 239000003795 chemical substances by application Substances 0.000 description 18
• 239000007787 solid Substances 0.000 description 18
• 150000001975 deuterium Chemical group 0.000 description 17
• 229920006395 saturated elastomer Polymers 0.000 description 17
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 16
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 16
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 16
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 16
• RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 16
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
• 239000002253 acid Substances 0.000 description 15
• 125000002950 monocyclic group Chemical group 0.000 description 15
• 230000035772 mutation Effects 0.000 description 15
• 125000006239 protecting group Chemical group 0.000 description 15
• 235000017557 sodium bicarbonate Nutrition 0.000 description 15
• 229910000030 sodium bicarbonate Inorganic materials 0.000 description 15
• OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 14
• JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 14
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 14
• 102200006538 rs121913530 Human genes 0.000 description 14
• 150000002430 hydrocarbons Chemical group 0.000 description 13
• 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 12
• WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 12
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 12
• 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 12
• LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 12
• 125000006017 1-propenyl group Chemical group 0.000 description 11
• 201000011510 cancer Diseases 0.000 description 11
• 150000002148 esters Chemical class 0.000 description 11
• 239000000706 filtrate Substances 0.000 description 11
• RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 10
• VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 10
• WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 10
• 239000003153 chemical reaction reagent Substances 0.000 description 10
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 10
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 10
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 10
• 125000003386 piperidinyl group Chemical group 0.000 description 10
• 229910000027 potassium carbonate Inorganic materials 0.000 description 10
• 229910000029 sodium carbonate Inorganic materials 0.000 description 10
• 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 9
• BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical group OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 9
• WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 9
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
• 125000003282 alkyl amino group Chemical group 0.000 description 9
• 229910000147 aluminium phosphate Inorganic materials 0.000 description 9
• 235000019270 ammonium chloride Nutrition 0.000 description 9
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 9
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 9
• 229910052763 palladium Inorganic materials 0.000 description 9
• 125000000719 pyrrolidinyl group Chemical group 0.000 description 9
• 239000000725 suspension Substances 0.000 description 9
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
• CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 8
• LQZMLBORDGWNPD-UHFFFAOYSA-N N-iodosuccinimide Chemical compound IN1C(=O)CCC1=O LQZMLBORDGWNPD-UHFFFAOYSA-N 0.000 description 8
• PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 8
• 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 8
• 238000001035 drying Methods 0.000 description 8
• 229910052739 hydrogen Inorganic materials 0.000 description 8
• 239000001257 hydrogen Substances 0.000 description 8
• 229960004592 isopropanol Drugs 0.000 description 8
• 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 8
• LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 8
• 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 8
• VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 8
• FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 7
• 239000012359 Methanesulfonyl chloride Substances 0.000 description 7
• WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 7
• FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 7
• 125000003710 aryl alkyl group Chemical group 0.000 description 7
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
• KVVMXWRFYAGASO-UHFFFAOYSA-N azetidine-1-carboxylic acid Chemical compound OC(=O)N1CCC1 KVVMXWRFYAGASO-UHFFFAOYSA-N 0.000 description 7
• 239000003054 catalyst Substances 0.000 description 7
• 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 7
• 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 7
• QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 7
• 239000012299 nitrogen atmosphere Substances 0.000 description 7
• VVWRJUBEIPHGQF-MDZDMXLPSA-N propan-2-yl (ne)-n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)\N=N\C(=O)OC(C)C VVWRJUBEIPHGQF-MDZDMXLPSA-N 0.000 description 7
• 125000004076 pyridyl group Chemical group 0.000 description 7
• 102000016914 ras Proteins Human genes 0.000 description 7
• 125000006274 (C1-C3)alkoxy group Chemical group 0.000 description 6
• OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 6
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
• DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 6
• 239000000654 additive Substances 0.000 description 6
• 239000003513 alkali Substances 0.000 description 6
• 125000004448 alkyl carbonyl group Chemical group 0.000 description 6
• NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 6
• 229910052751 metal Inorganic materials 0.000 description 6
• 239000002184 metal Substances 0.000 description 6
• 239000012046 mixed solvent Substances 0.000 description 6
• 229910000160 potassium phosphate Inorganic materials 0.000 description 6
• 235000011009 potassium phosphates Nutrition 0.000 description 6
• FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 6
• JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 6
• DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 6
• FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 6
• 125000001412 tetrahydropyranyl group Chemical group 0.000 description 6
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 6
• 229930195735 unsaturated hydrocarbon Natural products 0.000 description 6
• 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 5
• 239000005909 Kieselgur Substances 0.000 description 5
• FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 5
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
• 125000004423 acyloxy group Chemical group 0.000 description 5
• 125000004453 alkoxycarbonyl group Chemical group 0.000 description 5
• 150000001408 amides Chemical class 0.000 description 5
• 125000002619 bicyclic group Chemical group 0.000 description 5
• 239000012267 brine Substances 0.000 description 5
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• LODBDUJPJKPKCY-UHFFFAOYSA-N N-(5-tert-butyl-2-chloro-4-methylphenyl)acetamide Chemical compound CC1=CC(=C(C=C1C(C)(C)C)NC(=O)C)Cl LODBDUJPJKPKCY-UHFFFAOYSA-N 0.000 description 2
• AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 description 2
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• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
• DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
• 150000001299 aldehydes Chemical class 0.000 description 2
• 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
• 125000000278 alkyl amino alkyl group Chemical group 0.000 description 2
• 125000005196 alkyl carbonyloxy group Chemical group 0.000 description 2
• 238000007112 amidation reaction Methods 0.000 description 2
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• BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
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• 230000000259 anti-tumor effect Effects 0.000 description 2
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• 125000005098 aryl alkoxy carbonyl group Chemical group 0.000 description 2
• 125000005199 aryl carbonyloxy group Chemical group 0.000 description 2
• 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
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• 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 2
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• 239000002738 chelating agent Substances 0.000 description 2
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• 239000013078 crystal Substances 0.000 description 2
• 230000008025 crystallization Effects 0.000 description 2
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• 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
• 125000000062 cyclohexylmethoxy group Chemical group [H]C([H])(O*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
• 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
• 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 description 2
• 238000010511 deprotection reaction Methods 0.000 description 2
• 125000004663 dialkyl amino group Chemical group 0.000 description 2
• AGCOMFFHXJMNLN-UHFFFAOYSA-N dichloromethane;dihydrochloride Chemical compound Cl.Cl.ClCCl AGCOMFFHXJMNLN-UHFFFAOYSA-N 0.000 description 2
• 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 2
• UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 2
• MLYMKNBAQUPBOO-UHFFFAOYSA-N dimethyl 1-propan-2-ylimidazole-4,5-dicarboxylate Chemical compound COC(=O)C=1N=CN(C(C)C)C=1C(=O)OC MLYMKNBAQUPBOO-UHFFFAOYSA-N 0.000 description 2
• XBIPBYUBAYFWLY-UHFFFAOYSA-N dimethyl 2-bromo-1-methylimidazole-4,5-dicarboxylate Chemical compound BrC=1N(C(=C(N1)C(=O)OC)C(=O)OC)C XBIPBYUBAYFWLY-UHFFFAOYSA-N 0.000 description 2
• JMQGGPRJQOQKRT-UHFFFAOYSA-N diphenyl hydrogen phosphate;azide Chemical compound [N-]=[N+]=[N-].C=1C=CC=CC=1OP(=O)(O)OC1=CC=CC=C1 JMQGGPRJQOQKRT-UHFFFAOYSA-N 0.000 description 2
• GPAYUJZHTULNBE-UHFFFAOYSA-N diphenylphosphine Chemical compound C=1C=CC=CC=1PC1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-N 0.000 description 2
• 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 2
• YVJZJAJAGZNKMY-UHFFFAOYSA-N ethyl 2-bromo-3-propan-2-yl-5-(trifluoromethyl)imidazole-4-carboxylate Chemical compound CCOC(=O)C1=C(N=C(N1C(C)C)Br)C(F)(F)F YVJZJAJAGZNKMY-UHFFFAOYSA-N 0.000 description 2
• OBFIZSPFBNULEK-UHFFFAOYSA-N ethyl 2-ethenyl-3-propan-2-yl-5-(trifluoromethyl)imidazole-4-carboxylate Chemical compound CCOC(=O)C1=C(N=C(N1C(C)C)C=C)C(F)(F)F OBFIZSPFBNULEK-UHFFFAOYSA-N 0.000 description 2
• ZRDOKPWVBHDGHJ-UHFFFAOYSA-N ethyl 3-cyclopropyl-5-methylimidazole-4-carboxylate Chemical compound CCOC(=O)C1=C(N=CN1C2CC2)C ZRDOKPWVBHDGHJ-UHFFFAOYSA-N 0.000 description 2
• SQOGOQOITFUZNT-UHFFFAOYSA-N ethyl 4-chloro-2,5-dimethylpyrazole-3-carboxylate Chemical compound CCOC(=O)C1=C(Cl)C(C)=NN1C SQOGOQOITFUZNT-UHFFFAOYSA-N 0.000 description 2
• FNFMBVQIFWBJPN-UHFFFAOYSA-N ethyl 4-cyano-1h-imidazole-5-carboxylate Chemical compound CCOC(=O)C=1NC=NC=1C#N FNFMBVQIFWBJPN-UHFFFAOYSA-N 0.000 description 2
• WUWBXROZAMCTTN-UHFFFAOYSA-N ethyl 5-(bromomethyl)-4-chloro-2-methylpyrazole-3-carboxylate Chemical compound CCOC(=O)C1=C(C(=NN1C)CBr)Cl WUWBXROZAMCTTN-UHFFFAOYSA-N 0.000 description 2
• WYCYKJRUORMBEE-UHFFFAOYSA-N ethyl 5-methyl-3-propan-2-ylimidazole-4-carboxylate Chemical compound CCOC(=O)c1c(C)ncn1C(C)C WYCYKJRUORMBEE-UHFFFAOYSA-N 0.000 description 2
• 229960003750 ethyl chloride Drugs 0.000 description 2
• 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 2
• 238000001914 filtration Methods 0.000 description 2
• 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 description 2
• 230000009454 functional inhibition Effects 0.000 description 2
• 125000002541 furyl group Chemical group 0.000 description 2
• 210000004211 gastric acid Anatomy 0.000 description 2
• 239000011521 glass Substances 0.000 description 2
• 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 description 2
• 125000004438 haloalkoxy group Chemical group 0.000 description 2
• 230000002140 halogenating effect Effects 0.000 description 2
• 125000001072 heteroaryl group Chemical group 0.000 description 2
• 150000004678 hydrides Chemical class 0.000 description 2
• 230000007062 hydrolysis Effects 0.000 description 2
• XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
• 125000002632 imidazolidinyl group Chemical group 0.000 description 2
• PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
• INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
• 239000007951 isotonicity adjuster Substances 0.000 description 2
• 150000002576 ketones Chemical class 0.000 description 2
• YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 2
• KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
• ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 2
• 239000000314 lubricant Substances 0.000 description 2
• 201000005202 lung cancer Diseases 0.000 description 2
• 208000015486 malignant pancreatic neoplasm Diseases 0.000 description 2
• 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 2
• UUKJSJIBRZCCPV-UHFFFAOYSA-N methyl 2,5-diiodo-3-methylimidazole-4-carboxylate Chemical compound COC(=O)C=1N(C(=NC1I)I)C UUKJSJIBRZCCPV-UHFFFAOYSA-N 0.000 description 2
• OHAIIBYBMSUMSS-UHFFFAOYSA-N methyl 2-(1-acetyloxyethenyl)-3-methylimidazole-4-carboxylate Chemical compound CC(=O)OC(=C)C1=NC=C(N1C)C(=O)OC OHAIIBYBMSUMSS-UHFFFAOYSA-N 0.000 description 2
• PRRPUSNWDRPKLK-UHFFFAOYSA-N methyl 2-(1-chloroethyl)-3-methylimidazole-4-carboxylate Chemical compound CC(C1=NC=C(N1C)C(=O)OC)Cl PRRPUSNWDRPKLK-UHFFFAOYSA-N 0.000 description 2
• FYDLECIKUFOCJR-UHFFFAOYSA-N methyl 2-(1-hydroxyethyl)-3-methylimidazole-4-carboxylate Chemical compound OC(C)C1=NC=C(N1C)C(=O)OC FYDLECIKUFOCJR-UHFFFAOYSA-N 0.000 description 2
• OCBHDOMBVDQIEZ-UHFFFAOYSA-N methyl 2-acetyl-3-methylimidazole-4-carboxylate Chemical compound C(C)(=O)C1=NC=C(N1C)C(=O)OC OCBHDOMBVDQIEZ-UHFFFAOYSA-N 0.000 description 2
• SMXZXTSYEHMIJQ-UHFFFAOYSA-N methyl 2-bromo-5-(difluoromethyl)-3-methylimidazole-4-carboxylate Chemical compound CN1C(=C(N=C1Br)C(F)F)C(=O)OC SMXZXTSYEHMIJQ-UHFFFAOYSA-N 0.000 description 2
• MGAWGVXMGWEQDC-UHFFFAOYSA-N methyl 2-bromo-5-formyl-3-methylimidazole-4-carboxylate Chemical compound CN1C(=C(N=C1Br)C=O)C(=O)OC MGAWGVXMGWEQDC-UHFFFAOYSA-N 0.000 description 2
• SWLCZEZEPBYTMD-UHFFFAOYSA-N methyl 2-ethenyl-5-iodo-3-methylimidazole-4-carboxylate Chemical compound CN1C(=NC(=C1C(=O)OC)I)C=C SWLCZEZEPBYTMD-UHFFFAOYSA-N 0.000 description 2
• XSVVORFWPGPINR-UHFFFAOYSA-N methyl 2-formyl-3-methylimidazole-4-carboxylate Chemical compound COC(=O)C1=CN=C(C=O)N1C XSVVORFWPGPINR-UHFFFAOYSA-N 0.000 description 2
• HFRPGNOJUJZFKS-UHFFFAOYSA-N methyl 5-(difluoromethyl)-3-propan-2-ylimidazole-4-carboxylate Chemical compound COC(=O)C1=C(N=CN1C(C)C)C(F)F HFRPGNOJUJZFKS-UHFFFAOYSA-N 0.000 description 2
• KCHYHLLGPDNORK-UHFFFAOYSA-N methyl 5-chloro-2-formyl-3-methylimidazole-4-carboxylate Chemical compound CN1C(=NC(=C1C(=O)OC)Cl)C=O KCHYHLLGPDNORK-UHFFFAOYSA-N 0.000 description 2
• AYOKWZVUNXLHJR-UHFFFAOYSA-N methyl 5-chloro-3-methylimidazole-4-carboxylate Chemical compound N1(C)C=NC(=C1C(=O)OC)Cl AYOKWZVUNXLHJR-UHFFFAOYSA-N 0.000 description 2
• DKVMACIFGOENFJ-UHFFFAOYSA-N methyl 5-fluoro-1h-imidazole-4-carboxylate Chemical compound COC(=O)C=1N=CNC=1F DKVMACIFGOENFJ-UHFFFAOYSA-N 0.000 description 2
• IDRNZLYHSBNEQM-UHFFFAOYSA-N methyl 5-formyl-3-propan-2-ylimidazole-4-carboxylate Chemical compound CC(C)N1C=NC(=C1C(=O)OC)C=O IDRNZLYHSBNEQM-UHFFFAOYSA-N 0.000 description 2
• WFJRIDQGVSJLLH-UHFFFAOYSA-N methyl n-aminocarbamate Chemical compound COC(=O)NN WFJRIDQGVSJLLH-UHFFFAOYSA-N 0.000 description 2
• 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 2
• XTCIWRDRDQTIKK-UHFFFAOYSA-N n-(5-tert-butyl-2-chlorophenyl)acetamide Chemical compound CC(=O)NC1=CC(C(C)(C)C)=CC=C1Cl XTCIWRDRDQTIKK-UHFFFAOYSA-N 0.000 description 2
• QUQLDSFMMZCQHF-UHFFFAOYSA-N n-(6-chloro-1h-indazol-3-yl)acetamide Chemical compound ClC1=CC=C2C(NC(=O)C)=NNC2=C1 QUQLDSFMMZCQHF-UHFFFAOYSA-N 0.000 description 2
• 125000001624 naphthyl group Chemical group 0.000 description 2
• 150000002829 nitrogen Chemical group 0.000 description 2
• 239000002773 nucleotide Substances 0.000 description 2
• 125000003729 nucleotide group Chemical group 0.000 description 2
• 125000002971 oxazolyl group Chemical group 0.000 description 2
• KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 2
• YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 2
• 201000002528 pancreatic cancer Diseases 0.000 description 2
• 208000008443 pancreatic carcinoma Diseases 0.000 description 2
• 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 2
• 239000000546 pharmaceutical excipient Substances 0.000 description 2
• HXITXNWTGFUOAU-UHFFFAOYSA-N phenylboronic acid Chemical compound OB(O)C1=CC=CC=C1 HXITXNWTGFUOAU-UHFFFAOYSA-N 0.000 description 2
• UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 2
• 230000004962 physiological condition Effects 0.000 description 2
• NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 2
• LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 2
• 239000002244 precipitate Substances 0.000 description 2
• 230000002265 prevention Effects 0.000 description 2
• 239000000651 prodrug Substances 0.000 description 2
• 229940002612 prodrug Drugs 0.000 description 2
• 239000000047 product Substances 0.000 description 2
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
• 239000012264 purified product Substances 0.000 description 2
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• 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 2
• 230000009467 reduction Effects 0.000 description 2
• 229930195734 saturated hydrocarbon Natural products 0.000 description 2
• RWGNEOUYYQBMEW-UHFFFAOYSA-M sodium 2-formyl-3-methylimidazole-4-carboxylate Chemical compound CN1C(=CN=C1C=O)C(=O)[O-].[Na+] RWGNEOUYYQBMEW-UHFFFAOYSA-M 0.000 description 2
• 239000012279 sodium borohydride Substances 0.000 description 2
• 229910000033 sodium borohydride Inorganic materials 0.000 description 2
• QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 2
• 235000009518 sodium iodide Nutrition 0.000 description 2
• 235000011006 sodium potassium tartrate Nutrition 0.000 description 2
• 238000003797 solvolysis reaction Methods 0.000 description 2
• 239000003381 stabilizer Substances 0.000 description 2
• 239000000829 suppository Substances 0.000 description 2
• GVMGNVGDJJVIGC-YUMQZZPRSA-N tert-butyl (3R,4R)-3-azido-4-(hydroxymethyl)pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@H]([C@H](C1)N=[N+]=[N-])CO GVMGNVGDJJVIGC-YUMQZZPRSA-N 0.000 description 2
• PBRXHMHVWRYNFE-NXEZZACHSA-N tert-butyl (3R,4S)-3-(cyanomethyl)-4-methylsulfonyloxypyrrolidine-1-carboxylate Chemical compound C(C)(C)(C)OC(=O)N1C[C@H]([C@@H](C1)OS(=O)(=O)C)CC#N PBRXHMHVWRYNFE-NXEZZACHSA-N 0.000 description 2
• ZLASHXUGBCPHRL-HTQZYQBOSA-N tert-butyl (3R,4S)-3-(fluoromethyl)-4-hydroxypyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@H]([C@@H](C1)O)CF ZLASHXUGBCPHRL-HTQZYQBOSA-N 0.000 description 2
• NHBVZYSVYLSKRA-RKDXNWHRSA-N tert-butyl (3R,4S)-3-(fluoromethyl)-4-methylsulfonyloxypyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@H]([C@@H](C1)OS(=O)(=O)C)CF NHBVZYSVYLSKRA-RKDXNWHRSA-N 0.000 description 2
• BSTWKRUNXOFBPE-JGVFFNPUSA-N tert-butyl (3s,4s)-3-hydroxy-4-(hydroxymethyl)pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1C[C@@H](O)[C@H](CO)C1 BSTWKRUNXOFBPE-JGVFFNPUSA-N 0.000 description 2
• LPUKFFKAQFBJRK-UHFFFAOYSA-N tert-butyl 3,5-dimethylimidazole-4-carboxylate Chemical compound CN1C=NC(=C1C(=O)OC(C)(C)C)C LPUKFFKAQFBJRK-UHFFFAOYSA-N 0.000 description 2
• AAIYEZMDRXEENN-UHFFFAOYSA-N tert-butyl 5-fluoro-3-methylimidazole-4-carboxylate Chemical compound CC(C)(C)OC(=O)C1=C(N=CN1C)F AAIYEZMDRXEENN-UHFFFAOYSA-N 0.000 description 2
• HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 2
• 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 2
• CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 2
• FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
• 239000008096 xylene Substances 0.000 description 2
• GTLDTDOJJJZVBW-UHFFFAOYSA-N zinc cyanide Chemical compound [Zn+2].N#[C-].N#[C-] GTLDTDOJJJZVBW-UHFFFAOYSA-N 0.000 description 2
• JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 description 1
• BJHATSCXXDIEIF-UHFFFAOYSA-N (1,5-dimethylimidazol-2-yl)methanol Chemical compound CC1=CN=C(CO)N1C BJHATSCXXDIEIF-UHFFFAOYSA-N 0.000 description 1
• 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
• 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 description 1
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
• 125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 1
• 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 description 1
• 125000004754 (C2-C12) dialkylamino group Chemical group 0.000 description 1
• 125000006717 (C3-C10) cycloalkenyl group Chemical group 0.000 description 1
• 125000006736 (C6-C20) aryl group Chemical group 0.000 description 1
• MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 description 1
• YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
• GWLWDTKPKQMLRH-UHFFFAOYSA-N 1,3-dimethylimidazolidin-1-ium;chloride Chemical compound [Cl-].CN1CC[NH+](C)C1 GWLWDTKPKQMLRH-UHFFFAOYSA-N 0.000 description 1
• IBXMKLPFLZYRQZ-UHFFFAOYSA-N 1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1C=CC(=O)C=CC1=CC=CC=C1 IBXMKLPFLZYRQZ-UHFFFAOYSA-N 0.000 description 1
• BPPVVYPZWKVZFH-UHFFFAOYSA-N 1-(4-amino-3,3-difluoropyrrolidin-1-yl)prop-2-en-1-one 2,2,2-trifluoroacetic acid Chemical compound C=CC(=O)N1CC(C(C1)(F)F)N.C(=O)(C(F)(F)F)O BPPVVYPZWKVZFH-UHFFFAOYSA-N 0.000 description 1
• QGAWBPXVLZTBOF-FJXQXJEOSA-N 1-[(7R)-7-amino-5-azaspiro[2.4]heptan-5-yl]prop-2-en-1-one 2,2,2-trifluoroacetic acid Chemical compound C=CC(N(C1)CC2(CC2)[C@H]1N)=O.OC(C(F)(F)F)=O QGAWBPXVLZTBOF-FJXQXJEOSA-N 0.000 description 1
• XHCAGOVGSDHHNP-UHFFFAOYSA-N 1-bromo-4-tert-butylbenzene Chemical compound CC(C)(C)C1=CC=C(Br)C=C1 XHCAGOVGSDHHNP-UHFFFAOYSA-N 0.000 description 1
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