CA2138264C - Preparation of compounds of lignan series - Google Patents
Preparation of compounds of lignan series Download PDFInfo
- Publication number
- CA2138264C CA2138264C CA002138264A CA2138264A CA2138264C CA 2138264 C CA2138264 C CA 2138264C CA 002138264 A CA002138264 A CA 002138264A CA 2138264 A CA2138264 A CA 2138264A CA 2138264 C CA2138264 C CA 2138264C
- Authority
- CA
- Canada
- Prior art keywords
- compound
- preparation
- synthesis
- reaction
- give
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 171
- 238000002360 preparation method Methods 0.000 title abstract description 83
- 229930013686 lignan Natural products 0.000 title abstract description 10
- 235000009408 lignans Nutrition 0.000 title abstract description 10
- 150000005692 lignans Chemical class 0.000 title abstract description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 118
- 238000000034 method Methods 0.000 claims abstract description 67
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 29
- -1 lactone compound Chemical class 0.000 claims abstract description 18
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 9
- 238000007259 addition reaction Methods 0.000 claims abstract description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 238000004519 manufacturing process Methods 0.000 claims abstract description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 125000005530 alkylenedioxy group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 125000004953 trihalomethyl group Chemical group 0.000 claims description 4
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 description 86
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 81
- 230000015572 biosynthetic process Effects 0.000 description 81
- 238000003786 synthesis reaction Methods 0.000 description 81
- 238000005160 1H NMR spectroscopy Methods 0.000 description 52
- 239000000243 solution Substances 0.000 description 51
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 46
- 238000002844 melting Methods 0.000 description 44
- 230000008018 melting Effects 0.000 description 44
- 239000000203 mixture Substances 0.000 description 44
- 101150041968 CDC13 gene Proteins 0.000 description 43
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 43
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 42
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 26
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 24
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 22
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 22
- 235000012000 cholesterol Nutrition 0.000 description 17
- 125000005594 diketone group Chemical group 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 238000004458 analytical method Methods 0.000 description 16
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 15
- 239000012267 brine Substances 0.000 description 15
- 239000012043 crude product Substances 0.000 description 15
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 238000001816 cooling Methods 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000000746 purification Methods 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- WGLUMOCWFMKWIL-UHFFFAOYSA-N dichloromethane;methanol Chemical compound OC.ClCCl WGLUMOCWFMKWIL-UHFFFAOYSA-N 0.000 description 6
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical compound [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 108010062497 VLDL Lipoproteins Proteins 0.000 description 5
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 4
- WMPDAIZRQDCGFH-UHFFFAOYSA-N 3-methoxybenzaldehyde Chemical compound COC1=CC=CC(C=O)=C1 WMPDAIZRQDCGFH-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- IMAKHNTVDGLIRY-UHFFFAOYSA-N methyl prop-2-ynoate Chemical compound COC(=O)C#C IMAKHNTVDGLIRY-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 4
- WJUFSDZVCOTFON-UHFFFAOYSA-N veratraldehyde Chemical compound COC1=CC=C(C=O)C=C1OC WJUFSDZVCOTFON-UHFFFAOYSA-N 0.000 description 4
- 239000001431 2-methylbenzaldehyde Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 238000008214 LDL Cholesterol Methods 0.000 description 3
- 235000019270 ammonium chloride Nutrition 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- FCZCIXQGZOUIDN-UHFFFAOYSA-N ethyl 2-diethoxyphosphinothioyloxyacetate Chemical compound CCOC(=O)COP(=S)(OCC)OCC FCZCIXQGZOUIDN-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 3
- 238000010898 silica gel chromatography Methods 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- VUDZSIYXZUYWSC-DBRKOABJSA-N (4r)-1-[(2r,4r,5r)-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-hydroxy-1,3-diazinan-2-one Chemical compound FC1(F)[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)N[C@H](O)CC1 VUDZSIYXZUYWSC-DBRKOABJSA-N 0.000 description 2
- AXQACEQYCPKDMV-RZAWKFBISA-N (4r,4as,7ar,12bs)-3-(cyclopropylmethyl)-4a,7,9-trihydroxy-n-[2-(3-phenyl-1,2,4-oxadiazol-5-yl)propan-2-yl]-1,2,4,5,7a,13-hexahydro-4,12-methanobenzofuro[3,2-e]isoquinoline-6-carboxamide Chemical compound N1([C@@H]2CC=3C4=C(C(=CC=3)O)O[C@H]3C(O)=C(C[C@]2(O)[C@]34CC1)C(=O)NC(C)(C)C=1ON=C(N=1)C=1C=CC=CC=1)CC1CC1 AXQACEQYCPKDMV-RZAWKFBISA-N 0.000 description 2
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical compound CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 2
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 0 COC(c1c(C(*)=O)c(O)c(cc(*)c(*)c2*)c2c1-c(cc1*)ccc1O*)=O Chemical compound COC(c1c(C(*)=O)c(O)c(cc(*)c(*)c2*)c2c1-c(cc1*)ccc1O*)=O 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- 150000001241 acetals Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- RBHJBMIOOPYDBQ-UHFFFAOYSA-N carbon dioxide;propan-2-one Chemical compound O=C=O.CC(C)=O RBHJBMIOOPYDBQ-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
- GRWVQDDAKZFPFI-UHFFFAOYSA-H chromium(III) sulfate Chemical compound [Cr+3].[Cr+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRWVQDDAKZFPFI-UHFFFAOYSA-H 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 229940125782 compound 2 Drugs 0.000 description 2
- 229940126214 compound 3 Drugs 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 238000011065 in-situ storage Methods 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
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- DQBHLLPGTJOYAT-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-3-(4-methoxybenzoyl)-4-oxonaphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=C(OC)C=C1 DQBHLLPGTJOYAT-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- BTFQKIATRPGRBS-UHFFFAOYSA-N o-tolualdehyde Chemical compound CC1=CC=CC=C1C=O BTFQKIATRPGRBS-UHFFFAOYSA-N 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 2
- FXLOVSHXALFLKQ-UHFFFAOYSA-N p-tolualdehyde Chemical compound CC1=CC=C(C=O)C=C1 FXLOVSHXALFLKQ-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- ISXOBTBCNRIIQO-UHFFFAOYSA-N tetrahydrothiophene 1-oxide Chemical compound O=S1CCCC1 ISXOBTBCNRIIQO-UHFFFAOYSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
- RANYXVFYAIGDFE-UHFFFAOYSA-N 1,2,3-trimethoxynaphthalene Chemical compound C1=CC=C2C(OC)=C(OC)C(OC)=CC2=C1 RANYXVFYAIGDFE-UHFFFAOYSA-N 0.000 description 1
- KEIFWROAQVVDBN-UHFFFAOYSA-N 1,2-dihydronaphthalene Chemical compound C1=CC=C2C=CCCC2=C1 KEIFWROAQVVDBN-UHFFFAOYSA-N 0.000 description 1
- OOSZCNKVJAVHJI-UHFFFAOYSA-N 1-[(4-fluorophenyl)methyl]piperazine Chemical compound C1=CC(F)=CC=C1CN1CCNCC1 OOSZCNKVJAVHJI-UHFFFAOYSA-N 0.000 description 1
- UNNGUFMVYQJGTD-UHFFFAOYSA-N 2-Ethylbutanal Chemical compound CCC(CC)C=O UNNGUFMVYQJGTD-UHFFFAOYSA-N 0.000 description 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 1
- KKKJYDOHVKIIQP-UHFFFAOYSA-N 2-[4-(3-chlorobenzoyl)phenoxy]-N-pyridin-3-ylacetamide Chemical compound ClC=1C=C(C(=O)C2=CC=C(OCC(=O)NC=3C=NC=CC=3)C=C2)C=CC=1 KKKJYDOHVKIIQP-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- FPYUJUBAXZAQNL-UHFFFAOYSA-N 2-chlorobenzaldehyde Chemical compound ClC1=CC=CC=C1C=O FPYUJUBAXZAQNL-UHFFFAOYSA-N 0.000 description 1
- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 1
- RVBUGGBMJDPOST-UHFFFAOYSA-N 2-thiobarbituric acid Chemical compound O=C1CC(=O)NC(=S)N1 RVBUGGBMJDPOST-UHFFFAOYSA-N 0.000 description 1
- BUHYMJLFRZAFBF-UHFFFAOYSA-N 3,4,5-trimethoxybenzoyl chloride Chemical compound COC1=CC(C(Cl)=O)=CC(OC)=C1OC BUHYMJLFRZAFBF-UHFFFAOYSA-N 0.000 description 1
- ZWUSBSHBFFPRNE-UHFFFAOYSA-N 3,4-dichlorobenzaldehyde Chemical compound ClC1=CC=C(C=O)C=C1Cl ZWUSBSHBFFPRNE-UHFFFAOYSA-N 0.000 description 1
- LEKGYQWLMUVRGY-UHFFFAOYSA-N 3-(3,4-dimethoxyphenyl)-4,5,6-trimethoxy-3h-2-benzofuran-1-one Chemical compound C1=C(OC)C(OC)=CC=C1C1C2=C(OC)C(OC)=C(OC)C=C2C(=O)O1 LEKGYQWLMUVRGY-UHFFFAOYSA-N 0.000 description 1
- DNTVJEMGHBIUMW-IBGZPJMESA-N 3-[[4-[(1s)-1-[3-(3,5-dichlorophenyl)-5-(6-methoxynaphthalen-2-yl)pyrazol-1-yl]ethyl]benzoyl]amino]propanoic acid Chemical compound C1([C@H](C)N2N=C(C=C2C2=CC3=CC=C(C=C3C=C2)OC)C=2C=C(Cl)C=C(Cl)C=2)=CC=C(C(=O)NCCC(O)=O)C=C1 DNTVJEMGHBIUMW-IBGZPJMESA-N 0.000 description 1
- MWDVCHRYCKXEBY-LBPRGKRZSA-N 3-chloro-n-[2-oxo-2-[[(1s)-1-phenylethyl]amino]ethyl]benzamide Chemical compound N([C@@H](C)C=1C=CC=CC=1)C(=O)CNC(=O)C1=CC=CC(Cl)=C1 MWDVCHRYCKXEBY-LBPRGKRZSA-N 0.000 description 1
- SRWILAKSARHZPR-UHFFFAOYSA-N 3-chlorobenzaldehyde Chemical compound ClC1=CC=CC(C=O)=C1 SRWILAKSARHZPR-UHFFFAOYSA-N 0.000 description 1
- HIJLVHXVBWTMEV-UHFFFAOYSA-N 3-ethylpentanal Chemical compound CCC(CC)CC=O HIJLVHXVBWTMEV-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- BEOBZEOPTQQELP-UHFFFAOYSA-N 4-(trifluoromethyl)benzaldehyde Chemical compound FC(F)(F)C1=CC=C(C=O)C=C1 BEOBZEOPTQQELP-UHFFFAOYSA-N 0.000 description 1
- 125000002999 4-(trifluoromethyl)benzoyl group Chemical group FC(C1=CC=C(C(=O)*)C=C1)(F)F 0.000 description 1
- JOFDSYLCZIHGGO-UHFFFAOYSA-N 4-[(4-cyclohexylphenyl)methyl-[2-[[5-(dimethylamino)naphthalen-1-yl]sulfonyl-methylamino]acetyl]amino]-2-hydroxybenzoic acid Chemical compound C1=CC=C2C(N(C)C)=CC=CC2=C1S(=O)(=O)N(C)CC(=O)N(C=1C=C(O)C(C(O)=O)=CC=1)CC(C=C1)=CC=C1C1CCCCC1 JOFDSYLCZIHGGO-UHFFFAOYSA-N 0.000 description 1
- AVPYQKSLYISFPO-UHFFFAOYSA-N 4-chlorobenzaldehyde Chemical compound ClC1=CC=C(C=O)C=C1 AVPYQKSLYISFPO-UHFFFAOYSA-N 0.000 description 1
- 229960000549 4-dimethylaminophenol Drugs 0.000 description 1
- NJEAJBBKRDXYPX-UHFFFAOYSA-N 4h-naphthalen-1-one Chemical compound C1=CC=C2C(=O)C=CCC2=C1 NJEAJBBKRDXYPX-UHFFFAOYSA-N 0.000 description 1
- HSQGOSNQFMJSAI-UHFFFAOYSA-N 5-(3,4-dimethoxyphenyl)-5h-furo[3,4-f][1,3]benzodioxol-7-one Chemical compound C1=C(OC)C(OC)=CC=C1C1C2=CC(OCO3)=C3C=C2C(=O)O1 HSQGOSNQFMJSAI-UHFFFAOYSA-N 0.000 description 1
- CSQUXTSIDQURDV-UHFFFAOYSA-N 6-bromo-1,3-benzodioxole-5-carbaldehyde Chemical compound C1=C(C=O)C(Br)=CC2=C1OCO2 CSQUXTSIDQURDV-UHFFFAOYSA-N 0.000 description 1
- 206010003210 Arteriosclerosis Diseases 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 108010069201 VLDL Cholesterol Proteins 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 208000011775 arteriosclerosis disease Diseases 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 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 1
- 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 1
- 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 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012039 electrophile Substances 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
- WDCDAAMJNUHOIY-UHFFFAOYSA-N ethyl acetate;2-propan-2-yloxypropane Chemical compound CCOC(C)=O.CC(C)OC(C)C WDCDAAMJNUHOIY-UHFFFAOYSA-N 0.000 description 1
- PFCHFHIRKBAQGU-UHFFFAOYSA-N ethyl n-propyl ketone Natural products CCCC(=O)CC PFCHFHIRKBAQGU-UHFFFAOYSA-N 0.000 description 1
- 229960002089 ferrous chloride Drugs 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- KDCIHNCMPUBDKT-UHFFFAOYSA-N hexane;propan-2-one Chemical compound CC(C)=O.CCCCCC KDCIHNCMPUBDKT-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- FUKUFMFMCZIRNT-UHFFFAOYSA-N hydron;methanol;chloride Chemical compound Cl.OC FUKUFMFMCZIRNT-UHFFFAOYSA-N 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- BYRPTKZOXNFFDB-UHFFFAOYSA-N lithium;bis(trimethylsilyl)azanide;oxolane Chemical compound [Li+].C1CCOC1.C[Si](C)(C)[N-][Si](C)(C)C BYRPTKZOXNFFDB-UHFFFAOYSA-N 0.000 description 1
- OVWYEQOVUDKZNU-UHFFFAOYSA-N m-tolualdehyde Chemical compound CC1=CC=CC(C=O)=C1 OVWYEQOVUDKZNU-UHFFFAOYSA-N 0.000 description 1
- YTYMWWAQBLLQJP-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-3-(3-methoxybenzoyl)-4-oxonaphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=CC(OC)=C1 YTYMWWAQBLLQJP-UHFFFAOYSA-N 0.000 description 1
- RTJZHFRZYWRJOB-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-3-(3-methylbenzoyl)-4-oxonaphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=CC(C)=C1 RTJZHFRZYWRJOB-UHFFFAOYSA-N 0.000 description 1
- WWKBHHZGTQVHGM-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-4-oxo-3-[4-(trifluoromethyl)benzoyl]naphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=C(C(F)(F)F)C=C1 WWKBHHZGTQVHGM-UHFFFAOYSA-N 0.000 description 1
- MFKWWYDUOSOGBD-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-3-(2-ethylbutanoyl)-1-hydroxy-6,7,8-trimethoxy-4-oxonaphthalene-2-carboxylate Chemical compound C12=C(OC)C(OC)=C(OC)C=C2C(=O)C(C(=O)C(CC)CC)=C(C(=O)OC)C1(O)C1=CC=C(OC)C(OC)=C1 MFKWWYDUOSOGBD-UHFFFAOYSA-N 0.000 description 1
- OPKWYUQDCQFFJZ-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-3-(2-ethylbutanoyl)-4-hydroxy-6,7,8-trimethoxynaphthalene-2-carboxylate Chemical compound COC(=O)C=1C(C(=O)C(CC)CC)=C(O)C2=CC(OC)=C(OC)C(OC)=C2C=1C1=CC=C(OC)C(OC)=C1 OPKWYUQDCQFFJZ-UHFFFAOYSA-N 0.000 description 1
- JXHPHQZJLLADAD-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-3-(3-ethylpentanoyl)-1-hydroxy-6,7,8-trimethoxy-4-oxonaphthalene-2-carboxylate Chemical compound C12=C(OC)C(OC)=C(OC)C=C2C(=O)C(C(=O)CC(CC)CC)=C(C(=O)OC)C1(O)C1=CC=C(OC)C(OC)=C1 JXHPHQZJLLADAD-UHFFFAOYSA-N 0.000 description 1
- YQHHBVCALVLEJG-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-4-hydroxy-6,7,8-trimethoxy-3-(2-methoxybenzoyl)naphthalene-2-carboxylate Chemical compound OC1=C2C=C(OC)C(OC)=C(OC)C2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=CC=C1OC YQHHBVCALVLEJG-UHFFFAOYSA-N 0.000 description 1
- GJYRSVWPANRUNT-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-4-hydroxy-6,7,8-trimethoxy-3-(2-methylbenzoyl)naphthalene-2-carboxylate Chemical compound OC1=C2C=C(OC)C(OC)=C(OC)C2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=CC=C1C GJYRSVWPANRUNT-UHFFFAOYSA-N 0.000 description 1
- NZJPLJIRKJSEII-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-4-hydroxy-6,7,8-trimethoxy-3-(3-methoxybenzoyl)naphthalene-2-carboxylate Chemical compound OC1=C2C=C(OC)C(OC)=C(OC)C2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=CC(OC)=C1 NZJPLJIRKJSEII-UHFFFAOYSA-N 0.000 description 1
- LCHVYRAYDDKNDJ-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-4-hydroxy-6,7,8-trimethoxy-3-(3-methylbenzoyl)naphthalene-2-carboxylate Chemical compound OC1=C2C=C(OC)C(OC)=C(OC)C2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=CC(C)=C1 LCHVYRAYDDKNDJ-UHFFFAOYSA-N 0.000 description 1
- LSQPGWAQLSSMTI-UHFFFAOYSA-N methyl 1-(3,4-dimethoxyphenyl)-4-hydroxy-6,7,8-trimethoxy-3-[4-(trifluoromethyl)benzoyl]naphthalene-2-carboxylate Chemical compound OC1=C2C=C(OC)C(OC)=C(OC)C2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=C(C(F)(F)F)C=C1 LSQPGWAQLSSMTI-UHFFFAOYSA-N 0.000 description 1
- CSKSADNCHJPUQE-UHFFFAOYSA-N methyl 3-(2-chlorobenzoyl)-1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-4-oxonaphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=CC=C1Cl CSKSADNCHJPUQE-UHFFFAOYSA-N 0.000 description 1
- MOXPLPBTUGFGON-UHFFFAOYSA-N methyl 3-(2-chlorobenzoyl)-1-(3,4-dimethoxyphenyl)-4-hydroxy-6,7,8-trimethoxynaphthalene-2-carboxylate Chemical compound OC1=C2C=C(OC)C(OC)=C(OC)C2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=CC=C1Cl MOXPLPBTUGFGON-UHFFFAOYSA-N 0.000 description 1
- LLPQJCHGVJMZPD-UHFFFAOYSA-N methyl 3-(3,4-dichlorobenzoyl)-1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-4-oxonaphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=C(Cl)C(Cl)=C1 LLPQJCHGVJMZPD-UHFFFAOYSA-N 0.000 description 1
- XIVCUAYFCGLJJF-UHFFFAOYSA-N methyl 3-(3,4-dichlorobenzoyl)-1-(3,4-dimethoxyphenyl)-4-hydroxy-6,7,8-trimethoxynaphthalene-2-carboxylate Chemical compound OC1=C2C=C(OC)C(OC)=C(OC)C2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=C(Cl)C(Cl)=C1 XIVCUAYFCGLJJF-UHFFFAOYSA-N 0.000 description 1
- ROJYYOHMPIYDEC-UHFFFAOYSA-N methyl 3-(3-chlorobenzoyl)-1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-4-oxonaphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=CC(Cl)=C1 ROJYYOHMPIYDEC-UHFFFAOYSA-N 0.000 description 1
- OUSWFPUVAAZANY-UHFFFAOYSA-N methyl 3-(3-chlorobenzoyl)-1-(3,4-dimethoxyphenyl)-4-hydroxy-6,7,8-trimethoxynaphthalene-2-carboxylate Chemical compound OC1=C2C=C(OC)C(OC)=C(OC)C2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=CC(Cl)=C1 OUSWFPUVAAZANY-UHFFFAOYSA-N 0.000 description 1
- ZSUIPTHJXRYZHX-UHFFFAOYSA-N methyl 3-(4-chlorobenzoyl)-1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-4-oxonaphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=C(Cl)C=C1 ZSUIPTHJXRYZHX-UHFFFAOYSA-N 0.000 description 1
- PXYYQECMPBRALQ-UHFFFAOYSA-N methyl 3-(cyclohexanecarbonyl)-1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-4-oxonaphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1CCCCC1 PXYYQECMPBRALQ-UHFFFAOYSA-N 0.000 description 1
- MPIFPVJOKMRUIW-UHFFFAOYSA-N methyl 3-benzoyl-1-(3,4-dimethoxyphenyl)-1-hydroxy-6,7,8-trimethoxy-4-oxonaphthalene-2-carboxylate Chemical compound O=C1C2=CC(OC)=C(OC)C(OC)=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=CC=C1 MPIFPVJOKMRUIW-UHFFFAOYSA-N 0.000 description 1
- KHBJOBLJLSXZSR-UHFFFAOYSA-N methyl 3-benzoyl-1-(3,4-dimethoxyphenyl)-4-hydroxy-6,7,8-trimethoxynaphthalene-2-carboxylate Chemical compound OC1=C2C=C(OC)C(OC)=C(OC)C2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=CC=C1 KHBJOBLJLSXZSR-UHFFFAOYSA-N 0.000 description 1
- KLJQQTNFQPUZKP-UHFFFAOYSA-N methyl 4-(2-chlorophenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=CC=C1Cl KLJQQTNFQPUZKP-UHFFFAOYSA-N 0.000 description 1
- MCGITOQTCIWHBJ-UHFFFAOYSA-N methyl 4-(2-methoxyphenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=CC=C1OC MCGITOQTCIWHBJ-UHFFFAOYSA-N 0.000 description 1
- VUYYICDTTRSBDV-UHFFFAOYSA-N methyl 4-(2-methylphenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=CC=C1C VUYYICDTTRSBDV-UHFFFAOYSA-N 0.000 description 1
- MZAOQXYPJIMZIY-UHFFFAOYSA-N methyl 4-(3,4-dichlorophenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=C(Cl)C(Cl)=C1 MZAOQXYPJIMZIY-UHFFFAOYSA-N 0.000 description 1
- RDPRCPXGDRGISQ-UHFFFAOYSA-N methyl 4-(3-chlorophenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=CC(Cl)=C1 RDPRCPXGDRGISQ-UHFFFAOYSA-N 0.000 description 1
- XFRQPCJUJIEIHY-UHFFFAOYSA-N methyl 4-(3-methoxyphenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=CC(OC)=C1 XFRQPCJUJIEIHY-UHFFFAOYSA-N 0.000 description 1
- SYQMBIPVJQARKU-UHFFFAOYSA-N methyl 4-(3-methylphenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=CC(C)=C1 SYQMBIPVJQARKU-UHFFFAOYSA-N 0.000 description 1
- ALNNWERTFHBQFA-UHFFFAOYSA-N methyl 4-(4-chlorophenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=C(Cl)C=C1 ALNNWERTFHBQFA-UHFFFAOYSA-N 0.000 description 1
- JKGUUADORVKPOJ-UHFFFAOYSA-N methyl 4-(4-methoxyphenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=C(OC)C=C1 JKGUUADORVKPOJ-UHFFFAOYSA-N 0.000 description 1
- KZEPKSJCKHRDKP-UHFFFAOYSA-N methyl 4-(4-methylphenyl)-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=C(C)C=C1 KZEPKSJCKHRDKP-UHFFFAOYSA-N 0.000 description 1
- PLBIDVBZBUCCFD-UHFFFAOYSA-N methyl 4-[4-(trifluoromethyl)phenyl]-4-trimethylsilyloxybut-2-ynoate Chemical compound COC(=O)C#CC(O[Si](C)(C)C)C1=CC=C(C(F)(F)F)C=C1 PLBIDVBZBUCCFD-UHFFFAOYSA-N 0.000 description 1
- JRUBUCYCDHVLEZ-UHFFFAOYSA-N methyl 4-cyclohexyl-4-hydroxybut-2-ynoate Chemical compound COC(=O)C#CC(O)C1CCCCC1 JRUBUCYCDHVLEZ-UHFFFAOYSA-N 0.000 description 1
- HTERTZZULNKIPD-UHFFFAOYSA-N methyl 4-cyclohexyl-4-oxobut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1CCCCC1 HTERTZZULNKIPD-UHFFFAOYSA-N 0.000 description 1
- SAZXSUIDPREHSA-UHFFFAOYSA-N methyl 4-oxo-4-[4-(trifluoromethyl)phenyl]but-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=C(C(F)(F)F)C=C1 SAZXSUIDPREHSA-UHFFFAOYSA-N 0.000 description 1
- MSRRBJSMBKEECW-UHFFFAOYSA-N methyl 4-oxo-4-phenylbut-2-ynoate Chemical compound COC(=O)C#CC(=O)C1=CC=CC=C1 MSRRBJSMBKEECW-UHFFFAOYSA-N 0.000 description 1
- YOTYGGPXSLPHGR-UHFFFAOYSA-N methyl 5-(3,4-dimethoxyphenyl)-5-hydroxy-8-oxo-7-[4-(trifluoromethyl)benzoyl]benzo[f][1,3]benzodioxole-6-carboxylate Chemical compound O=C1C2=CC=3OCOC=3C=C2C(C=2C=C(OC)C(OC)=CC=2)(O)C(C(=O)OC)=C1C(=O)C1=CC=C(C(F)(F)F)C=C1 YOTYGGPXSLPHGR-UHFFFAOYSA-N 0.000 description 1
- OVVXNTJKKAOGCO-UHFFFAOYSA-N methyl 5-ethyl-4-oxohept-2-ynoate Chemical compound CCC(CC)C(=O)C#CC(=O)OC OVVXNTJKKAOGCO-UHFFFAOYSA-N 0.000 description 1
- HTKITAGAGQHZGR-UHFFFAOYSA-N methyl 6-ethyl-4-oxooct-2-ynoate Chemical compound CCC(CC)CC(=O)C#CC(=O)OC HTKITAGAGQHZGR-UHFFFAOYSA-N 0.000 description 1
- VUCXVEMSVGJHBW-UHFFFAOYSA-N methyl 8-(3,4-dimethoxyphenyl)-4,5,6-trimethoxy-10-[4-(trifluoromethyl)benzoyl]-1-trimethylsilyloxy-11-oxatricyclo[6.2.1.02,7]undeca-2,4,6,9-tetraene-9-carboxylate Chemical compound C1=C(OC)C(OC)=C(OC)C2=C1C1(O[Si](C)(C)C)OC2(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=C(C(F)(F)F)C=C1 VUCXVEMSVGJHBW-UHFFFAOYSA-N 0.000 description 1
- GGCBZBAKJCXEDE-UHFFFAOYSA-N methyl 8-(3,4-dimethoxyphenyl)-5-hydroxy-6-[4-(trifluoromethyl)benzoyl]benzo[f][1,3]benzodioxole-7-carboxylate Chemical compound OC1=C2C=C3OCOC3=CC2=C(C=2C=C(OC)C(OC)=CC=2)C(C(=O)OC)=C1C(=O)C1=CC=C(C(F)(F)F)C=C1 GGCBZBAKJCXEDE-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
- RCSBCWXPGSPJNF-UHFFFAOYSA-N n-[4-[5-[3-chloro-4-(trifluoromethoxy)phenyl]-1,3,4-oxadiazol-2-yl]butyl]-4-(1,8-naphthyridin-2-yl)butanamide Chemical compound C1=C(Cl)C(OC(F)(F)F)=CC=C1C(O1)=NN=C1CCCCNC(=O)CCCC1=CC=C(C=CC=N2)C2=N1 RCSBCWXPGSPJNF-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- HBEDNENASUYMPO-LJQANCHMSA-N n-hydroxy-4-[[(2r)-3-oxo-2-(thiophen-2-ylmethyl)-2,4-dihydroquinoxalin-1-yl]methyl]benzamide Chemical compound C1=CC(C(=O)NO)=CC=C1CN1C2=CC=CC=C2NC(=O)[C@H]1CC1=CC=CS1 HBEDNENASUYMPO-LJQANCHMSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- 238000011587 new zealand white rabbit Methods 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- IUBQJLUDMLPAGT-UHFFFAOYSA-N potassium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([K])[Si](C)(C)C IUBQJLUDMLPAGT-UHFFFAOYSA-N 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- UKLNMMHNWFDKNT-UHFFFAOYSA-M sodium chlorite Chemical compound [Na+].[O-]Cl=O UKLNMMHNWFDKNT-UHFFFAOYSA-M 0.000 description 1
- 229960002218 sodium chlorite Drugs 0.000 description 1
- NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 description 1
- 229940074545 sodium dihydrogen phosphate dihydrate Drugs 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- WNQRNJDWRMNXCZ-UHFFFAOYSA-N sodium;bis(triethylsilyl)azanide Chemical compound [Na+].CC[Si](CC)(CC)[N-][Si](CC)(CC)CC WNQRNJDWRMNXCZ-UHFFFAOYSA-N 0.000 description 1
- DZHAYSANSDYBFE-UHFFFAOYSA-N sodium;diethylazanide Chemical compound [Na+].CC[N-]CC DZHAYSANSDYBFE-UHFFFAOYSA-N 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
- C07C69/94—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring of polycyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8994493 | 1993-04-16 | ||
| JP089944/1993 | 1993-04-16 | ||
| PCT/JP1994/000612 WO1994024087A1 (fr) | 1993-04-16 | 1994-04-12 | Procede pour produire un compose de lignane |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2138264A1 CA2138264A1 (en) | 1994-10-27 |
| CA2138264C true CA2138264C (en) | 2004-04-06 |
Family
ID=13984820
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002138264A Expired - Fee Related CA2138264C (en) | 1993-04-16 | 1994-04-12 | Preparation of compounds of lignan series |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US5488134A (cg-RX-API-DMAC10.html) |
| EP (1) | EP0646570B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JP3411036B2 (cg-RX-API-DMAC10.html) |
| KR (1) | KR100277242B1 (cg-RX-API-DMAC10.html) |
| CN (1) | CN1046937C (cg-RX-API-DMAC10.html) |
| AT (1) | ATE167662T1 (cg-RX-API-DMAC10.html) |
| AU (1) | AU666819B2 (cg-RX-API-DMAC10.html) |
| CA (1) | CA2138264C (cg-RX-API-DMAC10.html) |
| DE (1) | DE69411243T2 (cg-RX-API-DMAC10.html) |
| DK (1) | DK0646570T3 (cg-RX-API-DMAC10.html) |
| ES (1) | ES2119190T3 (cg-RX-API-DMAC10.html) |
| TW (1) | TW255886B (cg-RX-API-DMAC10.html) |
| WO (1) | WO1994024087A1 (cg-RX-API-DMAC10.html) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2121060C (en) * | 1993-04-16 | 2004-04-06 | Sachio Mori | Preparation of lignan analogues |
| US6268392B1 (en) | 1994-09-13 | 2001-07-31 | G. D. Searle & Co. | Combination therapy employing ileal bile acid transport inhibiting benzothiepines and HMG Co-A reductase inhibitors |
| US6642268B2 (en) | 1994-09-13 | 2003-11-04 | G.D. Searle & Co. | Combination therapy employing ileal bile acid transport inhibiting benzothipines and HMG Co-A reductase inhibitors |
| US6262277B1 (en) | 1994-09-13 | 2001-07-17 | G.D. Searle And Company | Intermediates and processes for the preparation of benzothiepines having activity as inhibitors of ileal bile acid transport and taurocholate uptake |
| KR100376281B1 (ko) * | 1995-12-26 | 2003-09-26 | 에스케이케미칼주식회사 | 리그난의 제조방법 |
| EP1026167B1 (en) | 1997-09-29 | 2003-03-05 | Meiji Seika Kaisha Ltd. | Tricyclic triazolobenzazepine derivatives, process for producing the same and antiallergic agents |
| WO2000038721A1 (en) | 1998-12-23 | 2000-07-06 | G.D. Searle Llc | Combinations of cholesteryl ester transfer protein inhibitors and nicotinic acid derivatives for cardiovascular indications |
| DE69908644T2 (de) | 1998-12-23 | 2004-05-13 | G.D. Searle Llc, Chicago | Kombnationen von cholesteryl ester transfer protein inhibitoren und gallensäure sequestriermitteln für kardiovaskuläre indikationen |
| PT1140188E (pt) | 1998-12-23 | 2003-10-31 | Searle Llc | Combinacoes de inibidores do transporte de acidos biliares do ileo e de inibidores da proteina de transferencia de esteres de colesterilo para doencas cardiovasculares. |
| WO2000038722A1 (en) | 1998-12-23 | 2000-07-06 | G.D. Searle & Co. | COMBINATIONS OF CHOLESTERYL ESTER TRANSFER PROTEIN INHIBITORS AND HMG CoA REDUCTASE INHIBITORS FOR CARDIOVASCULAR INDICATIONS |
| US6562860B1 (en) | 1998-12-23 | 2003-05-13 | G. D. Searle & Co. | Combinations of ileal bile acid transport inhibitors and bile acid sequestering agents for cardiovascular indications |
| MXPA01006472A (es) | 1998-12-23 | 2004-03-10 | Searle Llc | Combinaciones de inhibidores de transporte de acido biliar ileal y derivados de acido fibrico para indicaciones cardiovasculares. |
| AU776664B2 (en) | 1998-12-23 | 2004-09-16 | G.D. Searle Llc | Combinations of cholesteryl ester transfer protein inhibitors and fibric acid derivatives for cardiovascular indications |
| WO2001068096A2 (en) * | 2000-03-10 | 2001-09-20 | Pharmacia Corporation | Combination therapy for the prophylaxis and treatment of hyperlipidemic conditions and disorders |
| HK1052183A1 (zh) | 2000-03-10 | 2003-09-05 | Pharmacia Corporation | 制造tetrahydrobenzothiepines的方法 |
| US6740663B2 (en) | 2001-11-02 | 2004-05-25 | G.D. Searle, Llc | Mono- and di-fluorinated benzothiepine compounds as inhibitors of apical sodium co-dependent bile acid transport (ASBT) and taurocholate uptake |
| WO2003061604A2 (en) | 2002-01-17 | 2003-07-31 | Pharmacia Corporation | Novel alkyl/aryl hydroxy or keto thiepines. |
| GB0307918D0 (en) | 2003-04-05 | 2003-05-14 | Astrazeneca Ab | Therapeutic use |
| EP2575821B1 (en) | 2010-05-26 | 2015-08-12 | Satiogen Pharmaceuticals, Inc. | Bile acid recycling inhibitors and satiogens for treatment of diabetes, obesity, and inflammatory gastrointestinal conditions |
| CA2852957C (en) | 2011-10-28 | 2020-08-04 | Lumena Pharmaceuticals, Inc. | Bile acid recycling inhibitors for treatment of hypercholemia and cholestatic liver disease |
| JP6217938B2 (ja) | 2011-10-28 | 2017-10-25 | ルメナ ファーマシューティカルズ エルエルシー | 小児の胆汁うっ滞性肝疾患の処置のための胆汁酸再循環阻害剤 |
| EP2968262A1 (en) | 2013-03-15 | 2016-01-20 | Lumena Pharmaceuticals, Inc. | Bile acid recycling inhibitors for treatment of barrett's esophagus and gastroesophageal reflux disease |
| WO2014144650A2 (en) | 2013-03-15 | 2014-09-18 | Lumena Pharmaceuticals, Inc. | Bile acid recycling inhibitors for treatment of primary sclerosing cholangitis and inflammatory bowel disease |
| BR112021015815A2 (pt) | 2019-02-12 | 2022-01-18 | Mirum Pharmaceuticals Inc | Métodos para tratar colestase |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0372422A (ja) * | 1989-05-16 | 1991-03-27 | Tanabe Seiyaku Co Ltd | 抗脂血剤 |
| JPH03157351A (ja) * | 1989-11-13 | 1991-07-05 | Tanabe Seiyaku Co Ltd | ナフタレン誘導体及びその製法 |
| DK0597107T3 (da) * | 1991-10-17 | 1996-07-29 | Shionogi & Co | Lignananalog, fremstilling deraf og hypolipidæmisk medikament |
-
1994
- 1994-04-12 EP EP94912092A patent/EP0646570B1/en not_active Expired - Lifetime
- 1994-04-12 AT AT94912092T patent/ATE167662T1/de not_active IP Right Cessation
- 1994-04-12 CA CA002138264A patent/CA2138264C/en not_active Expired - Fee Related
- 1994-04-12 US US08/356,199 patent/US5488134A/en not_active Expired - Fee Related
- 1994-04-12 ES ES94912092T patent/ES2119190T3/es not_active Expired - Lifetime
- 1994-04-12 CN CN94190286A patent/CN1046937C/zh not_active Expired - Fee Related
- 1994-04-12 KR KR1019940704565A patent/KR100277242B1/ko not_active Expired - Fee Related
- 1994-04-12 WO PCT/JP1994/000612 patent/WO1994024087A1/ja not_active Ceased
- 1994-04-12 DK DK94912092T patent/DK0646570T3/da active
- 1994-04-12 DE DE69411243T patent/DE69411243T2/de not_active Expired - Fee Related
- 1994-04-12 JP JP52298294A patent/JP3411036B2/ja not_active Expired - Fee Related
- 1994-04-12 AU AU64379/94A patent/AU666819B2/en not_active Ceased
- 1994-04-18 TW TW083103432A patent/TW255886B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP0646570A4 (en) | 1995-08-09 |
| JP3411036B2 (ja) | 2003-05-26 |
| ATE167662T1 (de) | 1998-07-15 |
| DK0646570T3 (da) | 1998-10-26 |
| DE69411243D1 (de) | 1998-07-30 |
| AU666819B2 (en) | 1996-02-22 |
| CN1046937C (zh) | 1999-12-01 |
| KR950701902A (ko) | 1995-05-17 |
| US5488134A (en) | 1996-01-30 |
| TW255886B (cg-RX-API-DMAC10.html) | 1995-09-01 |
| WO1994024087A1 (fr) | 1994-10-27 |
| CN1109685A (zh) | 1995-10-04 |
| DE69411243T2 (de) | 1998-11-19 |
| EP0646570A1 (en) | 1995-04-05 |
| AU6437994A (en) | 1994-11-08 |
| CA2138264A1 (en) | 1994-10-27 |
| EP0646570B1 (en) | 1998-06-24 |
| KR100277242B1 (ko) | 2001-02-01 |
| ES2119190T3 (es) | 1998-10-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2138264C (en) | Preparation of compounds of lignan series | |
| JP2559723B2 (ja) | ビニルフェノール誘導体 | |
| CA1069523A (en) | Process for preparing hypolipidaemiant products | |
| US4035376A (en) | Aroyl-substituted phenylacetic acid derivatives | |
| CZ209495A3 (en) | Synthesis process of (4r-cis)-1,1-dimethylethyl-6-cyanomethyl-2-2-dimethyl-1,3-dioxan-4-acetate and intermediates for such process | |
| JPWO1994024087A1 (ja) | リグナン系化合物の製造方法 | |
| AU724665B2 (en) | Synthesis of terfenadine and derivatives | |
| US4060528A (en) | Aroyl-substituted phenylmalonic acid derivatives | |
| US5089654A (en) | Chalcone derivatives | |
| US5599952A (en) | Methods of producing carboxylic acid ester derivatives and intermediates for use in the methods | |
| US4153719A (en) | Aromatic diketones | |
| JP4881298B2 (ja) | インデノールエステルまたはエーテルの製造方法 | |
| US4042617A (en) | Process for preparing a 2-methyl-(substituted aryl)-pyruvic acid compound | |
| US4064132A (en) | Aroyl-substituted phenylacetamide derivatives | |
| JPS584699B2 (ja) | 置換フエニル酢酸誘導体及びその製法 | |
| US4414391A (en) | A process for preparing 2-pyridinyloxyphenoxy-lower-alkanoates | |
| JP2549997B2 (ja) | 新規ハロケタール化合物 | |
| CA2121060C (en) | Preparation of lignan analogues | |
| US4891433A (en) | Process for the preparation of dibenzothiepin derivative | |
| US4410716A (en) | Dibenzo[a,d]cycloheptene derivatives and process for production thereof | |
| GB1574583A (en) | Process for preparing thiazoles | |
| JP2801647B2 (ja) | ６―フルオロクロモン―２―カルボン酸誘導体の製造法 | |
| CA1072110A (en) | Process for preparing hypolipidaemiant products | |
| KR20000075700A (ko) | 4ｈ-4-옥소-퀴놀리진-3-카복실산 유도체의 제조방법 | |
| JP3467072B2 (ja) | リグナン類縁体の製法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |