ZA200106502B - Production of isoflavone derivatives. - Google Patents
Production of isoflavone derivatives. Download PDFInfo
- Publication number
- ZA200106502B ZA200106502B ZA200106502A ZA200106502A ZA200106502B ZA 200106502 B ZA200106502 B ZA 200106502B ZA 200106502 A ZA200106502 A ZA 200106502A ZA 200106502 A ZA200106502 A ZA 200106502A ZA 200106502 B ZA200106502 B ZA 200106502B
- Authority
- ZA
- South Africa
- Prior art keywords
- ene
- compound
- hydroxy
- formula
- arh
- Prior art date
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- 150000002515 isoflavone derivatives Chemical class 0.000 title description 24
- 229930012930 isoflavone derivative Natural products 0.000 title description 3
- 238000004519 manufacturing process Methods 0.000 title description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 79
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 78
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 60
- 238000000034 method Methods 0.000 claims description 53
- 239000001257 hydrogen Substances 0.000 claims description 48
- 229910052739 hydrogen Inorganic materials 0.000 claims description 48
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 48
- -1 isoflavone compound Chemical class 0.000 claims description 44
- 238000005984 hydrogenation reaction Methods 0.000 claims description 37
- 150000001875 compounds Chemical class 0.000 claims description 36
- 239000003054 catalyst Substances 0.000 claims description 29
- 150000002431 hydrogen Chemical class 0.000 claims description 28
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- 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 26
- 235000008696 isoflavones Nutrition 0.000 claims description 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 25
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims description 24
- 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 22
- 230000009467 reduction Effects 0.000 claims description 22
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 20
- 125000003118 aryl group Chemical group 0.000 claims description 20
- 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 claims description 19
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 18
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 17
- 229910052763 palladium Inorganic materials 0.000 claims description 17
- 125000001188 haloalkyl group Chemical group 0.000 claims description 11
- 238000006297 dehydration reaction Methods 0.000 claims description 10
- 125000001424 substituent group Chemical group 0.000 claims description 10
- YKIOKAURTKXMSB-UHFFFAOYSA-N adams's catalyst Chemical compound O=[Pt]=O YKIOKAURTKXMSB-UHFFFAOYSA-N 0.000 claims description 9
- 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 9
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims 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 claims description 8
- 125000004414 alkyl thio group Chemical group 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
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 8
- 125000006239 protecting group Chemical group 0.000 claims description 7
- 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 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 6
- 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
- OHNNFNBOPWLDFH-UHFFFAOYSA-N [4-(7-acetyloxy-4-oxochromen-3-yl)phenyl] acetate Chemical compound C1=CC(OC(=O)C)=CC=C1C1=COC2=CC(OC(C)=O)=CC=C2C1=O OHNNFNBOPWLDFH-UHFFFAOYSA-N 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 5
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 5
- FGNQWCLJWZMGFQ-UHFFFAOYSA-N 3-(4-methoxyphenyl)-2h-chromen-7-ol Chemical compound C1=CC(OC)=CC=C1C1=CC2=CC=C(O)C=C2OC1 FGNQWCLJWZMGFQ-UHFFFAOYSA-N 0.000 claims description 4
- ZTHHHLXSEUUASE-UHFFFAOYSA-N [4-(7-acetyloxy-4-oxo-2,3-dihydrochromen-3-yl)phenyl] acetate Chemical group C1=CC(OC(=O)C)=CC=C1C1C(=O)C2=CC=C(OC(C)=O)C=C2OC1 ZTHHHLXSEUUASE-UHFFFAOYSA-N 0.000 claims description 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 4
- JHYXBPPMXZIHKG-UHFFFAOYSA-N dihydrodaidzein Chemical compound C1=CC(O)=CC=C1C1C(=O)C2=CC=C(O)C=C2OC1 JHYXBPPMXZIHKG-UHFFFAOYSA-N 0.000 claims description 4
- NXJCBFBQEVOTOW-UHFFFAOYSA-L palladium(2+);dihydroxide Chemical compound O[Pd]O NXJCBFBQEVOTOW-UHFFFAOYSA-L 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[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
- 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 2
- 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 description 2
- 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 2
- 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 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 3
- 125000001475 halogen functional group Chemical group 0.000 claims 3
- 230000007062 hydrolysis Effects 0.000 claims 3
- 238000006460 hydrolysis reaction Methods 0.000 claims 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 2
- 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
- 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 1
- WVGGTDYBXLAOPN-UHFFFAOYSA-N [8-acetyloxy-3-(4-methoxyphenyl)-2h-chromen-7-yl] acetate Chemical compound C1=CC(OC)=CC=C1C1=CC2=CC=C(OC(C)=O)C(OC(C)=O)=C2OC1 WVGGTDYBXLAOPN-UHFFFAOYSA-N 0.000 claims 1
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 claims 1
- 229910052702 rhenium Inorganic materials 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 69
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 65
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 63
- 238000005481 NMR spectroscopy Methods 0.000 description 55
- 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 33
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 26
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 26
- 239000000243 solution Substances 0.000 description 24
- 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
- 238000001819 mass spectrum Methods 0.000 description 17
- 238000006722 reduction reaction Methods 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 238000005160 1H NMR spectroscopy Methods 0.000 description 16
- 239000000725 suspension Substances 0.000 description 16
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N DMSO Substances CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 14
- 239000000706 filtrate Substances 0.000 description 14
- 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
- CNNBJLXLTIKXGJ-UHFFFAOYSA-N 3-phenyl-2h-chromene Chemical class C1OC2=CC=CC=C2C=C1C1=CC=CC=C1 CNNBJLXLTIKXGJ-UHFFFAOYSA-N 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000001914 filtration Methods 0.000 description 11
- 238000003786 synthesis reaction Methods 0.000 description 11
- 229910052786 argon Inorganic materials 0.000 description 10
- ZQSIJRDFPHDXIC-UHFFFAOYSA-N daidzein Chemical compound C1=CC(O)=CC=C1C1=COC2=CC(O)=CC=C2C1=O ZQSIJRDFPHDXIC-UHFFFAOYSA-N 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Substances CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000012153 distilled water Substances 0.000 description 8
- 125000005843 halogen group Chemical group 0.000 description 8
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 8
- 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 7
- ADFCQWZHKCXPAJ-UHFFFAOYSA-N indofine Natural products C1=CC(O)=CC=C1C1CC2=CC=C(O)C=C2OC1 ADFCQWZHKCXPAJ-UHFFFAOYSA-N 0.000 description 7
- 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 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
- 239000012043 crude product Substances 0.000 description 5
- 235000007240 daidzein Nutrition 0.000 description 5
- 235000019126 equol Nutrition 0.000 description 5
- 238000001953 recrystallisation 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
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000010511 deprotection reaction Methods 0.000 description 4
- RTRZOHKLISMNRD-UHFFFAOYSA-N isoflavanone Chemical class C1OC2=CC=CC=C2C(=O)C1C1=CC=CC=C1 RTRZOHKLISMNRD-UHFFFAOYSA-N 0.000 description 4
- GOMNOOKGLZYEJT-UHFFFAOYSA-N isoflavone Chemical compound C=1OC2=CC=CC=C2C(=O)C=1C1=CC=CC=C1 GOMNOOKGLZYEJT-UHFFFAOYSA-N 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- PPYFYRMMSWPNRA-FUHWJXTLSA-N [(3r,4s)-4-hydroxy-3-(4-methoxyphenyl)-3,4-dihydro-2h-chromen-7-yl] acetate Chemical compound C1=CC(OC)=CC=C1[C@H]1[C@H](O)C2=CC=C(OC(C)=O)C=C2OC1 PPYFYRMMSWPNRA-FUHWJXTLSA-N 0.000 description 3
- UGLVZZWYSMIGRD-UHFFFAOYSA-N [3-(4-acetyloxy-3-methoxyphenyl)-8-methyl-2h-chromen-7-yl] acetate Chemical compound C1=C(OC(C)=O)C(OC)=CC(C=2COC3=C(C)C(OC(C)=O)=CC=C3C=2)=C1 UGLVZZWYSMIGRD-UHFFFAOYSA-N 0.000 description 3
- OGGAOARBFFXXGN-UHFFFAOYSA-N [3-(4-acetyloxy-3-methoxyphenyl)-8-methyl-4-oxochromen-7-yl] 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 OGGAOARBFFXXGN-UHFFFAOYSA-N 0.000 description 3
- GSBGEARGKSAVIE-UHFFFAOYSA-N [4-(7-acetyloxy-4-hydroxy-8-methyl-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(C)=C2OC1 GSBGEARGKSAVIE-UHFFFAOYSA-N 0.000 description 3
- GSBGEARGKSAVIE-PKOBYXMFSA-N [4-[(3r,4s)-7-acetyloxy-4-hydroxy-8-methyl-3,4-dihydro-2h-chromen-3-yl]phenyl] acetate Chemical compound C1=CC(OC(=O)C)=CC=C1[C@H]1[C@H](O)C2=CC=C(OC(C)=O)C(C)=C2OC1 GSBGEARGKSAVIE-PKOBYXMFSA-N 0.000 description 3
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 239000002207 metabolite Substances 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
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- GRFPOPIKLJOMRN-NQQJLSKUSA-N OC1=CC=C2C(C(COC2=C1)C1=CC=CC=C1)O.OC1=CC=C2[C@H]([C@@H](COC2=C1)C1=CC=CC=C1)O Chemical compound OC1=CC=C2C(C(COC2=C1)C1=CC=CC=C1)O.OC1=CC=C2[C@H]([C@@H](COC2=C1)C1=CC=CC=C1)O GRFPOPIKLJOMRN-NQQJLSKUSA-N 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
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 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
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 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
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
- PWGZLQCRLSPFLS-OXJNMPFZSA-N [(3r,4s)-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([C@H]2[C@@H](C3=CC=C(OC(C)=O)C=C3OC2)O)=C1 PWGZLQCRLSPFLS-OXJNMPFZSA-N 0.000 description 1
- ISLUWCQSNPONMM-FUHWJXTLSA-N [(3r,4s)-4-hydroxy-3-(3-methoxyphenyl)-3,4-dihydro-2h-chromen-7-yl] acetate Chemical compound COC1=CC=CC([C@H]2[C@@H](C3=CC=C(OC(C)=O)C=C3OC2)O)=C1 ISLUWCQSNPONMM-FUHWJXTLSA-N 0.000 description 1
- GXEBGLSUJQSKHT-UHFFFAOYSA-N [3-(3-acetyloxyphenyl)-2h-chromen-7-yl] acetate Chemical compound CC(=O)OC1=CC=CC(C=2COC3=CC(OC(C)=O)=CC=C3C=2)=C1 GXEBGLSUJQSKHT-UHFFFAOYSA-N 0.000 description 1
- ISDRGEJSGAELLV-UHFFFAOYSA-N [3-(3-acetyloxyphenyl)-4-hydroxy-8-methyl-3,4-dihydro-2h-chromen-7-yl] acetate Chemical compound CC(=O)OC1=CC=CC(C2C(C3=CC=C(OC(C)=O)C(C)=C3OC2)O)=C1.CC(=O)OC1=CC=CC(C2C(C3=CC=C(OC(C)=O)C(C)=C3OC2)O)=C1 ISDRGEJSGAELLV-UHFFFAOYSA-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
- JULJSBKKPPJBCQ-UHFFFAOYSA-N [3-(3-acetyloxyphenyl)-8-methyl-2h-chromen-7-yl] acetate Chemical compound CC(=O)OC1=CC=CC(C=2COC3=C(C)C(OC(C)=O)=CC=C3C=2)=C1 JULJSBKKPPJBCQ-UHFFFAOYSA-N 0.000 description 1
- QVICXSCQOZLEAH-UHFFFAOYSA-N [3-(3-acetyloxyphenyl)-8-methyl-4-oxochromen-7-yl] acetate Chemical compound CC(=O)OC1=CC=CC(C=2C(C3=CC=C(OC(C)=O)C(C)=C3OC=2)=O)=C1 QVICXSCQOZLEAH-UHFFFAOYSA-N 0.000 description 1
- ZAKKBRIQGBHHJO-UHFFFAOYSA-N [3-(3-methoxyphenyl)-2h-chromen-7-yl] acetate Chemical compound COC1=CC=CC(C=2COC3=CC(OC(C)=O)=CC=C3C=2)=C1 ZAKKBRIQGBHHJO-UHFFFAOYSA-N 0.000 description 1
- NYGQCBXPZGWSMG-UHFFFAOYSA-N [3-(3-methoxyphenyl)-4-oxochromen-7-yl] acetate Chemical compound COC1=CC=CC(C=2C(C3=CC=C(OC(C)=O)C=C3OC=2)=O)=C1.COC1=CC=CC(C=2C(C3=CC=C(OC(C)=O)C=C3OC=2)=O)=C1 NYGQCBXPZGWSMG-UHFFFAOYSA-N 0.000 description 1
- WBQKITGPAIPQGR-UHFFFAOYSA-N [3-(3-methoxyphenyl)-4-oxochromen-7-yl] acetate Chemical compound COC1=CC=CC(C=2C(C3=CC=C(OC(C)=O)C=C3OC=2)=O)=C1 WBQKITGPAIPQGR-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
- ZXGPFJHKAAHHII-UHFFFAOYSA-N [3-(4-acetyloxy-3-methoxyphenyl)-4-hydroxy-8-methyl-3,4-dihydro-2H-chromen-7-yl] acetate Chemical compound C(C)(=O)OC1=C(C=C(C2COC3=C(C(=CC=C3C2O)OC(C)=O)C)C=C1)OC.C(C)(=O)OC1=C(C=C(C2COC3=C(C(=CC=C3C2O)OC(C)=O)C)C=C1)OC ZXGPFJHKAAHHII-UHFFFAOYSA-N 0.000 description 1
- XUHSPCTYNNOING-UHFFFAOYSA-N [3-(4-methoxyphenyl)-8-methyl-2h-chromen-7-yl] acetate Chemical compound C1=CC(OC)=CC=C1C1=CC2=CC=C(OC(C)=O)C(C)=C2OC1 XUHSPCTYNNOING-UHFFFAOYSA-N 0.000 description 1
- FGCYEZBJWSCUSF-UHFFFAOYSA-N [4-(7,8-diacetyloxy-2h-chromen-3-yl)phenyl] acetate Chemical compound C1=CC(OC(=O)C)=CC=C1C1=CC2=CC=C(OC(C)=O)C(OC(C)=O)=C2OC1 FGCYEZBJWSCUSF-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
- ZYOIKAQKYCKLAX-UHFFFAOYSA-N [4-hydroxy-3-(4-methoxyphenyl)-8-methyl-3,4-dihydro-2H-chromen-7-yl] acetate Chemical compound C(C)(=O)OC1=CC=C2C(C(COC2=C1C)C1=CC=C(C=C1)OC)O.C(C)(=O)OC1=CC=C2C(C(COC2=C1C)C1=CC=C(C=C1)OC)O ZYOIKAQKYCKLAX-UHFFFAOYSA-N 0.000 description 1
- RDANRSWRWLQCSQ-UHFFFAOYSA-N [8-acetyloxy-3-(4-methoxyphenyl)-4-oxochromen-7-yl] acetate Chemical compound C1=CC(OC)=CC=C1C1=COC2=C(OC(C)=O)C(OC(C)=O)=CC=C2C1=O RDANRSWRWLQCSQ-UHFFFAOYSA-N 0.000 description 1
- ZROWDXDBMFVGFX-UHFFFAOYSA-N [8-acetyloxy-3-(4-methoxyphenyl)-4-oxochromen-7-yl] acetate;[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.C1=CC(OC)=CC=C1C1=COC2=C(OC(C)=O)C(OC(C)=O)=CC=C2C1=O ZROWDXDBMFVGFX-UHFFFAOYSA-N 0.000 description 1
- WFVAMCNYBITPBJ-UHFFFAOYSA-N acetic acid (4-oxo-3-phenyl-1-benzopyran-7-yl) ester Chemical compound C=1C(OC(=O)C)=CC=C(C2=O)C=1OC=C2C1=CC=CC=C1 WFVAMCNYBITPBJ-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
- 230000008901 benefit Effects 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 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
- 230000004071 biological effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 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
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000011210 chromatographic step Methods 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 239000000428 dust 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
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 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
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 239000000543 intermediate Substances 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
- 125000004388 isoflavanoid group Chemical group 0.000 description 1
- 238000002955 isolation Methods 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
- 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
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000003128 phytoestrogenic effect Effects 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
- 239000002244 precipitate Substances 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
- 238000000746 purification Methods 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
- 238000001228 spectrum Methods 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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPP8685A AUPP868599A0 (en) | 1999-02-15 | 1999-02-15 | Production of isoflavone derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200106502B true ZA200106502B (en) | 2005-05-09 |
Family
ID=3812886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200106502A ZA200106502B (en) | 1999-02-15 | 2001-08-07 | Production of isoflavone derivatives. |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US20050143588A1 (de) |
| EP (1) | EP1153020A4 (de) |
| JP (1) | JP2002537295A (de) |
| CN (1) | CN100564370C (de) |
| AU (2) | AUPP868599A0 (de) |
| BR (1) | BR0008222A (de) |
| CA (1) | CA2362819C (de) |
| CZ (1) | CZ20012920A3 (de) |
| HK (1) | HK1041883B (de) |
| HU (1) | HUP0105218A3 (de) |
| IL (2) | IL144008A0 (de) |
| NO (1) | NO327749B1 (de) |
| NZ (1) | NZ538323A (de) |
| TR (1) | TR200102367T2 (de) |
| WO (1) | WO2000049009A1 (de) |
| ZA (1) | ZA200106502B (de) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5830887A (en) * | 1992-05-19 | 1998-11-03 | Novogen Research Pty. Ltd. | Health supplements containing phyto-oestrogens, analogues or metabolites thereof |
| US6340703B1 (en) * | 1997-05-01 | 2002-01-22 | Novogen, Inc. | Treatment or prevention of 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 |
| CN1646119A (zh) * | 2002-04-09 | 2005-07-27 | 诺沃根研究有限公司 | 涉及异黄－3－烯和异黄烷结构的治疗方法和组合物 |
| CN1681386B (zh) * | 2002-07-24 | 2010-05-26 | 儿童医院医疗中心 | 含有对映体牛尿酚的组合物和产物及其制备方法 |
| US8668914B2 (en) | 2002-07-24 | 2014-03-11 | Brigham Young University | Use of equol for treating skin diseases |
| WO2004039327A2 (en) | 2002-10-29 | 2004-05-13 | Colorado State University Research Foundation | Use of equol for treating androgen mediated diseases |
| AU2003255232A1 (en) * | 2002-08-07 | 2004-02-25 | University Of Mississippi | Antigiardial agents and use thereof |
| AU2003257264B2 (en) * | 2002-09-06 | 2007-09-13 | Novogen Research Pty Ltd | Repair of DNA mutagenic damage |
| AU2002951271A0 (en) * | 2002-09-06 | 2002-09-19 | Novogen Research Pty Ltd | Repair of dna mutagenic damage |
| JP2006508058A (ja) * | 2002-09-23 | 2006-03-09 | ノボジェン・リサーチ・プロプライエタリー・リミテッド | 皮膚光老化および光線性損傷の治療 |
| 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 |
| CN101056868B (zh) | 2004-09-21 | 2012-05-02 | 马休爱德华兹股份有限公司 | 取代的苯并二氢吡喃衍生物、药物及其在治疗中的应用 |
| EP1809618B1 (de) | 2004-09-21 | 2013-07-17 | Marshall Edwards, Inc. | Chromanderivate, medikamente und anwendung in der therapie |
| 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 (de) | 2008-06-13 | 2009-12-16 | Haelan Schweiz GmbH | Zusammensetzungen enthaltend Equol |
| 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 |
| 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 |
| JP6013349B2 (ja) | 2010-11-01 | 2016-10-25 | メイ ファーマ, インク.Mei Pharma, Inc. | 癌の処置のためのイソフラボノイド化合物および方法 |
| WO2012097858A1 (en) * | 2011-01-20 | 2012-07-26 | Merck Patent Gmbh | Polymerisable compounds and the use thereof in liquid-crystal displays |
| US10420761B2 (en) | 2013-03-15 | 2019-09-24 | University Of Florida Research Foundation, Inc. | Allosteric inhibitors of 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 |
| HUE054998T2 (hu) | 2015-02-02 | 2021-10-28 | Mei Pharma Inc | Kombinációs terápiák emlõrák kezelésében való alkalmazásra |
| US10835524B2 (en) | 2015-06-24 | 2020-11-17 | University Of Florida Research Foundation, Incorporated | Compositions for the treatment of pancreatic cancer and uses thereof |
| 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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| Publication number | Priority date | Publication date | Assignee | Title |
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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 (de) * | 1973-08-01 | 1975-04-04 | ||
| JPS576427B2 (de) * | 1974-01-25 | 1982-02-04 | ||
| JPS50160483A (de) * | 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 |
| JPH0640876A (ja) * | 1992-07-23 | 1994-02-15 | Kobe Steel Ltd | 紫外線障害防御外用剤 |
| 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 |
| 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 |
| EP1057825A4 (de) * | 1998-01-27 | 2001-10-24 | Shionogi & Co | Isoflavanderivate und immunverstärkende zusammensetzungen die diese enthalten |
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1999
- 1999-02-15 AU AUPP8685A patent/AUPP868599A0/en not_active Abandoned
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- 2000-02-15 CZ CZ20012920A patent/CZ20012920A3/cs unknown
- 2000-02-15 BR BR0008222-8A patent/BR0008222A/pt not_active Application Discontinuation
- 2000-02-15 NZ NZ538323A patent/NZ538323A/en not_active IP Right Cessation
- 2000-02-15 JP JP2000599749A patent/JP2002537295A/ja active Pending
- 2000-02-15 TR TR2001/02367T patent/TR200102367T2/xx unknown
- 2000-02-15 EP EP00904727A patent/EP1153020A4/de not_active Withdrawn
- 2000-02-15 AU AU26510/00A patent/AU2651000A/en not_active Abandoned
- 2000-02-15 HU HU0105218A patent/HUP0105218A3/hu unknown
- 2000-02-15 CN CNB008038163A patent/CN100564370C/zh not_active Expired - Fee Related
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2001
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Also Published As
| Publication number | Publication date |
|---|---|
| HK1041883B (zh) | 2010-04-23 |
| EP1153020A4 (de) | 2002-08-21 |
| US20060217564A1 (en) | 2006-09-28 |
| IL144008A0 (en) | 2002-04-21 |
| NO20013945L (no) | 2001-08-14 |
| CN100564370C (zh) | 2009-12-02 |
| CZ20012920A3 (cs) | 2001-11-14 |
| HK1041883A1 (en) | 2002-07-26 |
| US20050143588A1 (en) | 2005-06-30 |
| BR0008222A (pt) | 2001-10-30 |
| JP2002537295A (ja) | 2002-11-05 |
| CA2362819C (en) | 2011-05-10 |
| CA2362819A1 (en) | 2000-08-24 |
| HUP0105218A3 (en) | 2002-10-28 |
| AUPP868599A0 (en) | 1999-03-11 |
| NO20013945D0 (no) | 2001-08-14 |
| NZ538323A (en) | 2005-10-28 |
| AU2651000A (en) | 2000-09-04 |
| WO2000049009A1 (en) | 2000-08-24 |
| IL144008A (en) | 2011-03-31 |
| CN1340048A (zh) | 2002-03-13 |
| HUP0105218A1 (hu) | 2002-07-29 |
| TR200102367T2 (tr) | 2001-11-21 |
| US7906660B2 (en) | 2011-03-15 |
| NO327749B1 (no) | 2009-09-14 |
| EP1153020A1 (de) | 2001-11-14 |
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