NO327749B1 - Oksy-substituerte isoflavan-4-ol og isoflav-3-en-forbindelser samt fremgangsmater for fremstilling av de samme - Google Patents
Oksy-substituerte isoflavan-4-ol og isoflav-3-en-forbindelser samt fremgangsmater for fremstilling av de samme Download PDFInfo
- Publication number
- NO327749B1 NO327749B1 NO20013945A NO20013945A NO327749B1 NO 327749 B1 NO327749 B1 NO 327749B1 NO 20013945 A NO20013945 A NO 20013945A NO 20013945 A NO20013945 A NO 20013945A NO 327749 B1 NO327749 B1 NO 327749B1
- Authority
- NO
- Norway
- Prior art keywords
- ene
- hydroxy
- compound
- arh
- diacetoxy
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 47
- KKBIDVILXNDFLH-UHFFFAOYSA-N 3-phenyl-3,4-dihydro-2h-chromen-4-ol Chemical class C1OC2=CC=CC=C2C(O)C1C1=CC=CC=C1 KKBIDVILXNDFLH-UHFFFAOYSA-N 0.000 title claims description 23
- CNNBJLXLTIKXGJ-UHFFFAOYSA-N 3-phenyl-2h-chromene Chemical class C1OC2=CC=CC=C2C=C1C1=CC=CC=C1 CNNBJLXLTIKXGJ-UHFFFAOYSA-N 0.000 title description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 90
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 80
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 54
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 51
- 239000001257 hydrogen Substances 0.000 claims description 49
- 229910052739 hydrogen Inorganic materials 0.000 claims description 49
- -1 isoflavone compound Chemical class 0.000 claims description 46
- 238000005984 hydrogenation reaction Methods 0.000 claims description 32
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 239000003054 catalyst Substances 0.000 claims description 28
- 150000002431 hydrogen Chemical class 0.000 claims description 27
- CJWQYWQDLBZGPD-UHFFFAOYSA-N isoflavone Natural products C1=C(OC)C(OC)=CC(OC)=C1C1=COC2=C(C=CC(C)(C)O3)C3=C(OC)C=C2C1=O CJWQYWQDLBZGPD-UHFFFAOYSA-N 0.000 claims description 27
- 235000008696 isoflavones Nutrition 0.000 claims description 27
- VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 claims description 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 22
- 125000003118 aryl group Chemical group 0.000 claims description 22
- 230000009467 reduction Effects 0.000 claims description 22
- ZZUBHVMHNVYXRR-UHFFFAOYSA-N 3-(4-hydroxyphenyl)-2h-chromen-7-ol Chemical compound C1=CC(O)=CC=C1C1=CC2=CC=C(O)C=C2OC1 ZZUBHVMHNVYXRR-UHFFFAOYSA-N 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 20
- 239000002904 solvent Substances 0.000 claims description 19
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 16
- 229910052763 palladium Inorganic materials 0.000 claims description 15
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 claims description 14
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims description 14
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 13
- 125000004414 alkyl thio group Chemical group 0.000 claims description 11
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 11
- 125000001188 haloalkyl group Chemical group 0.000 claims description 10
- 238000006297 dehydration reaction Methods 0.000 claims description 9
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 8
- 230000018044 dehydration Effects 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 8
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 8
- 125000006239 protecting group Chemical group 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
- PPYFYRMMSWPNRA-UHFFFAOYSA-N [4-hydroxy-3-(4-methoxyphenyl)-3,4-dihydro-2h-chromen-7-yl] acetate Chemical compound C1=CC(OC)=CC=C1C1C(O)C2=CC=C(OC(C)=O)C=C2OC1 PPYFYRMMSWPNRA-UHFFFAOYSA-N 0.000 claims description 7
- OHNFJXYAMHMPFN-UHFFFAOYSA-N [3-(4-methoxyphenyl)-2h-chromen-7-yl] acetate Chemical compound C1=CC(OC)=CC=C1C1=CC2=CC=C(OC(C)=O)C=C2OC1 OHNFJXYAMHMPFN-UHFFFAOYSA-N 0.000 claims description 5
- YMSTXUZPCGRBHY-UHFFFAOYSA-N [4-(7-acetyloxy-2h-chromen-3-yl)phenyl] acetate Chemical compound C1=CC(OC(=O)C)=CC=C1C1=CC2=CC=C(OC(C)=O)C=C2OC1 YMSTXUZPCGRBHY-UHFFFAOYSA-N 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 4
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 4
- 230000007062 hydrolysis Effects 0.000 claims description 4
- 238000006460 hydrolysis reaction Methods 0.000 claims description 4
- 235000002324 isoflavanes Nutrition 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- HFTUISPYTKQXKN-UHFFFAOYSA-N 3-(3-hydroxyphenyl)-2h-chromen-7-ol Chemical compound OC1=CC=CC(C=2COC3=CC(O)=CC=C3C=2)=C1 HFTUISPYTKQXKN-UHFFFAOYSA-N 0.000 claims description 3
- NPVLEUOTKFGWNV-UHFFFAOYSA-N 3-(3-methoxyphenyl)-2h-chromen-7-ol Chemical compound COC1=CC=CC(C=2COC3=CC(O)=CC=C3C=2)=C1 NPVLEUOTKFGWNV-UHFFFAOYSA-N 0.000 claims description 3
- KFBISZZPVNKBMC-UHFFFAOYSA-N 3-(4-hydroxy-3-methoxyphenyl)-8-methyl-2h-chromen-7-ol Chemical compound C1=C(O)C(OC)=CC(C=2COC3=C(C)C(O)=CC=C3C=2)=C1 KFBISZZPVNKBMC-UHFFFAOYSA-N 0.000 claims description 3
- DNYPQVFQEQIQQK-UHFFFAOYSA-N [4-(7-acetyloxy-4-hydroxy-3,4-dihydro-2h-chromen-3-yl)phenyl] acetate Chemical compound C1=CC(OC(=O)C)=CC=C1C1C(O)C2=CC=C(OC(C)=O)C=C2OC1 DNYPQVFQEQIQQK-UHFFFAOYSA-N 0.000 claims description 3
- ISLUWCQSNPONMM-UHFFFAOYSA-N [4-hydroxy-3-(3-methoxyphenyl)-3,4-dihydro-2h-chromen-7-yl] acetate Chemical compound COC1=CC=CC(C2C(C3=CC=C(OC(C)=O)C=C3OC2)O)=C1 ISLUWCQSNPONMM-UHFFFAOYSA-N 0.000 claims description 3
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 3
- 238000011031 large-scale manufacturing process Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims 7
- BEHFIWGOMWQJQZ-UHFFFAOYSA-N 2',7-dihydroxy-4',8-dimethoxyisoflavan-3 -ene Natural products OC1=CC(OC)=CC=C1C1=CC2=CC=C(O)C(OC)=C2OC1 BEHFIWGOMWQJQZ-UHFFFAOYSA-N 0.000 claims 2
- OATPBXKQXZVNBR-UHFFFAOYSA-N [3-(3-acetyloxyphenyl)-4-hydroxy-3,4-dihydro-2h-chromen-7-yl] acetate Chemical compound CC(=O)OC1=CC=CC(C2C(C3=CC=C(OC(C)=O)C=C3OC2)O)=C1 OATPBXKQXZVNBR-UHFFFAOYSA-N 0.000 claims 2
- MXSBGPUCTKSXHL-UHFFFAOYSA-N 3-(4-hydroxyphenyl)-2h-chromene-5,7-diol Chemical compound C1=CC(O)=CC=C1C1=CC2=C(O)C=C(O)C=C2OC1 MXSBGPUCTKSXHL-UHFFFAOYSA-N 0.000 claims 1
- KGETYGCVAMBRKY-UHFFFAOYSA-N C(C)(=O)OC1=CC=C2C(C(=COC2=C1)C1=CC(=CC=C1)OC)=O.C(C)(=O)OC=1C=C(C2=COC3=CC(=CC=C3C2=O)OC(C)=O)C=CC1.C(C)(=O)OC1=C(C=C(C2=COC3=C(C(=CC=C3C2=O)OC(C)=O)C)C=C1)OC Chemical compound C(C)(=O)OC1=CC=C2C(C(=COC2=C1)C1=CC(=CC=C1)OC)=O.C(C)(=O)OC=1C=C(C2=COC3=CC(=CC=C3C2=O)OC(C)=O)C=CC1.C(C)(=O)OC1=C(C=C(C2=COC3=C(C(=CC=C3C2=O)OC(C)=O)C)C=C1)OC KGETYGCVAMBRKY-UHFFFAOYSA-N 0.000 claims 1
- HGZRJEJLEPHEAS-UHFFFAOYSA-N C(C)(=O)OC1=CC=C2C(C(COC2=C1C)C1=CC=C(C=C1)OC)O.C(C)(=O)OC=1C=C(C2COC3=C(C(=CC=C3C2O)OC(C)=O)C)C=CC1.C(C)(=O)OC1=CC=C(C2COC3=C(C(=CC=C3C2O)OC(C)=O)C)C=C1.C(C)(=O)OC1=CC=C2C(C(COC2=C1OC(C)=O)C1=CC=C(C=C1)OC)O.C(C)(=O)OC1=CC=C(C2COC3=C(C(=CC=C3C2O)OC(C)=O)OC(C)=O)C=C1 Chemical compound C(C)(=O)OC1=CC=C2C(C(COC2=C1C)C1=CC=C(C=C1)OC)O.C(C)(=O)OC=1C=C(C2COC3=C(C(=CC=C3C2O)OC(C)=O)C)C=CC1.C(C)(=O)OC1=CC=C(C2COC3=C(C(=CC=C3C2O)OC(C)=O)C)C=C1.C(C)(=O)OC1=CC=C2C(C(COC2=C1OC(C)=O)C1=CC=C(C=C1)OC)O.C(C)(=O)OC1=CC=C(C2COC3=C(C(=CC=C3C2O)OC(C)=O)OC(C)=O)C=C1 HGZRJEJLEPHEAS-UHFFFAOYSA-N 0.000 claims 1
- KOVYHNGDYPOWAK-UHFFFAOYSA-N C(C)(=O)OC1=CC=C2C=C(COC2=C1C)C1=CC=C(C=C1)OC.C(C)(=O)OC=1C=C(C=2COC3=C(C(=CC=C3C2)OC(C)=O)C)C=CC1.C(C)(=O)OC1=CC=C(C=2COC3=C(C(=CC=C3C2)OC(C)=O)C)C=C1.C(C)(=O)OC1=CC=C2C=C(COC2=C1OC(C)=O)C1=CC=C(C=C1)OC.C(C)(=O)OC1=CC=C(C=2COC3=C(C(=CC=C3C2)OC(C)=O)OC(C)=O)C=C1 Chemical compound C(C)(=O)OC1=CC=C2C=C(COC2=C1C)C1=CC=C(C=C1)OC.C(C)(=O)OC=1C=C(C=2COC3=C(C(=CC=C3C2)OC(C)=O)C)C=CC1.C(C)(=O)OC1=CC=C(C=2COC3=C(C(=CC=C3C2)OC(C)=O)C)C=C1.C(C)(=O)OC1=CC=C2C=C(COC2=C1OC(C)=O)C1=CC=C(C=C1)OC.C(C)(=O)OC1=CC=C(C=2COC3=C(C(=CC=C3C2)OC(C)=O)OC(C)=O)C=C1 KOVYHNGDYPOWAK-UHFFFAOYSA-N 0.000 claims 1
- WAVIJKRMUZXEQQ-UHFFFAOYSA-N COC1=CC=C(C=2COC3=C(C(=CC=C3C2)O)C)C=C1.CC=1C(=CC=C2C=C(COC12)C1=CC(=CC=C1)O)O.CC=1C(=CC=C2C=C(COC12)C1=CC=C(C=C1)O)O.COC1=CC=C(C=2COC3=C(C(=CC=C3C2)O)O)C=C1.O1CC(=CC2=CC=C(C(=C12)O)O)C1=CC=C(C=C1)O Chemical compound COC1=CC=C(C=2COC3=C(C(=CC=C3C2)O)C)C=C1.CC=1C(=CC=C2C=C(COC12)C1=CC(=CC=C1)O)O.CC=1C(=CC=C2C=C(COC12)C1=CC=C(C=C1)O)O.COC1=CC=C(C=2COC3=C(C(=CC=C3C2)O)O)C=C1.O1CC(=CC2=CC=C(C(=C12)O)O)C1=CC=C(C=C1)O WAVIJKRMUZXEQQ-UHFFFAOYSA-N 0.000 claims 1
- XKVVYJAXUQERHL-UHFFFAOYSA-N COC=1C=C(C=2COC3=CC(=CC=C3C2)O)C=CC1.O1CC(=CC2=CC=C(C=C12)O)C1=CC(=CC=C1)O Chemical compound COC=1C=C(C=2COC3=CC(=CC=C3C2)O)C=CC1.O1CC(=CC2=CC=C(C=C12)O)C1=CC(=CC=C1)O XKVVYJAXUQERHL-UHFFFAOYSA-N 0.000 claims 1
- QCMOMSZNZSLUIH-UHFFFAOYSA-N OC1=CC=C2C(C(COC2=C1C)C1=CC=C(C=C1)OC)O.OC=1C=C(C2COC3=C(C(=CC=C3C2O)O)C)C=CC1.OC1=CC=C(C2COC3=C(C(=CC=C3C2O)O)C)C=C1.OC1=CC=C2C(C(COC2=C1O)C1=CC=C(C=C1)OC)O Chemical compound OC1=CC=C2C(C(COC2=C1C)C1=CC=C(C=C1)OC)O.OC=1C=C(C2COC3=C(C(=CC=C3C2O)O)C)C=CC1.OC1=CC=C(C2COC3=C(C(=CC=C3C2O)O)C)C=C1.OC1=CC=C2C(C(COC2=C1O)C1=CC=C(C=C1)OC)O QCMOMSZNZSLUIH-UHFFFAOYSA-N 0.000 claims 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 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 69
- 239000000203 mixture Substances 0.000 description 67
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 63
- 238000005481 NMR spectroscopy Methods 0.000 description 54
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 39
- 239000000047 product Substances 0.000 description 30
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 27
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 26
- 239000000243 solution Substances 0.000 description 24
- 150000002515 isoflavone derivatives Chemical class 0.000 description 22
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 21
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 19
- 238000006722 reduction reaction Methods 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 238000001819 mass spectrum Methods 0.000 description 17
- 239000000725 suspension Substances 0.000 description 16
- 239000000706 filtrate Substances 0.000 description 14
- 238000005160 1H NMR spectroscopy Methods 0.000 description 13
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000001914 filtration Methods 0.000 description 11
- 229910052786 argon Inorganic materials 0.000 description 10
- 125000005843 halogen group Chemical group 0.000 description 9
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 8
- GGGJVAAAUYBGSQ-UHFFFAOYSA-N [3-(4-methoxyphenyl)-4-oxochromen-7-yl] acetate Chemical compound C1=CC(OC)=CC=C1C1=COC2=CC(OC(C)=O)=CC=C2C1=O GGGJVAAAUYBGSQ-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000012153 distilled water Substances 0.000 description 8
- XXFWTQQLVJUOAD-UHFFFAOYSA-N [4-(7-acetyloxy-8-methyl-4-oxochromen-3-yl)phenyl] acetate Chemical compound C1=CC(OC(=O)C)=CC=C1C1=COC2=C(C)C(OC(C)=O)=CC=C2C1=O XXFWTQQLVJUOAD-UHFFFAOYSA-N 0.000 description 7
- CSCPPACGZOOCGX-WFGJKAKNSA-N acetone d6 Chemical compound [2H]C([2H])([2H])C(=O)C([2H])([2H])[2H] CSCPPACGZOOCGX-WFGJKAKNSA-N 0.000 description 6
- YKIOKAURTKXMSB-UHFFFAOYSA-N adams's catalyst Chemical compound O=[Pt]=O YKIOKAURTKXMSB-UHFFFAOYSA-N 0.000 description 6
- ZQSIJRDFPHDXIC-UHFFFAOYSA-N daidzein Chemical compound C1=CC(O)=CC=C1C1=COC2=CC(O)=CC=C2C1=O ZQSIJRDFPHDXIC-UHFFFAOYSA-N 0.000 description 6
- ADFCQWZHKCXPAJ-GFCCVEGCSA-N equol Chemical compound C1=CC(O)=CC=C1[C@@H]1CC2=CC=C(O)C=C2OC1 ADFCQWZHKCXPAJ-GFCCVEGCSA-N 0.000 description 6
- ADFCQWZHKCXPAJ-UHFFFAOYSA-N indofine Natural products C1=CC(O)=CC=C1C1CC2=CC=C(O)C=C2OC1 ADFCQWZHKCXPAJ-UHFFFAOYSA-N 0.000 description 6
- NNQSGBRGJHSRFN-UHFFFAOYSA-N isoflavan Chemical class C1OC2=CC=CC=C2CC1C1=CC=CC=C1 NNQSGBRGJHSRFN-UHFFFAOYSA-N 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- ADLILDQUGSRCIY-UHFFFAOYSA-N 3-(4-hydroxyphenyl)-8-methyl-2h-chromen-7-ol Chemical compound C1OC=2C(C)=C(O)C=CC=2C=C1C1=CC=C(O)C=C1 ADLILDQUGSRCIY-UHFFFAOYSA-N 0.000 description 5
- DGBHTUVYXZHRNQ-UHFFFAOYSA-N [4-(7,8-diacetyloxy-4-oxochromen-3-yl)phenyl] acetate Chemical compound C1=CC(OC(=O)C)=CC=C1C1=COC2=C(OC(C)=O)C(OC(C)=O)=CC=C2C1=O DGBHTUVYXZHRNQ-UHFFFAOYSA-N 0.000 description 5
- 239000012043 crude product Substances 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- 239000000741 silica gel Substances 0.000 description 5
- 229910002027 silica gel Inorganic materials 0.000 description 5
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 4
- DLXIJJURUIXRFK-UHFFFAOYSA-N 7,8-dihydroxy-3-(4-methoxyphenyl)chromen-4-one Chemical compound C1=CC(OC)=CC=C1C1=COC2=C(O)C(O)=CC=C2C1=O DLXIJJURUIXRFK-UHFFFAOYSA-N 0.000 description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
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- YOSDNAMJVOLJKI-DZGCQCFKSA-N (3r,4s)-3-(4-hydroxyphenyl)-3,4-dihydro-2h-chromene-4,7-diol Chemical compound C1([C@H]2[C@@H](C3=CC=C(O)C=C3OC2)O)=CC=C(O)C=C1 YOSDNAMJVOLJKI-DZGCQCFKSA-N 0.000 description 1
- KKBIDVILXNDFLH-DZGCQCFKSA-N (3r,4s)-3-phenyl-3,4-dihydro-2h-chromen-4-ol Chemical compound C1([C@H]2[C@@H](C3=CC=CC=C3OC2)O)=CC=CC=C1 KKBIDVILXNDFLH-DZGCQCFKSA-N 0.000 description 1
- QJRXKXPIKSHLOO-DZGCQCFKSA-N (3r,4s)-3-phenyl-3,4-dihydro-2h-chromene-4,7-diol Chemical compound C1([C@H]2[C@@H](C3=CC=C(O)C=C3OC2)O)=CC=CC=C1 QJRXKXPIKSHLOO-DZGCQCFKSA-N 0.000 description 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- QQNSLDJJYHEKKA-UHFFFAOYSA-N 3-(3-hydroxyphenyl)-8-methyl-3,4-dihydro-2h-chromene-4,7-diol Chemical compound C1OC=2C(C)=C(O)C=CC=2C(O)C1C1=CC=CC(O)=C1 QQNSLDJJYHEKKA-UHFFFAOYSA-N 0.000 description 1
- OAMVVDBAFXQCKD-UHFFFAOYSA-N 3-(4-hydroxy-3-methoxyphenyl)-2h-chromen-7-ol Chemical compound C1=C(O)C(OC)=CC(C=2COC3=CC(O)=CC=C3C=2)=C1 OAMVVDBAFXQCKD-UHFFFAOYSA-N 0.000 description 1
- BNTLMCIMLNLCPE-UHFFFAOYSA-N 3-(4-hydroxyphenyl)-3,4-dihydro-2h-chromene-4,7,8-triol Chemical compound C1OC2=C(O)C(O)=CC=C2C(O)C1C1=CC=C(O)C=C1 BNTLMCIMLNLCPE-UHFFFAOYSA-N 0.000 description 1
- NNRYVLYFAISUDT-UHFFFAOYSA-N 3-(4-methoxyphenyl)-8-methyl-3,4-dihydro-2h-chromene-4,7-diol Chemical compound C1=CC(OC)=CC=C1C1C(O)C2=CC=C(O)C(C)=C2OC1 NNRYVLYFAISUDT-UHFFFAOYSA-N 0.000 description 1
- ZHPXMPOMTOUGJL-UHFFFAOYSA-N 3-phenyl-3,4,4a,5,6,7-hexahydro-2h-chromen-4-ol Chemical compound OC1C2CCCC=C2OCC1C1=CC=CC=C1 ZHPXMPOMTOUGJL-UHFFFAOYSA-N 0.000 description 1
- QJRXKXPIKSHLOO-UHFFFAOYSA-N 3-phenyl-3,4-dihydro-2h-chromene-4,7-diol Chemical compound C1OC2=CC(O)=CC=C2C(O)C1C1=CC=CC=C1 QJRXKXPIKSHLOO-UHFFFAOYSA-N 0.000 description 1
- HUQBHTLDXGAPPG-UHFFFAOYSA-N 3-phenyl-4h-chromene Chemical class C=1OC2=CC=CC=C2CC=1C1=CC=CC=C1 HUQBHTLDXGAPPG-UHFFFAOYSA-N 0.000 description 1
- IKRPUQYROLWULZ-UHFFFAOYSA-N 7-hydroxy-3-(3-hydroxyphenyl)-8-methylchromen-4-one Chemical compound CC1=C(O)C=CC(C2=O)=C1OC=C2C1=CC=CC(O)=C1 IKRPUQYROLWULZ-UHFFFAOYSA-N 0.000 description 1
- RDYQZFNYNCDTFW-UHFFFAOYSA-N 7-hydroxy-3-(3-hydroxyphenyl)chromen-4-one Chemical compound OC1=CC=CC(C=2C(C3=CC=C(O)C=C3OC=2)=O)=C1 RDYQZFNYNCDTFW-UHFFFAOYSA-N 0.000 description 1
- SVIVXHGAPCFWCS-UHFFFAOYSA-N 7-hydroxy-3-(3-methoxyphenyl)chromen-4-one Chemical compound COC1=CC=CC(C=2C(C3=CC=C(O)C=C3OC=2)=O)=C1 SVIVXHGAPCFWCS-UHFFFAOYSA-N 0.000 description 1
- CNPDHUJKSWUXEK-UHFFFAOYSA-N 7-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-8-methylchromen-4-one Chemical compound C1=C(O)C(OC)=CC(C=2C(C3=CC=C(O)C(C)=C3OC=2)=O)=C1 CNPDHUJKSWUXEK-UHFFFAOYSA-N 0.000 description 1
- WSWZVNSJDDRIHL-UHFFFAOYSA-N 7-hydroxy-3-(4-hydroxyphenyl)-8-methylchromen-4-one Chemical compound CC1=C(O)C=CC(C2=O)=C1OC=C2C1=CC=C(O)C=C1 WSWZVNSJDDRIHL-UHFFFAOYSA-N 0.000 description 1
- XEKNYFGOJLESFJ-UHFFFAOYSA-N 7-hydroxy-3-(4-methoxyphenyl)-8-methyl-2,3-dihydrochromen-4-one Chemical compound C1=CC(OC)=CC=C1C1C(=O)C2=CC=C(O)C(C)=C2OC1 XEKNYFGOJLESFJ-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 1
- INYISIYHXQDCPK-UHFFFAOYSA-N Dihydroformononetin Chemical compound C1=CC(OC)=CC=C1C1C(=O)C2=CC=C(O)C=C2OC1 INYISIYHXQDCPK-UHFFFAOYSA-N 0.000 description 1
- INYISIYHXQDCPK-CQSZACIVSA-N Dihydroformononetin Natural products C1=CC(OC)=CC=C1[C@@H]1C(=O)C2=CC=C(O)C=C2OC1 INYISIYHXQDCPK-CQSZACIVSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 240000004322 Lens culinaris Species 0.000 description 1
- 235000014647 Lens culinaris subsp culinaris Nutrition 0.000 description 1
- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
- 206010067572 Oestrogenic effect Diseases 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 231100000766 Possible carcinogen Toxicity 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- OATPBXKQXZVNBR-PKOBYXMFSA-N [(3r,4s)-3-(3-acetyloxyphenyl)-4-hydroxy-3,4-dihydro-2h-chromen-7-yl] acetate Chemical compound CC(=O)OC1=CC=CC([C@H]2[C@@H](C3=CC=C(OC(C)=O)C=C3OC2)O)=C1 OATPBXKQXZVNBR-PKOBYXMFSA-N 0.000 description 1
- JEONSOMPTGOTQS-UHFFFAOYSA-N [3-(3-acetyloxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl] acetate Chemical compound CC(=O)OC1=CC=CC(C2C(C3=CC=C(OC(C)=O)C=C3OC2)=O)=C1 JEONSOMPTGOTQS-UHFFFAOYSA-N 0.000 description 1
- TUEZBRGVWIMWTO-UHFFFAOYSA-N [3-(3-acetyloxyphenyl)-4-oxochromen-7-yl] acetate Chemical compound CC(=O)OC1=CC=CC(C=2C(C3=CC=C(OC(C)=O)C=C3OC=2)=O)=C1 TUEZBRGVWIMWTO-UHFFFAOYSA-N 0.000 description 1
- PWGZLQCRLSPFLS-UHFFFAOYSA-N [3-(4-acetyloxy-3-methoxyphenyl)-4-hydroxy-3,4-dihydro-2h-chromen-7-yl] acetate Chemical compound C1=C(OC(C)=O)C(OC)=CC(C2C(C3=CC=C(OC(C)=O)C=C3OC2)O)=C1 PWGZLQCRLSPFLS-UHFFFAOYSA-N 0.000 description 1
- YJCQZPBEAPAFLS-UHFFFAOYSA-N [3-(4-acetyloxy-3-methoxyphenyl)-8-methyl-4-oxochromen-7-yl] acetate;[4-(5,7-diacetyloxy-4-oxochromen-3-yl)phenyl] acetate Chemical compound C1=C(OC(C)=O)C(OC)=CC(C=2C(C3=CC=C(OC(C)=O)C(C)=C3OC=2)=O)=C1.C1=CC(OC(=O)C)=CC=C1C1=COC2=CC(OC(C)=O)=CC(OC(C)=O)=C2C1=O YJCQZPBEAPAFLS-UHFFFAOYSA-N 0.000 description 1
- FZMVBBSMLVGUHM-UHFFFAOYSA-N [4-(7-acetyloxy-3,4-dihydro-2h-chromen-3-yl)phenyl] acetate Chemical compound C1=CC(OC(=O)C)=CC=C1C1CC2=CC=C(OC(C)=O)C=C2OC1 FZMVBBSMLVGUHM-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 238000006640 acetylation reaction Methods 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- CODNYICXDISAEA-UHFFFAOYSA-N bromine monochloride Chemical compound BrCl CODNYICXDISAEA-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000011210 chromatographic step Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000001076 estrogenic effect Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 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
- 229930012930 isoflavone derivative Natural products 0.000 description 1
- 229930013032 isoflavonoid Natural products 0.000 description 1
- 150000003817 isoflavonoid derivatives Chemical class 0.000 description 1
- 235000012891 isoflavonoids Nutrition 0.000 description 1
- 238000010667 large scale reaction Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- NXJCBFBQEVOTOW-UHFFFAOYSA-L palladium(2+);dihydroxide Chemical compound O[Pd]O NXJCBFBQEVOTOW-UHFFFAOYSA-L 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 150000003283 rhodium Chemical class 0.000 description 1
- QBERHIJABFXGRZ-UHFFFAOYSA-M rhodium;triphenylphosphane;chloride Chemical compound [Cl-].[Rh].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 QBERHIJABFXGRZ-UHFFFAOYSA-M 0.000 description 1
- 150000003303 ruthenium Chemical class 0.000 description 1
- JDNQPKBFOBQRBN-UHFFFAOYSA-N ruthenium monohydride Chemical compound [RuH] JDNQPKBFOBQRBN-UHFFFAOYSA-N 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
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/42—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4
- C07D311/56—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms in positions 2 and 4 without hydrogen atoms in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/22—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
- C07D311/26—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3
- C07D311/34—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3 with aromatic rings attached in position 3 only
- C07D311/36—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3 with aromatic rings attached in position 3 only not hydrogenated in the hetero ring, e.g. isoflavones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/22—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
- C07D311/26—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3
- C07D311/34—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3 with aromatic rings attached in position 3 only
- C07D311/38—2,3-Dihydro derivatives, e.g. isoflavanones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrane Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPP8685A AUPP868599A0 (en) | 1999-02-15 | 1999-02-15 | Production of isoflavone derivatives |
| PCT/AU2000/000103 WO2000049009A1 (fr) | 1999-02-15 | 2000-02-15 | Derives d'isoflavone |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20013945D0 NO20013945D0 (no) | 2001-08-14 |
| NO20013945L NO20013945L (no) | 2001-08-14 |
| NO327749B1 true NO327749B1 (no) | 2009-09-14 |
Family
ID=3812886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20013945A NO327749B1 (no) | 1999-02-15 | 2001-08-14 | Oksy-substituerte isoflavan-4-ol og isoflav-3-en-forbindelser samt fremgangsmater for fremstilling av de samme |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US20050143588A1 (fr) |
| EP (1) | EP1153020A4 (fr) |
| JP (1) | JP2002537295A (fr) |
| CN (1) | CN100564370C (fr) |
| AU (2) | AUPP868599A0 (fr) |
| BR (1) | BR0008222A (fr) |
| CA (1) | CA2362819C (fr) |
| CZ (1) | CZ20012920A3 (fr) |
| HK (1) | HK1041883B (fr) |
| HU (1) | HUP0105218A3 (fr) |
| IL (2) | IL144008A0 (fr) |
| NO (1) | NO327749B1 (fr) |
| NZ (1) | NZ538323A (fr) |
| TR (1) | TR200102367T2 (fr) |
| WO (1) | WO2000049009A1 (fr) |
| ZA (1) | ZA200106502B (fr) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU683838B2 (en) * | 1992-05-19 | 1997-11-27 | Novogen Research Pty Ltd | Health supplements containing phyto-oestrogens, analogues or metabolites thereof |
| NZ527735A (en) * | 1997-05-01 | 2005-10-28 | Novogen Inc | Treatment or prevention of menopausal symptoms and osteoporosis |
| AUPP260798A0 (en) * | 1998-03-26 | 1998-04-23 | Novogen Research Pty Ltd | Treatment of medical related conditions with isoflavone containing extracts of clover |
| US20040072765A1 (en) * | 1999-04-28 | 2004-04-15 | Novogen Research Pty Ltd. | Cardiovascular and bone treatment using isoflavones |
| AUPQ266199A0 (en) * | 1999-09-06 | 1999-09-30 | Novogen Research Pty Ltd | Compositions and therapeutic methods involving isoflavones and analogues thereof |
| AUPQ520300A0 (en) * | 2000-01-21 | 2000-02-17 | Novogen Research Pty Ltd | Food product and process |
| KR100436220B1 (ko) * | 2001-08-30 | 2004-06-12 | 주식회사 네패스 | 바닥 반사방지막용 유기 중합체, 그의 제조방법 및 그를함유하는 조성물 |
| JP2005528391A (ja) * | 2002-04-09 | 2005-09-22 | ノボゲン リサーチ ピーティーワイ リミテッド | イソフラブ−３−エン及びイソフラバン構造を含む治療方法及び組成物 |
| JP2006504409A (ja) * | 2002-07-24 | 2006-02-09 | チルドレンズ ホスピタル メディカル センター | 鏡像異性のエクオールを含有する組成物および製品、およびその製造方法 |
| US8668914B2 (en) | 2002-07-24 | 2014-03-11 | Brigham Young University | Use of equol for treating skin diseases |
| WO2004039327A2 (fr) | 2002-10-29 | 2004-05-13 | Colorado State University Research Foundation | Utilisation d'equol dans le traitement de maladies d'origine androgenique |
| AU2003255232A1 (en) | 2002-08-07 | 2004-02-25 | University Of Mississippi | Antigiardial agents and use thereof |
| AU2002951271A0 (en) * | 2002-09-06 | 2002-09-19 | Novogen Research Pty Ltd | Repair of dna mutagenic damage |
| AU2003257264B2 (en) * | 2002-09-06 | 2007-09-13 | Novogen Research Pty Ltd | Repair of DNA mutagenic damage |
| CA2499602A1 (fr) * | 2002-09-23 | 2004-04-01 | Graham Edmund Kelly | Traitement du photovieillissement et de la deterioration actinique de la peau |
| AU2002951833A0 (en) | 2002-10-02 | 2002-10-24 | Novogen Research Pty Ltd | Compositions and therapeutic methods invloving platinum complexes |
| US8580846B2 (en) | 2002-10-29 | 2013-11-12 | Brigham Young University | Use of equol for ameliorating or preventing neuropsychiatric and neurodegenerative diseases or disorders |
| CA2581316C (fr) | 2004-09-21 | 2013-09-10 | Novogen Research Pty Ltd | Derives de chromane substitues, medicaments et utilisation a des fins therapeutiques |
| EP1809618B1 (fr) | 2004-09-21 | 2013-07-17 | Marshall Edwards, Inc. | Dérivés de chromane, médicaments et utilisation à des fins thérapeutiques |
| US8080675B2 (en) | 2004-09-21 | 2011-12-20 | Marshall Edwards, Inc. | Chroman derivatives, medicaments and use in therapy |
| US7528267B2 (en) | 2005-08-01 | 2009-05-05 | Girindus America, Inc. | Method for enantioselective hydrogenation of chromenes |
| US7696363B2 (en) * | 2005-12-02 | 2010-04-13 | Yasoo Health Inc. | Preparation of flavonoid compounds |
| US20070203227A1 (en) * | 2006-02-24 | 2007-08-30 | Herman Adlercreutz | Isoflavan and isoflavene compounds and their use as angiogenesis inhibitors |
| EP2133080A1 (fr) | 2008-06-13 | 2009-12-16 | Haelan Schweiz GmbH | Compositions contenant de l'équol |
| US7875736B2 (en) | 2009-05-19 | 2011-01-25 | Kaohsiung Medical University | Intermediate compounds and processes for the preparation of 7-benzyloxy-3-(4-methoxyphenyl)-2H-1-benzopyran |
| US7875735B2 (en) | 2009-05-19 | 2011-01-25 | Kaohsiung Medical University | Processes for preparing isoflavonoids using 7-benzyloxy-3-(4-methoxyphenyl)-2H-1-benzopyran as a starting material |
| EP2635121B1 (fr) | 2010-11-01 | 2020-01-08 | MEI Pharma, Inc. | Composés d'isoflavonoïdes et procédés pour le traitement du cancer |
| US9279082B2 (en) * | 2011-01-20 | 2016-03-08 | Merck Patent Gmbh | Polymerisable compounds and the use thereof in liquid-crystal displays |
| WO2014145386A2 (fr) * | 2013-03-15 | 2014-09-18 | University Of Florida Research Foundation Incorporated | Nouveaux inhibiteurs allostériques de thymidylate synthase |
| JP2016522167A (ja) * | 2013-04-04 | 2016-07-28 | ジ アドミニストレーターズ オブ ザ トゥレーン エデュケーショナル ファンド | ヒト間葉系幹細胞に対するダイゼイン類似体の骨形成活性の向上 |
| CN103224481A (zh) * | 2013-05-20 | 2013-07-31 | 黑龙江大学 | 一种去氢雌马酚的制备方法 |
| CN107427003B (zh) | 2015-02-02 | 2023-01-31 | 梅制药公司 | 联合治疗 |
| WO2016209688A1 (fr) | 2015-06-24 | 2016-12-29 | University Of Florida Research Foundation, Incorporated | Compositions destinées au traitement du cancer, et leurs utilisations |
| CN107459554B (zh) * | 2016-06-03 | 2021-03-30 | 首都医科大学 | 4’,7-二氧乙酰-apak-5-羟基异黄酮,其合成,活性和应用 |
| CN111303106B (zh) * | 2020-03-23 | 2023-06-02 | 武汉轻工大学 | 一种5,6-二乙酰氧基-7-羟基黄酮的制备方法 |
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| DE1518002C3 (de) * | 1965-01-02 | 1975-01-23 | Merck Patent Gmbh, 6100 Darmstadt | Isoflavane und Isoflavene und Verfahren zu Ihrer Herstellung sowie diese enthaltende Arzneimittel |
| DE1543749A1 (de) * | 1966-02-16 | 1969-12-11 | Merck Ag E | Verfahren zur Herstellung von 3,4-cis-4-Aryl-isoflavanen |
| JPS5035393A (fr) * | 1973-08-01 | 1975-04-04 | ||
| JPS576427B2 (fr) * | 1974-01-25 | 1982-02-04 | ||
| JPS50160483A (fr) * | 1974-06-19 | 1975-12-25 | ||
| US4264509A (en) * | 1977-06-08 | 1981-04-28 | Z-L Limited Partnership | Isoflavones and related compounds, methods of preparing and using and antioxidant compositions containing same |
| US4366082A (en) * | 1979-04-11 | 1982-12-28 | Z-L Limited Partnership | Isoflavones and related compounds, methods of preparing and using and antioxidant compositions containing same |
| GB8626344D0 (en) * | 1986-11-04 | 1986-12-03 | Zyma Sa | Bicyclic compounds |
| JPH0832632B2 (ja) * | 1988-03-08 | 1996-03-29 | 株式会社太田胃散 | 尿素窒素代謝改善剤 |
| JPH02124883A (ja) * | 1988-11-04 | 1990-05-14 | Kitasato Inst:The | 抗酸化作用を有するイソフラボン誘導体およびその製造法 |
| JPH0686682A (ja) * | 1992-07-23 | 1994-03-29 | Kobe Steel Ltd | ４’，７，８−トリヒドロキシイソフラボンの製造方法 |
| JPH0640909A (ja) * | 1992-07-23 | 1994-02-15 | Kobe Steel Ltd | スーパーオキシド・ディスムターゼ様活性剤 |
| JPH0640876A (ja) * | 1992-07-23 | 1994-02-15 | Kobe Steel Ltd | 紫外線障害防御外用剤 |
| JPH06321752A (ja) * | 1993-05-07 | 1994-11-22 | Kao Corp | 美白剤 |
| HUT68558A (en) * | 1993-07-20 | 1995-06-28 | Chinoin Gyogyszer Es Vegyeszet | Method for preparing isoflavon derivatives |
| AU5970496A (en) * | 1995-06-07 | 1996-12-30 | Patrick C. Kung | Compounds and methods for promoting hair growth |
| JPH1059956A (ja) * | 1996-08-22 | 1998-03-03 | Kikkoman Corp | 新規イソフラボン誘導体及びその製造法 |
| AUPO203996A0 (en) * | 1996-08-30 | 1996-09-26 | Novogen Research Pty Ltd | Therapeutic uses |
| AUPP112497A0 (en) * | 1997-12-24 | 1998-01-22 | Novogen Research Pty Ltd | Compositions and method for protecting skin from UV induced immunosupression and skin damage |
| AU2183899A (en) * | 1998-01-27 | 1999-08-09 | Shionogi & Co., Ltd. | Isoflavane derivatives and immunopotentiating compositions containing the same |
-
1999
- 1999-02-15 AU AUPP8685A patent/AUPP868599A0/en not_active Abandoned
-
2000
- 2000-02-15 CA CA2362819A patent/CA2362819C/fr not_active Expired - Fee Related
- 2000-02-15 TR TR2001/02367T patent/TR200102367T2/xx unknown
- 2000-02-15 JP JP2000599749A patent/JP2002537295A/ja active Pending
- 2000-02-15 NZ NZ538323A patent/NZ538323A/en not_active IP Right Cessation
- 2000-02-15 HU HU0105218A patent/HUP0105218A3/hu unknown
- 2000-02-15 CZ CZ20012920A patent/CZ20012920A3/cs unknown
- 2000-02-15 AU AU26510/00A patent/AU2651000A/en not_active Abandoned
- 2000-02-15 WO PCT/AU2000/000103 patent/WO2000049009A1/fr active Application Filing
- 2000-02-15 EP EP00904727A patent/EP1153020A4/fr not_active Withdrawn
- 2000-02-15 CN CNB008038163A patent/CN100564370C/zh not_active Expired - Fee Related
- 2000-02-15 IL IL14400800A patent/IL144008A0/xx active IP Right Grant
- 2000-02-15 BR BR0008222-8A patent/BR0008222A/pt not_active Application Discontinuation
-
2001
- 2001-06-26 IL IL144008A patent/IL144008A/en not_active IP Right Cessation
- 2001-08-07 ZA ZA200106502A patent/ZA200106502B/en unknown
- 2001-08-14 NO NO20013945A patent/NO327749B1/no not_active IP Right Cessation
-
2002
- 2002-05-17 HK HK02103732.5A patent/HK1041883B/zh not_active IP Right Cessation
-
2004
- 2004-05-20 US US10/851,270 patent/US20050143588A1/en not_active Abandoned
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2006
- 2006-05-25 US US11/442,369 patent/US7906660B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| NZ538323A (en) | 2005-10-28 |
| AU2651000A (en) | 2000-09-04 |
| IL144008A (en) | 2011-03-31 |
| HK1041883A1 (en) | 2002-07-26 |
| CZ20012920A3 (cs) | 2001-11-14 |
| US20050143588A1 (en) | 2005-06-30 |
| CA2362819A1 (fr) | 2000-08-24 |
| TR200102367T2 (tr) | 2001-11-21 |
| AUPP868599A0 (en) | 1999-03-11 |
| CN100564370C (zh) | 2009-12-02 |
| HUP0105218A1 (hu) | 2002-07-29 |
| US20060217564A1 (en) | 2006-09-28 |
| IL144008A0 (en) | 2002-04-21 |
| EP1153020A1 (fr) | 2001-11-14 |
| HUP0105218A3 (en) | 2002-10-28 |
| US7906660B2 (en) | 2011-03-15 |
| HK1041883B (zh) | 2010-04-23 |
| CN1340048A (zh) | 2002-03-13 |
| ZA200106502B (en) | 2005-05-09 |
| NO20013945D0 (no) | 2001-08-14 |
| EP1153020A4 (fr) | 2002-08-21 |
| WO2000049009A1 (fr) | 2000-08-24 |
| NO20013945L (no) | 2001-08-14 |
| BR0008222A (pt) | 2001-10-30 |
| JP2002537295A (ja) | 2002-11-05 |
| CA2362819C (fr) | 2011-05-10 |
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