HU194549B - Process for producing 8-bromo-1-4-alkyl-4h-square bracket opened-1-square bracket closed-pyran-4-ones - Google Patents
Process for producing 8-bromo-1-4-alkyl-4h-square bracket opened-1-square bracket closed-pyran-4-ones Download PDFInfo
- Publication number
- HU194549B HU194549B HU823763A HU376382A HU194549B HU 194549 B HU194549 B HU 194549B HU 823763 A HU823763 A HU 823763A HU 376382 A HU376382 A HU 376382A HU 194549 B HU194549 B HU 194549B
- Authority
- HU
- Hungary
- Prior art keywords
- singlet
- phenyl
- mol
- alkyl
- methoxymethyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 25
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 51
- 150000001875 compounds Chemical class 0.000 claims description 21
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 229910000042 hydrogen bromide Inorganic materials 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 5
- 150000002431 hydrogen Chemical group 0.000 claims description 4
- ZBJJDYGJCNTNTH-UHFFFAOYSA-N Betahistine mesilate Chemical group CS(O)(=O)=O.CS(O)(=O)=O.CNCCC1=CC=CC=N1 ZBJJDYGJCNTNTH-UHFFFAOYSA-N 0.000 claims description 3
- 125000004076 pyridyl group Chemical group 0.000 claims description 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 239000000575 pesticide Substances 0.000 abstract description 2
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 abstract 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 30
- 238000005481 NMR spectroscopy Methods 0.000 description 25
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 24
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 239000000203 mixture Substances 0.000 description 24
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 239000000047 product Substances 0.000 description 17
- -1 polyoxymethylene Polymers 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 15
- 238000002844 melting Methods 0.000 description 13
- 230000008018 melting Effects 0.000 description 13
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 239000007858 starting material Substances 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- 238000009835 boiling Methods 0.000 description 10
- 239000002244 precipitate Substances 0.000 description 10
- 238000010992 reflux Methods 0.000 description 10
- IFCGCPVGNNQERD-UHFFFAOYSA-N methyl 2-methoxy-3-(methoxymethyl)benzoate Chemical compound COCC1=CC=CC(C(=O)OC)=C1OC IFCGCPVGNNQERD-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 8
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 8
- 238000000926 separation method Methods 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 239000000543 intermediate Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- MGADZUXDNSDTHW-UHFFFAOYSA-N 2H-pyran Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 description 6
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 6
- AUPQTLYTDMSQBO-UHFFFAOYSA-N 1-[2-hydroxy-3-(methoxymethyl)phenyl]ethanone Chemical compound COCC1=CC=CC(C(C)=O)=C1O AUPQTLYTDMSQBO-UHFFFAOYSA-N 0.000 description 5
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 239000012312 sodium hydride Substances 0.000 description 5
- 229910000104 sodium hydride Inorganic materials 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Substances BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 3
- 229930040373 Paraformaldehyde Natural products 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- OTAFHZMPRISVEM-UHFFFAOYSA-N chromone Chemical compound C1=CC=C2C(=O)C=COC2=C1 OTAFHZMPRISVEM-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- RBBOWEDMXHTEPA-UHFFFAOYSA-N hexane;toluene Chemical compound CCCCCC.CC1=CC=CC=C1 RBBOWEDMXHTEPA-UHFFFAOYSA-N 0.000 description 3
- WWWCQWYKUZAHLY-UHFFFAOYSA-N methyl 2-methoxy-3-methylbenzoate Chemical compound COC(=O)C1=CC=CC(C)=C1OC WWWCQWYKUZAHLY-UHFFFAOYSA-N 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229920006324 polyoxymethylene Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- LKARHMGTFAUGRN-UHFFFAOYSA-N 1-[2-hydroxy-3-(methoxymethyl)-5-methylphenyl]ethanone Chemical compound COCC1=CC(C)=CC(C(C)=O)=C1O LKARHMGTFAUGRN-UHFFFAOYSA-N 0.000 description 2
- SGTXDYCZTVIBLI-UHFFFAOYSA-N 1-[2-hydroxy-5-methoxy-3-(methoxymethyl)phenyl]ethanone Chemical compound COCC1=CC(OC)=CC(C(C)=O)=C1O SGTXDYCZTVIBLI-UHFFFAOYSA-N 0.000 description 2
- RDLXSIDDICACCE-UHFFFAOYSA-N 1-[2-methoxy-3-(methoxymethyl)phenyl]butane-1,3-dione Chemical compound COCC1=CC=CC(C(=O)CC(C)=O)=C1OC RDLXSIDDICACCE-UHFFFAOYSA-N 0.000 description 2
- OXEFQXTUCAUBLU-UHFFFAOYSA-N 1-[2-methoxy-3-(methoxymethyl)phenyl]ethanone Chemical compound COCC1=CC=CC(C(C)=O)=C1OC OXEFQXTUCAUBLU-UHFFFAOYSA-N 0.000 description 2
- JECYUBVRTQDVAT-UHFFFAOYSA-N 2-acetylphenol Chemical compound CC(=O)C1=CC=CC=C1O JECYUBVRTQDVAT-UHFFFAOYSA-N 0.000 description 2
- CXAXQHDTUXCBPH-UHFFFAOYSA-N 2-methoxy-3-(methoxymethyl)benzoic acid Chemical compound COCC1=CC=CC(C(O)=O)=C1OC CXAXQHDTUXCBPH-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- IQZLUWLMQNGTIW-UHFFFAOYSA-N acetoveratrone Chemical compound COC1=CC=C(C(C)=O)C=C1OC IQZLUWLMQNGTIW-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229950005499 carbon tetrachloride Drugs 0.000 description 2
- 238000007265 chloromethylation reaction Methods 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 125000002587 enol group Chemical group 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- OFNCKBSGHOIZJC-UHFFFAOYSA-N methyl 3-(bromomethyl)-2-methoxybenzoate Chemical compound COC(=O)C1=CC=CC(CBr)=C1OC OFNCKBSGHOIZJC-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 1
- JLIDRDJNLAWIKT-UHFFFAOYSA-N 1,2-dimethyl-3h-benzo[e]indole Chemical compound C1=CC=CC2=C(C(=C(C)N3)C)C3=CC=C21 JLIDRDJNLAWIKT-UHFFFAOYSA-N 0.000 description 1
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 description 1
- MLIBGOFSXXWRIY-UHFFFAOYSA-N 1-(2-hydroxy-5-methoxyphenyl)ethanone Chemical compound COC1=CC=C(O)C(C(C)=O)=C1 MLIBGOFSXXWRIY-UHFFFAOYSA-N 0.000 description 1
- BAYUSCHCCGXLAY-UHFFFAOYSA-N 1-(3-methoxyphenyl)ethanone Chemical compound COC1=CC=CC(C(C)=O)=C1 BAYUSCHCCGXLAY-UHFFFAOYSA-N 0.000 description 1
- BUZYGTVTZYSBCU-UHFFFAOYSA-N 1-(4-chlorophenyl)ethanone Chemical compound CC(=O)C1=CC=C(Cl)C=C1 BUZYGTVTZYSBCU-UHFFFAOYSA-N 0.000 description 1
- ITBZVCBNKOBIKP-UHFFFAOYSA-N 1-[2-hydroxy-3-(methoxymethyl)phenyl]-3-phenylpropane-1,3-dione Chemical compound OC1=C(C=CC=C1COC)C(CC(=O)C1=CC=CC=C1)=O ITBZVCBNKOBIKP-UHFFFAOYSA-N 0.000 description 1
- SATOCOOGWNYXCF-UHFFFAOYSA-N 1-[2-hydroxy-3-(methoxymethyl)phenyl]-4-phenylbutane-1,3-dione Chemical compound COCC1=CC=CC(C(=O)CC(=O)CC=2C=CC=CC=2)=C1O SATOCOOGWNYXCF-UHFFFAOYSA-N 0.000 description 1
- ZAKKEKMTESQSPX-UHFFFAOYSA-N 1-[3,5-bis(chloromethyl)-2-hydroxyphenyl]ethanone Chemical compound CC(=O)C1=CC(CCl)=CC(CCl)=C1O ZAKKEKMTESQSPX-UHFFFAOYSA-N 0.000 description 1
- AOZFQWXSERPKHQ-UHFFFAOYSA-N 1-[3-(chloromethyl)-2-hydroxy-5-methylphenyl]ethanone Chemical compound CC(=O)C1=CC(C)=CC(CCl)=C1O AOZFQWXSERPKHQ-UHFFFAOYSA-N 0.000 description 1
- NEQYIZFEXXWDEO-UHFFFAOYSA-N 1-[3-(chloromethyl)-2-hydroxyphenyl]ethanone Chemical compound CC(=O)C1=CC=CC(CCl)=C1O NEQYIZFEXXWDEO-UHFFFAOYSA-N 0.000 description 1
- JNXISTMARPWKRJ-UHFFFAOYSA-N 1-[5-(chloromethyl)-2-hydroxyphenyl]ethanone Chemical compound CC(=O)C1=CC(CCl)=CC=C1O JNXISTMARPWKRJ-UHFFFAOYSA-N 0.000 description 1
- HVMPHGHFITZYDQ-UHFFFAOYSA-N 1-[5-chloro-2-hydroxy-3-(methoxymethyl)phenyl]ethanone Chemical compound COCC1=CC(Cl)=CC(C(C)=O)=C1O HVMPHGHFITZYDQ-UHFFFAOYSA-N 0.000 description 1
- WWNJCGKNKZXVIS-UHFFFAOYSA-N 1-[5-chloro-3-(chloromethyl)-2-hydroxyphenyl]ethanone Chemical compound CC(=O)C1=CC(Cl)=CC(CCl)=C1O WWNJCGKNKZXVIS-UHFFFAOYSA-N 0.000 description 1
- WXLLZEFYWRGYKT-UHFFFAOYSA-N 1-cyclohexyl-3-[2-hydroxy-3-(methoxymethyl)phenyl]propane-1,3-dione Chemical compound COCC1=CC=CC(C(=O)CC(=O)C2CCCCC2)=C1O WXLLZEFYWRGYKT-UHFFFAOYSA-N 0.000 description 1
- QMDUEBURHKSKDG-UHFFFAOYSA-N 1-pyridin-3-ylethanol Chemical compound CC(O)C1=CC=CN=C1 QMDUEBURHKSKDG-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- IEMMBWWQXVXBEU-UHFFFAOYSA-N 2-acetylfuran Chemical compound CC(=O)C1=CC=CO1 IEMMBWWQXVXBEU-UHFFFAOYSA-N 0.000 description 1
- XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 description 1
- UYDGECQHZQNTQS-UHFFFAOYSA-N 2-amino-4,6-dimethylpyridine-3-carboxamide Chemical compound CC1=CC(C)=C(C(N)=O)C(N)=N1 UYDGECQHZQNTQS-UHFFFAOYSA-N 0.000 description 1
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- YNOOKZNZFSBIHN-UHFFFAOYSA-N 2-methoxy-3-(methoxymethyl)benzoyl chloride Chemical compound COCC1=CC=CC(C(Cl)=O)=C1OC YNOOKZNZFSBIHN-UHFFFAOYSA-N 0.000 description 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 1
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 description 1
- DZCTYFCCOGXULA-UHFFFAOYSA-N 3-bromochromen-2-one Chemical class C1=CC=C2OC(=O)C(Br)=CC2=C1 DZCTYFCCOGXULA-UHFFFAOYSA-N 0.000 description 1
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 description 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- MQGPSCMMNJKMHQ-UHFFFAOYSA-N 7-hydroxyflavone Chemical class C=1C(O)=CC=C(C(C=2)=O)C=1OC=2C1=CC=CC=C1 MQGPSCMMNJKMHQ-UHFFFAOYSA-N 0.000 description 1
- YSBYLFYTEYENPF-UHFFFAOYSA-N 8-(bromomethyl)-2-(4-methylphenyl)chromen-4-one Chemical compound C1=CC(C)=CC=C1C1=CC(=O)C2=CC=CC(CBr)=C2O1 YSBYLFYTEYENPF-UHFFFAOYSA-N 0.000 description 1
- DJIQFUKGEMJGKZ-UHFFFAOYSA-N 8-(bromomethyl)-2-methylchromen-4-one Chemical compound C1=CC(CBr)=C2OC(C)=CC(=O)C2=C1 DJIQFUKGEMJGKZ-UHFFFAOYSA-N 0.000 description 1
- VFNAAUOSXUBYFV-UHFFFAOYSA-N 8-(bromomethyl)-2-phenylchromen-4-one Chemical compound BrCC1=CC=CC(C(C=2)=O)=C1OC=2C1=CC=CC=C1 VFNAAUOSXUBYFV-UHFFFAOYSA-N 0.000 description 1
- OBESSGZVMSYYHW-UHFFFAOYSA-N 8-(bromomethyl)-6-methoxy-2-phenylchromen-4-one Chemical compound C=1C(=O)C2=CC(OC)=CC(CBr)=C2OC=1C1=CC=CC=C1 OBESSGZVMSYYHW-UHFFFAOYSA-N 0.000 description 1
- GGHANFCKLFDEIJ-UHFFFAOYSA-N 8-(bromomethyl)-6-methyl-2-phenylchromen-4-one Chemical compound C=1C(=O)C2=CC(C)=CC(CBr)=C2OC=1C1=CC=CC=C1 GGHANFCKLFDEIJ-UHFFFAOYSA-N 0.000 description 1
- ZPSZTJUSHMIKRF-UHFFFAOYSA-N 8-(bromomethyl)chromen-4-one Chemical class BrCC1=CC=CC=2C(C=COC=21)=O ZPSZTJUSHMIKRF-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- CTGGJXNFCDMEME-UHFFFAOYSA-N COC1=CC(CCl)=C(O)C(C(C)=O)=C1 Chemical compound COC1=CC(CCl)=C(O)C(C(C)=O)=C1 CTGGJXNFCDMEME-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- NOTFZGFABLVTIG-UHFFFAOYSA-N Cyclohexylethyl acetate Chemical compound CC(=O)OCCC1CCCCC1 NOTFZGFABLVTIG-UHFFFAOYSA-N 0.000 description 1
- KBEBGUQPQBELIU-CMDGGOBGSA-N Ethyl cinnamate Chemical compound CCOC(=O)\C=C\C1=CC=CC=C1 KBEBGUQPQBELIU-CMDGGOBGSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 235000019502 Orange oil Nutrition 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- DULCUDSUACXJJC-UHFFFAOYSA-N benzeneacetic acid ethyl ester Natural products CCOC(=O)CC1=CC=CC=C1 DULCUDSUACXJJC-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
- VJGNLOIQCWLBJR-UHFFFAOYSA-M benzyl(tributyl)azanium;chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CC1=CC=CC=C1 VJGNLOIQCWLBJR-UHFFFAOYSA-M 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000005997 bromomethyl group Chemical group 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 1
- JJOYCHKVKWDMEA-UHFFFAOYSA-N ethyl cyclohexanecarboxylate Chemical compound CCOC(=O)C1CCCCC1 JJOYCHKVKWDMEA-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- WHSXTWFYRGOBGO-UHFFFAOYSA-N o-cresotic acid Natural products CC1=CC=CC(C(O)=O)=C1O WHSXTWFYRGOBGO-UHFFFAOYSA-N 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- NODGRWCMFMEGJH-UHFFFAOYSA-N p-ethylacetophenone Chemical compound CCC1=CC=C(C(C)=O)C=C1 NODGRWCMFMEGJH-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- IMACFCSSMIZSPP-UHFFFAOYSA-N phenacyl chloride Chemical compound ClCC(=O)C1=CC=CC=C1 IMACFCSSMIZSPP-UHFFFAOYSA-N 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229950005792 tenoate Drugs 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/21—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups
-
- 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
-
- 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
- C07D311/28—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 2 only
- C07D311/30—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 2 only not hydrogenated in the hetero ring, e.g. flavones
-
- 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
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrane Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8122019A FR2516921A1 (fr) | 1981-11-25 | 1981-11-25 | Haloalkyl-8-4h-(1) benzopyran-4-ones, et procedes de preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU194549B true HU194549B (en) | 1988-02-29 |
Family
ID=9264330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU823763A HU194549B (en) | 1981-11-25 | 1982-11-23 | Process for producing 8-bromo-1-4-alkyl-4h-square bracket opened-1-square bracket closed-pyran-4-ones |
Country Status (24)
| Country | Link |
|---|---|
| EP (1) | EP0080419B1 (enExample) |
| JP (1) | JPS5896038A (enExample) |
| AR (1) | AR243249A1 (enExample) |
| AT (1) | ATE49760T1 (enExample) |
| AU (1) | AU563066B2 (enExample) |
| CA (1) | CA1197511A (enExample) |
| CS (1) | CS236696B2 (enExample) |
| DD (1) | DD204920A5 (enExample) |
| DE (1) | DE3280092D1 (enExample) |
| DK (1) | DK166778B1 (enExample) |
| ES (1) | ES8308322A1 (enExample) |
| FR (1) | FR2516921A1 (enExample) |
| HU (1) | HU194549B (enExample) |
| IE (1) | IE56916B1 (enExample) |
| IL (1) | IL67290A0 (enExample) |
| IN (1) | IN158942B (enExample) |
| MA (1) | MA19649A1 (enExample) |
| NO (1) | NO162463C (enExample) |
| NZ (1) | NZ202595A (enExample) |
| OA (1) | OA07256A (enExample) |
| PT (2) | PT75886A (enExample) |
| SU (2) | SU1189344A3 (enExample) |
| YU (1) | YU43808B (enExample) |
| ZA (1) | ZA828435B (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5002603A (en) * | 1989-12-04 | 1991-03-26 | Board Of Trustees Operating Michigan State University | Method and compositions for stimulating vesicular-arbuscular mycorrhizal fungi |
| WO1998027080A1 (en) * | 1996-12-19 | 1998-06-25 | Agrevo Uk Limited | Chromones useful as fungicides |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1270567B (de) * | 1961-05-19 | 1968-06-20 | Klinge Co Chem Pharm Fab | Verfahren zur Herstellung von basisch substituierten Flavonen |
| HU168753B (enExample) * | 1974-05-03 | 1976-07-28 | ||
| FR2326919A2 (fr) * | 1975-10-10 | 1977-05-06 | Lipha | Nouveaux acides inferieurs substitues par un radical chromonyle, leurs derives et leurs applications |
| FR2291745A1 (fr) * | 1974-11-20 | 1976-06-18 | Lipha | Nouveaux acides inferieurs substitues par un radical chromonyl, leurs derives et leurs applications |
| US3966770A (en) * | 1975-03-25 | 1976-06-29 | Smithkline Corporation | 4-Hydroxy-α-[(3,4-methylenedioxyphenyl)isopropylaminoethyl]-3-(methylsulfonylmethyl)benzyl alcohol |
| FR2392018A1 (fr) * | 1977-05-27 | 1978-12-22 | Seuref Ag | Derives de la 2,3-diphenyl-chromone, leur procede de preparation et leur application therapeutique |
| FR2517142A1 (fr) * | 1981-11-20 | 1983-05-27 | Efcis | Bascule bistable a stockage non volatil et a repositionnement statique |
-
1981
- 1981-11-25 FR FR8122019A patent/FR2516921A1/fr active Granted
-
1982
- 1982-11-16 ZA ZA828435A patent/ZA828435B/xx unknown
- 1982-11-17 IL IL67290A patent/IL67290A0/xx not_active IP Right Cessation
- 1982-11-18 IE IE2753/82A patent/IE56916B1/en not_active IP Right Cessation
- 1982-11-18 IN IN847/DEL/82A patent/IN158942B/en unknown
- 1982-11-19 AU AU90728/82A patent/AU563066B2/en not_active Ceased
- 1982-11-23 PT PT75886A patent/PT75886A/pt unknown
- 1982-11-23 PT PT75885A patent/PT75885A/pt unknown
- 1982-11-23 HU HU823763A patent/HU194549B/hu not_active IP Right Cessation
- 1982-11-24 NZ NZ202595A patent/NZ202595A/en unknown
- 1982-11-24 AT AT82402136T patent/ATE49760T1/de not_active IP Right Cessation
- 1982-11-24 NO NO823939A patent/NO162463C/no unknown
- 1982-11-24 ES ES517636A patent/ES8308322A1/es not_active Expired
- 1982-11-24 MA MA19862A patent/MA19649A1/fr unknown
- 1982-11-24 SU SU823515153A patent/SU1189344A3/ru active
- 1982-11-24 EP EP82402136A patent/EP0080419B1/fr not_active Expired - Lifetime
- 1982-11-24 DE DE8282402136T patent/DE3280092D1/de not_active Expired - Lifetime
- 1982-11-24 CS CS828425A patent/CS236696B2/cs unknown
- 1982-11-24 DK DK522982A patent/DK166778B1/da not_active IP Right Cessation
- 1982-11-25 JP JP57205581A patent/JPS5896038A/ja active Granted
- 1982-11-25 YU YU2648/82A patent/YU43808B/xx unknown
- 1982-11-25 CA CA000416341A patent/CA1197511A/fr not_active Expired
- 1982-11-25 DD DD82245220A patent/DD204920A5/de unknown
- 1982-11-25 OA OA57849A patent/OA07256A/xx unknown
- 1982-11-25 AR AR82291414A patent/AR243249A1/es active
-
1983
- 1983-09-20 SU SU833644104A patent/SU1232146A3/ru active
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HU90 | Patent valid on 900628 | ||
| HMM4 | Cancellation of final prot. due to non-payment of fee |