JPS61501089A - 環式ジスルホン酸エステル化合物 - Google Patents
環式ジスルホン酸エステル化合物Info
- Publication number
- JPS61501089A JPS61501089A JP60500579A JP50057985A JPS61501089A JP S61501089 A JPS61501089 A JP S61501089A JP 60500579 A JP60500579 A JP 60500579A JP 50057985 A JP50057985 A JP 50057985A JP S61501089 A JPS61501089 A JP S61501089A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- compound according
- tables
- item
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002253 acid Substances 0.000 title claims description 30
- 125000004122 cyclic group Chemical group 0.000 title claims description 28
- -1 ester compounds Chemical class 0.000 title claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 56
- 206010028980 Neoplasm Diseases 0.000 claims description 35
- 239000000126 substance Substances 0.000 claims description 31
- 150000002148 esters Chemical class 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 26
- 238000006243 chemical reaction Methods 0.000 claims description 23
- 241001465754 Metazoa Species 0.000 claims description 19
- 201000011510 cancer Diseases 0.000 claims description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 15
- 208000003747 lymphoid leukemia Diseases 0.000 claims description 15
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims description 14
- 208000028018 Lymphocytic leukaemia Diseases 0.000 claims description 14
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 13
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 11
- 229910052709 silver Inorganic materials 0.000 claims description 11
- 239000004332 silver Substances 0.000 claims description 11
- 206010006187 Breast cancer Diseases 0.000 claims description 9
- 208000026310 Breast neoplasm Diseases 0.000 claims description 9
- 206010033128 Ovarian cancer Diseases 0.000 claims description 8
- 206010061535 Ovarian neoplasm Diseases 0.000 claims description 8
- 230000037396 body weight Effects 0.000 claims description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 7
- ZXSQEZNORDWBGZ-UHFFFAOYSA-N 1,3-dihydropyrrolo[2,3-b]pyridin-2-one Chemical compound C1=CN=C2NC(=O)CC2=C1 ZXSQEZNORDWBGZ-UHFFFAOYSA-N 0.000 claims description 6
- 238000005804 alkylation reaction Methods 0.000 claims description 6
- LKZMBDSASOBTPN-UHFFFAOYSA-L silver carbonate Substances [Ag].[O-]C([O-])=O LKZMBDSASOBTPN-UHFFFAOYSA-L 0.000 claims description 6
- 229910001958 silver carbonate Inorganic materials 0.000 claims description 6
- 230000001588 bifunctional effect Effects 0.000 claims description 5
- 201000001441 melanoma Diseases 0.000 claims description 5
- 239000000376 reactant Substances 0.000 claims description 4
- 150000003512 tertiary amines Chemical class 0.000 claims description 4
- 230000029936 alkylation Effects 0.000 claims description 3
- 239000012048 reactive intermediate Substances 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 2
- 230000001093 anti-cancer Effects 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 239000007928 intraperitoneal injection Substances 0.000 claims 3
- 206010027476 Metastases Diseases 0.000 claims 1
- 239000003925 fat Substances 0.000 claims 1
- 238000007917 intracranial administration Methods 0.000 claims 1
- 230000009401 metastasis Effects 0.000 claims 1
- 239000007929 subcutaneous injection Substances 0.000 claims 1
- 238000010254 subcutaneous injection Methods 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 54
- 239000000047 product Substances 0.000 description 38
- 239000000243 solution Substances 0.000 description 33
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 27
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 27
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 24
- 239000000203 mixture Substances 0.000 description 20
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 16
- 239000002904 solvent Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000003814 drug Substances 0.000 description 13
- 229940079593 drug Drugs 0.000 description 13
- 238000011282 treatment Methods 0.000 description 13
- 239000013078 crystal Substances 0.000 description 12
- 239000000843 powder Substances 0.000 description 10
- 238000010992 reflux Methods 0.000 description 10
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 9
- 108020004414 DNA Proteins 0.000 description 9
- 210000004027 cell Anatomy 0.000 description 9
- 238000001035 drying Methods 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 230000004083 survival effect Effects 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000006228 supernatant Substances 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- DJSXAWRMVVSQDV-UHFFFAOYSA-L C(S(=O)(=O)[O-])S(=O)(=O)[O-].[Ag+2] Chemical compound C(S(=O)(=O)[O-])S(=O)(=O)[O-].[Ag+2] DJSXAWRMVVSQDV-UHFFFAOYSA-L 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 238000007912 intraperitoneal administration Methods 0.000 description 6
- 208000032839 leukemia Diseases 0.000 description 6
- DKZQZHQHDMVGHE-UHFFFAOYSA-N methanedisulfonyl chloride Chemical compound ClS(=O)(=O)CS(Cl)(=O)=O DKZQZHQHDMVGHE-UHFFFAOYSA-N 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- 125000000542 sulfonic acid group Chemical group 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 238000005481 NMR spectroscopy Methods 0.000 description 5
- 229940100198 alkylating agent Drugs 0.000 description 5
- 239000002168 alkylating agent Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 239000000543 intermediate Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 108090000623 proteins and genes Proteins 0.000 description 5
- 102000004169 proteins and genes Human genes 0.000 description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- RYIRMSRYCSMGJA-UHFFFAOYSA-N 1,5,2,4-dioxadithiepane 2,2,4,4-tetraoxide Chemical compound O=S1(=O)CS(=O)(=O)OCCO1 RYIRMSRYCSMGJA-UHFFFAOYSA-N 0.000 description 4
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
- 241000699670 Mus sp. Species 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- HOPRXXXSABQWAV-UHFFFAOYSA-N anhydrous collidine Natural products CC1=CC=NC(C)=C1C HOPRXXXSABQWAV-UHFFFAOYSA-N 0.000 description 4
- 230000000719 anti-leukaemic effect Effects 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical class OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 239000003610 charcoal Substances 0.000 description 4
- UTBIMNXEDGNJFE-UHFFFAOYSA-N collidine Natural products CC1=CC=C(C)C(C)=N1 UTBIMNXEDGNJFE-UHFFFAOYSA-N 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 238000000921 elemental analysis Methods 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 239000012038 nucleophile Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 238000001953 recrystallisation Methods 0.000 description 4
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 4
- 230000003595 spectral effect Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 4
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- 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 3
- 229910021607 Silver chloride Inorganic materials 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000002152 alkylating effect Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- 150000001923 cyclic compounds Chemical class 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 238000002390 rotary evaporation Methods 0.000 description 3
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 238000001308 synthesis method Methods 0.000 description 3
- 238000010189 synthetic method Methods 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 3
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 2
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 2
- GWAOOGWHPITOEY-UHFFFAOYSA-N 1,5,2,4-dioxadithiane 2,2,4,4-tetraoxide Chemical compound O=S1(=O)CS(=O)(=O)OCO1 GWAOOGWHPITOEY-UHFFFAOYSA-N 0.000 description 2
- BXXWFOGWXLJPPA-UHFFFAOYSA-N 2,3-dibromobutane Chemical compound CC(Br)C(C)Br BXXWFOGWXLJPPA-UHFFFAOYSA-N 0.000 description 2
- QSQFARNGNIZGAW-UHFFFAOYSA-N 2-methylsulfonyloxyethyl methanesulfonate Chemical compound CS(=O)(=O)OCCOS(C)(=O)=O QSQFARNGNIZGAW-UHFFFAOYSA-N 0.000 description 2
- XPMXSCXQTAOMAE-UHFFFAOYSA-N 3-methyl-1,5,2,4-dioxadithiepane 2,2,4,4-tetraoxide Chemical compound CC1S(=O)(=O)OCCOS1(=O)=O XPMXSCXQTAOMAE-UHFFFAOYSA-N 0.000 description 2
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- 241001474791 Proboscis Species 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000010936 aqueous wash Methods 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 210000000481 breast Anatomy 0.000 description 2
- 235000011089 carbon dioxide Nutrition 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- LNZMEOLVTKHUAS-UHFFFAOYSA-N cyclohexane;dichloromethane Chemical compound ClCCl.C1CCCCC1 LNZMEOLVTKHUAS-UHFFFAOYSA-N 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- UYTPUPDQBNUYGX-UHFFFAOYSA-N guanine Chemical compound O=C1NC(N)=NC2=C1N=CN2 UYTPUPDQBNUYGX-UHFFFAOYSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 2
- 230000008439 repair process Effects 0.000 description 2
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- 238000007920 subcutaneous administration Methods 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 2
- YMEQSAKKSIAHCT-UHFFFAOYSA-N trimethylsilyl chlorosulfonylmethanesulfonate Chemical compound C[Si](C)(C)OS(=O)(=O)CS(Cl)(=O)=O YMEQSAKKSIAHCT-UHFFFAOYSA-N 0.000 description 2
- 238000003828 vacuum filtration Methods 0.000 description 2
- GHPYJLCQYMAXGG-WCCKRBBISA-N (2R)-2-amino-3-(2-boronoethylsulfanyl)propanoic acid hydrochloride Chemical compound Cl.N[C@@H](CSCCB(O)O)C(O)=O GHPYJLCQYMAXGG-WCCKRBBISA-N 0.000 description 1
- APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 1
- ATWLRNODAYAMQS-UHFFFAOYSA-N 1,1-dibromopropane Chemical compound CCC(Br)Br ATWLRNODAYAMQS-UHFFFAOYSA-N 0.000 description 1
- VEFLKXRACNJHOV-UHFFFAOYSA-N 1,3-dibromopropane Chemical compound BrCCCBr VEFLKXRACNJHOV-UHFFFAOYSA-N 0.000 description 1
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- WCVOGSZTONGSQY-UHFFFAOYSA-N 2,4,6-trichloroanisole Chemical compound COC1=C(Cl)C=C(Cl)C=C1Cl WCVOGSZTONGSQY-UHFFFAOYSA-N 0.000 description 1
- BWLBGMIXKSTLSX-UHFFFAOYSA-N 2-hydroxyisobutyric acid Chemical compound CC(C)(O)C(O)=O BWLBGMIXKSTLSX-UHFFFAOYSA-N 0.000 description 1
- XSELLMOWTWIQSS-UHFFFAOYSA-N 3-methyl-1,5,2,4-dioxadithiecane 2,2,4,4-tetraoxide Chemical compound CC1S(=O)(=O)OCCCCCOS1(=O)=O XSELLMOWTWIQSS-UHFFFAOYSA-N 0.000 description 1
- VFAYXHHSHNWWGM-UHFFFAOYSA-N 3-methyl-1,5,2,4-dioxadithiocane 2,2,4,4-tetraoxide Chemical compound CC1S(=O)(=O)OCCCOS1(=O)=O VFAYXHHSHNWWGM-UHFFFAOYSA-N 0.000 description 1
- AHZVUIHKZKQRGL-UHFFFAOYSA-N 3-methyl-1,5,2,4-dioxadithionane 2,2,4,4-tetraoxide Chemical compound CC1S(=O)(=O)OCCCCOS1(=O)=O AHZVUIHKZKQRGL-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- LOFFIJMYYLJQDG-UHFFFAOYSA-N C(C)#N.[Ag] Chemical compound C(C)#N.[Ag] LOFFIJMYYLJQDG-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 102000053602 DNA Human genes 0.000 description 1
- 230000000970 DNA cross-linking effect Effects 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 235000001453 Glycyrrhiza echinata Nutrition 0.000 description 1
- 244000303040 Glycyrrhiza glabra Species 0.000 description 1
- 235000006200 Glycyrrhiza glabra Nutrition 0.000 description 1
- 235000017382 Glycyrrhiza lepidota Nutrition 0.000 description 1
- 102000006947 Histones Human genes 0.000 description 1
- 108010033040 Histones Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 235000019687 Lamb Nutrition 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 206010033122 Ovarian atrophy Diseases 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 240000006394 Sorghum bicolor Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 101100073357 Streptomyces halstedii sch2 gene Proteins 0.000 description 1
- 235000009430 Thespesia populnea Nutrition 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 210000000601 blood cell Anatomy 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
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 229960002092 busulfan Drugs 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical class CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 210000003679 cervix uteri Anatomy 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 150000001934 cyclohexanes Chemical class 0.000 description 1
- 150000005690 diesters Chemical group 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- UZZWBUYVTBPQIV-UHFFFAOYSA-N dme dimethoxyethane Chemical compound COCCOC.COCCOC UZZWBUYVTBPQIV-UHFFFAOYSA-N 0.000 description 1
- 238000007905 drug manufacturing Methods 0.000 description 1
- 238000003255 drug test Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- XHYXFOFSQYUYBT-UHFFFAOYSA-N ethane-1,1-disulfonyl chloride Chemical compound ClS(=O)(=O)C(C)S(Cl)(=O)=O XHYXFOFSQYUYBT-UHFFFAOYSA-N 0.000 description 1
- XTEXMYNJEMCTNI-UHFFFAOYSA-N ethene;methane Chemical compound C.C=C XTEXMYNJEMCTNI-UHFFFAOYSA-N 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 244000144993 groups of animals Species 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Chemical group 0.000 description 1
- 239000011630 iodine Chemical group 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 231100000518 lethal Toxicity 0.000 description 1
- 230000001665 lethal effect Effects 0.000 description 1
- 229940010454 licorice Drugs 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 210000005265 lung cell Anatomy 0.000 description 1
- 210000002751 lymph Anatomy 0.000 description 1
- 210000004698 lymphocyte Anatomy 0.000 description 1
- 230000000527 lymphocytic effect Effects 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L magnesium sulphate Substances [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- TWXDDNPPQUTEOV-FVGYRXGTSA-N methamphetamine hydrochloride Chemical compound Cl.CN[C@@H](C)CC1=CC=CC=C1 TWXDDNPPQUTEOV-FVGYRXGTSA-N 0.000 description 1
- BUHPOOSGPYCBQX-UHFFFAOYSA-N methane;dihydrate Chemical compound C.O.O BUHPOOSGPYCBQX-UHFFFAOYSA-N 0.000 description 1
- OPUAWDUYWRUIIL-UHFFFAOYSA-L methanedisulfonate Chemical compound [O-]S(=O)(=O)CS([O-])(=O)=O OPUAWDUYWRUIIL-UHFFFAOYSA-L 0.000 description 1
- OPUAWDUYWRUIIL-UHFFFAOYSA-N methanedisulfonic acid Chemical compound OS(=O)(=O)CS(O)(=O)=O OPUAWDUYWRUIIL-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 229940090009 myleran Drugs 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 238000007344 nucleophilic reaction Methods 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 231100001043 ovarian atrophy Toxicity 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012629 purifying agent Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000013076 target substance Substances 0.000 description 1
- 150000003513 tertiary aromatic amines Chemical class 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
- MEYZYGMYMLNUHJ-UHFFFAOYSA-N tunicamycin Natural products CC(C)CCCCCCCCCC=CC(=O)NC1C(O)C(O)C(CC(O)C2OC(C(O)C2O)N3C=CC(=O)NC3=O)OC1OC4OC(CO)C(O)C(O)C4NC(=O)C MEYZYGMYMLNUHJ-UHFFFAOYSA-N 0.000 description 1
- 239000006200 vaporizer Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/570,786 US4950768A (en) | 1984-01-16 | 1984-01-16 | Cyclic disulfonic ester cross-linking compounds |
| US570,786 | 1984-01-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61501089A true JPS61501089A (ja) | 1986-05-29 |
| JPH0544946B2 JPH0544946B2 (https=) | 1993-07-07 |
Family
ID=24281052
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60500579A Granted JPS61501089A (ja) | 1984-01-16 | 1985-01-14 | 環式ジスルホン酸エステル化合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4950768A (https=) |
| EP (1) | EP0168478B1 (https=) |
| JP (1) | JPS61501089A (https=) |
| CA (1) | CA1246087A (https=) |
| DE (1) | DE3569237D1 (https=) |
| WO (1) | WO1985003075A1 (https=) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005336155A (ja) * | 2004-04-28 | 2005-12-08 | Sumitomo Chemical Co Ltd | 環式ジスルホン酸エステルの製造方法 |
| JP2006188449A (ja) * | 2005-01-05 | 2006-07-20 | Sumitomo Chemical Co Ltd | 環式ジスルホン酸エステルの製造方法 |
| JP2006206515A (ja) * | 2005-01-28 | 2006-08-10 | Nec Corp | メチレンジスルホニルクロライド及びその誘導体の製造方法 |
| WO2007125736A1 (ja) * | 2006-04-26 | 2007-11-08 | Sumitomo Seika Chemicals Co., Ltd. | メチレンジスルホネート化合物の製造方法 |
| WO2007148597A1 (ja) | 2006-06-19 | 2007-12-27 | Wako Pure Chemical Industries, Ltd. | 環状ジスルホン酸エステルの製造方法 |
| JP2010184926A (ja) * | 1997-11-10 | 2010-08-26 | Memorial Sloan-Kettering Cancer Center | 三酸化ヒ素製剤の製造方法および三酸化ヒ素またはメラルソプロールを使用する癌の治療方法 |
| JP2010219011A (ja) * | 2009-03-19 | 2010-09-30 | Nec Energy Devices Ltd | 非水電解液およびそれを用いた非水電解液二次電池 |
| WO2012026266A1 (ja) | 2010-08-25 | 2012-03-01 | 住友精化株式会社 | メチレンジスルホネート化合物の製造方法 |
| JP2012131724A (ja) * | 2010-12-21 | 2012-07-12 | Central Glass Co Ltd | 環状ジスルホン酸エステル化合物の製造方法 |
| WO2021015220A1 (ja) | 2019-07-23 | 2021-01-28 | 住友精化株式会社 | 環状ジスルホン酸エステル化合物の製造方法 |
| KR20220041092A (ko) | 2019-07-23 | 2022-03-31 | 스미토모 세이카 가부시키가이샤 | 메틸렌디설포네이트 화합물의 제조 방법 |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5849482A (en) * | 1988-09-28 | 1998-12-15 | Epoch Pharmaceuticals, Inc. | Crosslinking oligonucleotides |
| USRE38416E1 (en) | 1988-09-28 | 2004-02-03 | Epoch Biosciences, Inc. | Cross-linking oligonucleotides |
| US5824796A (en) * | 1988-09-28 | 1998-10-20 | Epoch Pharmaceuticals, Inc. | Cross-linking oligonucleotides |
| EP0472648A4 (en) * | 1989-05-18 | 1992-09-16 | Microprobe Corporation | Crosslinking oligonucleotides |
| US6136601A (en) * | 1991-08-21 | 2000-10-24 | Epoch Pharmaceuticals, Inc. | Targeted mutagenesis in living cells using modified oligonucleotides |
| JP4033074B2 (ja) | 2002-08-29 | 2008-01-16 | 日本電気株式会社 | 二次電池用電解液およびそれを用いた二次電池 |
| WO2005029613A1 (ja) | 2003-09-16 | 2005-03-31 | Nec Corporation | 非水電解液二次電池 |
| JP4725728B2 (ja) * | 2003-12-15 | 2011-07-13 | 日本電気株式会社 | 二次電池 |
| US8445144B2 (en) | 2003-12-15 | 2013-05-21 | Nec Corporation | Additive for an electrolyte solution for an electrochemical device |
| CN101511782B (zh) | 2006-09-12 | 2013-08-07 | 和光纯药工业株式会社 | 磺酸酯的制造方法 |
| US8124793B2 (en) * | 2007-11-27 | 2012-02-28 | Gail Marie Cronyn, legal representative | Derivatives of ethylene methanedisulfonate as cancer chemotherapeutic agents |
| JP5169400B2 (ja) | 2008-04-07 | 2013-03-27 | Ｎｅｃエナジーデバイス株式会社 | 非水電解液およびそれを用いた非水電解液二次電池 |
| JP5408702B2 (ja) | 2009-01-23 | 2014-02-05 | Ｎｅｃエナジーデバイス株式会社 | リチウムイオン電池 |
| US20120115037A1 (en) | 2009-07-09 | 2012-05-10 | Dai-Ichi Kogyo Seiyaku Co., Ltd. | Polymer gel electrolyte and polymer secondary battery using same |
| JPWO2011096572A1 (ja) | 2010-02-08 | 2013-06-13 | Ｎｅｃエナジーデバイス株式会社 | 非水電解液二次電池 |
| WO2011099580A1 (ja) | 2010-02-10 | 2011-08-18 | Ｎｅｃエナジーデバイス株式会社 | 非水系電解液およびそれを備えるリチウムイオン二次電池 |
| CN112574167B (zh) * | 2020-12-07 | 2021-11-09 | 烟台海川化学制品有限公司 | 一种甲烷二磺酸亚甲酯的制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB700677A (en) * | 1950-05-09 | 1953-12-09 | Wellcome Found | Improvements in or relating to aliphatic sulphonic acid esters of therapeutic value |
| AT210874B (de) * | 1959-02-13 | 1960-08-25 | Leuna Werke Veb | Verfahren zur Herstellung von neuen Polysulfosäureestern |
| DE1124032B (de) * | 1960-06-25 | 1962-02-22 | Basf Ag | Verfahren zur Herstellung von Salzen der Halbester der AEthandisulfonsaeure |
| DE1277247B (de) * | 1965-12-08 | 1968-09-12 | Basf Ag | Verfahren zur Herstellung von Vinylsulfonsaeurealkylestern |
| DE3004692A1 (de) * | 1980-02-08 | 1981-08-13 | Agfa-Gevaert Ag, 5090 Leverkusen | Hydroxyalkansulfonsaeure-sulfoalkylester |
-
1984
- 1984-01-16 US US06/570,786 patent/US4950768A/en not_active Expired - Lifetime
-
1985
- 1985-01-14 EP EP85900874A patent/EP0168478B1/en not_active Expired
- 1985-01-14 DE DE8585900874T patent/DE3569237D1/de not_active Expired
- 1985-01-14 WO PCT/US1985/000057 patent/WO1985003075A1/en not_active Ceased
- 1985-01-14 JP JP60500579A patent/JPS61501089A/ja active Granted
- 1985-01-16 CA CA000472222A patent/CA1246087A/en not_active Expired
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7879364B2 (en) | 1997-11-10 | 2011-02-01 | Memorial Sloan-Kettering Cancer Center | Process for producing arsenic trioxide formulations and methods for treating cancer using arsenic trioxide or melarsoprol |
| US8273379B2 (en) | 1997-11-10 | 2012-09-25 | Memorial Sloan-Kettering Cancer Center | Process for producing arsenic trioxide formulations and methods for treating cancer using arsenic trioxide or melarsoprol |
| JP2010184926A (ja) * | 1997-11-10 | 2010-08-26 | Memorial Sloan-Kettering Cancer Center | 三酸化ヒ素製剤の製造方法および三酸化ヒ素またはメラルソプロールを使用する癌の治療方法 |
| JP2005336155A (ja) * | 2004-04-28 | 2005-12-08 | Sumitomo Chemical Co Ltd | 環式ジスルホン酸エステルの製造方法 |
| JP2006188449A (ja) * | 2005-01-05 | 2006-07-20 | Sumitomo Chemical Co Ltd | 環式ジスルホン酸エステルの製造方法 |
| JP2006206515A (ja) * | 2005-01-28 | 2006-08-10 | Nec Corp | メチレンジスルホニルクロライド及びその誘導体の製造方法 |
| KR101355577B1 (ko) * | 2006-04-26 | 2014-01-24 | 스미토모 세이카 가부시키가이샤 | 메틸렌디술포네이트 화합물의 제조방법 |
| JP5247436B2 (ja) * | 2006-04-26 | 2013-07-24 | 住友精化株式会社 | メチレンジスルホネート化合物の製造方法 |
| US7829730B2 (en) | 2006-04-26 | 2010-11-09 | Sumitomo Seika Chemicals Co., Ltd. | Process for production of methylene disulfonate compound |
| WO2007125736A1 (ja) * | 2006-04-26 | 2007-11-08 | Sumitomo Seika Chemicals Co., Ltd. | メチレンジスルホネート化合物の製造方法 |
| US8742136B2 (en) | 2006-06-19 | 2014-06-03 | Wako Pure Chemical Industries, Ltd. | Method for producing cyclic disulfonic acid ester |
| WO2007148597A1 (ja) | 2006-06-19 | 2007-12-27 | Wako Pure Chemical Industries, Ltd. | 環状ジスルホン酸エステルの製造方法 |
| JP5176957B2 (ja) * | 2006-06-19 | 2013-04-03 | 和光純薬工業株式会社 | 環状ジスルホン酸エステルの製造方法 |
| JP2010219011A (ja) * | 2009-03-19 | 2010-09-30 | Nec Energy Devices Ltd | 非水電解液およびそれを用いた非水電解液二次電池 |
| US8501966B2 (en) | 2010-08-25 | 2013-08-06 | Sumitomo Seika Chemicals Co., Ltd. | Method for producing a methylene disulfonate compound |
| WO2012026266A1 (ja) | 2010-08-25 | 2012-03-01 | 住友精化株式会社 | メチレンジスルホネート化合物の製造方法 |
| JP2012131724A (ja) * | 2010-12-21 | 2012-07-12 | Central Glass Co Ltd | 環状ジスルホン酸エステル化合物の製造方法 |
| WO2021015220A1 (ja) | 2019-07-23 | 2021-01-28 | 住友精化株式会社 | 環状ジスルホン酸エステル化合物の製造方法 |
| KR20220035913A (ko) | 2019-07-23 | 2022-03-22 | 스미토모 세이카 가부시키가이샤 | 환상 디설폰산에스테르 화합물의 제조 방법 |
| KR20220041092A (ko) | 2019-07-23 | 2022-03-31 | 스미토모 세이카 가부시키가이샤 | 메틸렌디설포네이트 화합물의 제조 방법 |
| US11802119B2 (en) | 2019-07-23 | 2023-10-31 | Sumitomo Seika Chemicals Co., Ltd. | Method for producing cyclic disulfonic acid ester compound |
| US12129239B2 (en) | 2019-07-23 | 2024-10-29 | Sumitomo Seika Chemicals Co., Ltd. | Method for producing methylene disulfonate compound |
Also Published As
| Publication number | Publication date |
|---|---|
| DE3569237D1 (en) | 1989-05-11 |
| CA1246087A (en) | 1988-12-06 |
| JPH0544946B2 (https=) | 1993-07-07 |
| EP0168478A1 (en) | 1986-01-22 |
| EP0168478A4 (en) | 1986-11-07 |
| US4950768A (en) | 1990-08-21 |
| EP0168478B1 (en) | 1989-04-05 |
| WO1985003075A1 (en) | 1985-07-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS61501089A (ja) | 環式ジスルホン酸エステル化合物 | |
| RU2039064C1 (ru) | Четырехкоординационные комплексы двухвалентной платины | |
| JPS58219177A (ja) | （＋）−シアニダン−３−オ−ル誘導体を含む医薬製剤、置換（＋）−シアニダン−３−オ−ル誘導体及び該誘導体の製造方法 | |
| WO2004063208A1 (en) | New phosphoramidite compounds | |
| CN1030658C (zh) | 十八烷基-[2-(n-甲基哌啶子基)-乙基]-磷酸酯的制备方法 | |
| JPS59190998A (ja) | 新規ビス（２，２−ジメチル−１−アジリジニル）ホスフインアミド類及びその腫瘍阻止組成物 | |
| US3448137A (en) | Method of preparing 4-alkyl-2,2-dimethyl-2-silamorpholines | |
| US3709960A (en) | O-loweralkyl-o-(2-alkoxylcarbonylmethyl)vinyl-monoalkylamido phosphates | |
| US3879411A (en) | Ditetrazolyl-benzodipyrans | |
| US2855426A (en) | O-(cyclohexylphenyl) phosphoroamidothioates | |
| US3075983A (en) | -oconh | |
| EP0190568A1 (de) | Verfahren zur Herstellung von Spiroorthocarbonaten | |
| US3828090A (en) | Alkylsulfonic acid esters of 1,3,2-oxazaphospha-cyclic compounds | |
| US3202712A (en) | 1-cyclohexene-4-bis (omicron-chlorobenzylaminomethyl) and derivatives | |
| JPH0450312B2 (https=) | ||
| US3429923A (en) | Boron-nitrogen compounds and process for the preparation thereof | |
| US3557208A (en) | N-(substituted phenyl) trialkyl phosphine imide | |
| KR940009935B1 (ko) | N-벤조일-c-티오펜옥시이미도일 클로라이드 유도체 및 그 제조방법 | |
| JPS5838436B2 (ja) | １ ２− ジアルキルケトン−グリセリン −３− ホスフアタイド ノ セイホウ | |
| US2848481A (en) | New guanidine compounds, their preparation and use as reagents for picric acid | |
| AT204565B (de) | Verfahren zur Herstellung neuer Phosphorsäure- bzw. Thiophosphorsäure-Derivate | |
| JPH07330783A (ja) | リン酸エステル誘導体の製造方法 | |
| US3737446A (en) | Amino-substituted mercapto compounds and their preparation by the reaction of aminothiosulfuric acids and aziridines | |
| US3759949A (en) | Process of manufacturing organo-phosphorous derivatives | |
| JPH0563476B2 (https=) |