NO309191B1 - Eterderivater, anvendelse derav og farmasöytisk blanding - Google Patents

Info

Publication number

NO309191B1

NO309191B1 NO954321A NO954321A NO309191B1 NO 309191 B1 NO309191 B1 NO 309191B1 NO 954321 A NO954321 A NO 954321A NO 954321 A NO954321 A NO 954321A NO 309191 B1 NO309191 B1 NO 309191B1

Authority

NO

Norway

Prior art keywords

methyl

oxo

hydroxy

tetrahydroquinolin

mixture

Prior art date

1993-04-29

Links

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• 150000002170 ethers Chemical class 0.000 title claims abstract description 30
• 239000008194 pharmaceutical composition Substances 0.000 title abstract description 3
• -1 oxy, thio, sulfinyl Chemical group 0.000 claims abstract description 160
• 150000003839 salts Chemical class 0.000 claims abstract description 32
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 28
• 238000002360 preparation method Methods 0.000 claims abstract description 27
• 239000001257 hydrogen Substances 0.000 claims abstract description 20
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 20
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 19
• 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims abstract description 16
• 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims abstract description 14
• 125000001589 carboacyl group Chemical group 0.000 claims abstract description 10
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 7
• 125000001634 furandiyl group Chemical group O1C(=C(C=C1)*)* 0.000 claims abstract description 4
• 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 claims abstract description 4
• 239000000203 mixture Substances 0.000 claims description 262
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 26
• 125000001424 substituent group Chemical group 0.000 claims description 23
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 13
• 150000002617 leukotrienes Chemical class 0.000 claims description 13
• 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 13
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
• 201000010099 disease Diseases 0.000 claims description 10
• 229910052757 nitrogen Inorganic materials 0.000 claims description 10
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 10
• DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 claims description 9
• 229910052736 halogen Inorganic materials 0.000 claims description 9
• 150000002367 halogens Chemical class 0.000 claims description 9
• 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 claims description 8
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 8
• 239000000460 chlorine Substances 0.000 claims description 8
• 229910052801 chlorine Inorganic materials 0.000 claims description 8
• 229910052731 fluorine Inorganic materials 0.000 claims description 8
• 239000011737 fluorine Substances 0.000 claims description 8
• 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 7
• 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 7
• 125000003282 alkyl amino group Chemical group 0.000 claims description 7
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
• MQLADKMVHOOVET-HXPMCKFVSA-N 5-[4-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]thiophen-2-yl]sulfanyl-1-methyl-3h-indol-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CSC(SC=2C=C3CC(=O)N(C)C3=CC=2)=C1 MQLADKMVHOOVET-HXPMCKFVSA-N 0.000 claims description 6
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
• 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 6
• 239000003085 diluting agent Substances 0.000 claims description 6
• 229910052760 oxygen Inorganic materials 0.000 claims description 6
• 239000001301 oxygen Chemical group 0.000 claims description 6
• CKMCERYYKCTVTC-RNODOKPDSA-N 6-[4-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]thiophen-2-yl]sulfanyl-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CSC(SC=2C=C3CCC(=O)N(C)C3=CC=2)=C1 CKMCERYYKCTVTC-RNODOKPDSA-N 0.000 claims description 5
• GQMXJDTXYOYLQO-HXPMCKFVSA-N 6-[[5-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]-1,3-thiazol-2-yl]sulfanyl]-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C(S1)=CN=C1SC1=CC=C(N(C)C(=O)CC2)C2=C1 GQMXJDTXYOYLQO-HXPMCKFVSA-N 0.000 claims description 5
• 239000005864 Sulphur Chemical group 0.000 claims description 5
• 125000003545 alkoxy group Chemical group 0.000 claims description 5
• 125000005842 heteroatom Chemical group 0.000 claims description 5
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 5
• GKEXXHZCNJWHTP-QMHKHESXSA-N 1-ethyl-6-[3-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]phenyl]sulfanyl-3,4-dihydroquinolin-2-one Chemical compound C=1C=C2N(CC)C(=O)CCC2=CC=1SC(C=1)=CC=CC=1[C@@]1(O)CCO[C@@H](C)C1 GKEXXHZCNJWHTP-QMHKHESXSA-N 0.000 claims description 4
• WSCKJOLBZOVPOQ-RCDICMHDSA-N 6-[3-fluoro-5-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]phenyl]sulfanyl-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CC(F)=CC(SC=2C=C3CCC(=O)N(C)C3=CC=2)=C1 WSCKJOLBZOVPOQ-RCDICMHDSA-N 0.000 claims description 4
• 125000003342 alkenyl group Chemical group 0.000 claims description 4
• 125000001153 fluoro group Chemical group F* 0.000 claims description 4
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
• WOPIQWCZYABHQK-LHSJRXKWSA-N 5-[3-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]phenyl]sulfanyl-1-methyl-3h-indol-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CC=CC(SC=2C=C3CC(=O)N(C)C3=CC=2)=C1 WOPIQWCZYABHQK-LHSJRXKWSA-N 0.000 claims description 3
• GOTQIPUFGWBLJX-BBATYDOGSA-N 5-[[5-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]-1,3-thiazol-2-yl]sulfanyl]-1-methyl-3h-indol-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C(S1)=CN=C1SC1=CC=C(N(C)C(=O)C2)C2=C1 GOTQIPUFGWBLJX-BBATYDOGSA-N 0.000 claims description 3
• VAABKGFNIQTLQB-OYHNWAKOSA-N 6-[3-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]phenyl]sulfanyl-1-methylquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CC=CC(SC=2C=C3C=CC(=O)N(C)C3=CC=2)=C1 VAABKGFNIQTLQB-OYHNWAKOSA-N 0.000 claims description 3
• RWKXBEHOMLLEIM-OYHNWAKOSA-N 6-[3-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]phenyl]sulfonyl-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CC=CC(S(=O)(=O)C=2C=C3CCC(=O)N(C)C3=CC=2)=C1 RWKXBEHOMLLEIM-OYHNWAKOSA-N 0.000 claims description 3
• BWJJUQBSWJSPAA-RCDICMHDSA-N 6-[3-fluoro-5-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]phenyl]sulfonyl-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CC(F)=CC(S(=O)(=O)C=2C=C3CCC(=O)N(C)C3=CC=2)=C1 BWJJUQBSWJSPAA-RCDICMHDSA-N 0.000 claims description 3
• UWDHQYJVHPCTHK-RNODOKPDSA-N 6-[4-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]thiophen-2-yl]sulfanyl-1-methylquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CSC(SC=2C=C3C=CC(=O)N(C)C3=CC=2)=C1 UWDHQYJVHPCTHK-RNODOKPDSA-N 0.000 claims description 3
• QNTFOXDXKBAGJN-RNODOKPDSA-N 6-[4-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]thiophen-2-yl]sulfonyl-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CSC(S(=O)(=O)C=2C=C3CCC(=O)N(C)C3=CC=2)=C1 QNTFOXDXKBAGJN-RNODOKPDSA-N 0.000 claims description 3
• PWQLVCDGHZUJFG-HXPMCKFVSA-N 6-[[5-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]-1,3-thiazol-2-yl]sulfonyl]-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CN=C(S(=O)(=O)C=2C=C3CCC(=O)N(C)C3=CC=2)S1 PWQLVCDGHZUJFG-HXPMCKFVSA-N 0.000 claims description 3
• 125000000304 alkynyl group Chemical group 0.000 claims description 3
• 125000004043 oxo group Chemical group O=* 0.000 claims description 3
• 125000000464 thioxo group Chemical group S=* 0.000 claims description 3
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
• HOGWMNMBODEHQP-UHFFFAOYSA-N 7-fluoro-6-[4-(4-hydroxy-2-methyloxan-4-yl)thiophen-2-yl]sulfanyl-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1COC(C)CC1(O)C1=CSC(SC=2C(=CC=3N(C)C(=O)CCC=3C=2)F)=C1 HOGWMNMBODEHQP-UHFFFAOYSA-N 0.000 claims description 2
• KGDCDDGNZTYFSR-JEOXALJRSA-N 7-fluoro-6-[[5-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]-1,3-thiazol-2-yl]sulfanyl]-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C(S1)=CN=C1SC(C(=C1)F)=CC2=C1N(C)C(=O)CC2 KGDCDDGNZTYFSR-JEOXALJRSA-N 0.000 claims description 2
• RVVPQOMDRCJWAW-RCDICMHDSA-N 8-chloro-6-[3-[(2s,4r)-4-hydroxy-2-methyloxan-4-yl]phenyl]sulfanyl-1-methyl-3,4-dihydroquinolin-2-one Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CC=CC(SC=2C=C3CCC(=O)N(C)C3=C(Cl)C=2)=C1 RVVPQOMDRCJWAW-RCDICMHDSA-N 0.000 claims description 2
• 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
• 239000002547 new drug Substances 0.000 claims description 2
• 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 6
• YBDQLHBVNXARAU-UHFFFAOYSA-N 2-methyloxane Chemical compound CC1CCCCO1 YBDQLHBVNXARAU-UHFFFAOYSA-N 0.000 claims 1
• 238000000034 method Methods 0.000 abstract description 62
• 230000008569 process Effects 0.000 abstract description 2
• 229910052717 sulfur Inorganic materials 0.000 abstract description 2
• 239000011593 sulfur Substances 0.000 abstract description 2
• 239000000867 Lipoxygenase Inhibitor Substances 0.000 abstract 1
• 241001620634 Roger Species 0.000 abstract 1
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 222
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 183
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 129
• 239000000243 solution Substances 0.000 description 104
• 150000001875 compounds Chemical class 0.000 description 75
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 68
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 66
• 239000007858 starting material Substances 0.000 description 66
• 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 60
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 48
• 238000004440 column chromatography Methods 0.000 description 41
• 239000003480 eluent Substances 0.000 description 40
• 239000012267 brine Substances 0.000 description 38
• HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 38
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 36
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 34
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 30
• 239000012074 organic phase Substances 0.000 description 28
• 239000000463 material Substances 0.000 description 25
• 238000012360 testing method Methods 0.000 description 25
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 23
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 22
• UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 20
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
• NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 18
• MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 18
• 102100022364 Polyunsaturated fatty acid 5-lipoxygenase Human genes 0.000 description 18
• 239000011734 sodium Substances 0.000 description 18
• 101710156627 Polyunsaturated fatty acid 5-lipoxygenase Proteins 0.000 description 17
• 229920006395 saturated elastomer Polymers 0.000 description 17
• KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 16
• 239000003921 oil Substances 0.000 description 16
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 16
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 14
• CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 14
• 239000006260 foam Substances 0.000 description 13
• VNYSSYRCGWBHLG-AMOLWHMGSA-N leukotriene B4 Chemical compound CCCCC\C=C/C[C@@H](O)\C=C\C=C\C=C/[C@@H](O)CCCC(O)=O VNYSSYRCGWBHLG-AMOLWHMGSA-N 0.000 description 13
• 238000000746 purification Methods 0.000 description 13
• SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 12
• 239000002585 base Substances 0.000 description 11
• 238000006243 chemical reaction Methods 0.000 description 11
• YNMYGZQCCGUVOA-JOYOIKCWSA-N (2s,4r)-4-(3-iodophenyl)-2-methyloxan-4-ol Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CC=CC(I)=C1 YNMYGZQCCGUVOA-JOYOIKCWSA-N 0.000 description 10
• 229960000583 acetic acid Drugs 0.000 description 10
• 239000003054 catalyst Substances 0.000 description 10
• 230000000694 effects Effects 0.000 description 10
• 229910000030 sodium bicarbonate Inorganic materials 0.000 description 10
• 235000017557 sodium bicarbonate Nutrition 0.000 description 10
• FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 10
• JBFVGBROEBUKDK-OIBJUYFYSA-N (2s,4r)-2-methyl-4-(5-sulfanylthiophen-3-yl)oxan-4-ol Chemical compound C1CO[C@@H](C)C[C@@]1(O)C1=CSC(S)=C1 JBFVGBROEBUKDK-OIBJUYFYSA-N 0.000 description 9
• QYMYRURANOPZIX-UHFFFAOYSA-N 6-iodo-1-methyl-3,4-dihydroquinolin-2-one Chemical compound IC1=CC=C2N(C)C(=O)CCC2=C1 QYMYRURANOPZIX-UHFFFAOYSA-N 0.000 description 9
• 235000019270 ammonium chloride Nutrition 0.000 description 9
• KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
• 125000000623 heterocyclic group Chemical group 0.000 description 9
• 230000002401 inhibitory effect Effects 0.000 description 9
• NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 9
• 239000012258 stirred mixture Substances 0.000 description 9
• MQOPUXINXNVMKJ-YFKPBYRVSA-N (2s)-2-methyloxan-4-one Chemical compound C[C@H]1CC(=O)CCO1 MQOPUXINXNVMKJ-YFKPBYRVSA-N 0.000 description 8
• 241001465754 Metazoa Species 0.000 description 8
• KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 8
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
• YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 8
• 239000006185 dispersion Substances 0.000 description 8
• 239000012362 glacial acetic acid Substances 0.000 description 8
• 239000002480 mineral oil Substances 0.000 description 8
• 235000010446 mineral oil Nutrition 0.000 description 8
• 239000003208 petroleum Substances 0.000 description 8
• 229910000027 potassium carbonate Inorganic materials 0.000 description 8
• 235000011181 potassium carbonates Nutrition 0.000 description 8
• 239000012312 sodium hydride Substances 0.000 description 8
• 229910000104 sodium hydride Inorganic materials 0.000 description 8
• 125000004149 thio group Chemical group *S* 0.000 description 8
• WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 7
• 102000004005 Prostaglandin-endoperoxide synthases Human genes 0.000 description 7
• 108090000459 Prostaglandin-endoperoxide synthases Proteins 0.000 description 7
• 239000002253 acid Substances 0.000 description 7
• 238000005859 coupling reaction Methods 0.000 description 7
• 230000002757 inflammatory effect Effects 0.000 description 7
• 229910052943 magnesium sulfate Inorganic materials 0.000 description 7
• 235000019341 magnesium sulphate Nutrition 0.000 description 7
• 238000004519 manufacturing process Methods 0.000 description 7
• 239000000047 product Substances 0.000 description 7
• 238000010992 reflux Methods 0.000 description 7
• NYCDFHQOYLMAGZ-UHFFFAOYSA-N 1-methyl-6-sulfanyl-3,4-dihydroquinolin-2-one Chemical compound SC1=CC=C2N(C)C(=O)CCC2=C1 NYCDFHQOYLMAGZ-UHFFFAOYSA-N 0.000 description 6
• WARSUKBSFLACOI-UHFFFAOYSA-N 5-bromo-1-methyl-3h-indol-2-one Chemical compound BrC1=CC=C2N(C)C(=O)CC2=C1 WARSUKBSFLACOI-UHFFFAOYSA-N 0.000 description 6
• WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
• QZRGKCOWNLSUDK-UHFFFAOYSA-N Iodochlorine Chemical compound ICl QZRGKCOWNLSUDK-UHFFFAOYSA-N 0.000 description 6
• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
• DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 6
• 125000002252 acyl group Chemical group 0.000 description 6
• 230000015572 biosynthetic process Effects 0.000 description 6
• 239000003795 chemical substances by application Substances 0.000 description 6
• CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 6
• 239000003112 inhibitor Substances 0.000 description 6
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