ES2621881T3 - 1,2-Bis-(4,7-dimetil-1,4,7-triazaciclonon-1-il)-etano e intermedio del mismo - Google Patents
1,2-Bis-(4,7-dimetil-1,4,7-triazaciclonon-1-il)-etano e intermedio del mismo Download PDFInfo
- Publication number
- ES2621881T3 ES2621881T3 ES11803066.7T ES11803066T ES2621881T3 ES 2621881 T3 ES2621881 T3 ES 2621881T3 ES 11803066 T ES11803066 T ES 11803066T ES 2621881 T3 ES2621881 T3 ES 2621881T3
- Authority
- ES
- Spain
- Prior art keywords
- compound
- formula
- acid
- water
- tacn
- 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.)
- Active
Links
- JJICBMPGGOIYHR-UHFFFAOYSA-N 1-[2-(4,7-dimethyl-1,4,7-triazonan-1-yl)ethyl]-4,7-dimethyl-1,4,7-triazonane Chemical compound C1CN(C)CCN(C)CCN1CCN1CCN(C)CCN(C)CC1 JJICBMPGGOIYHR-UHFFFAOYSA-N 0.000 title claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 55
- 150000001875 compounds Chemical class 0.000 claims abstract description 48
- 238000000034 method Methods 0.000 claims abstract description 46
- 150000003839 salts Chemical class 0.000 claims abstract description 25
- 230000002378 acidificating effect Effects 0.000 claims abstract description 18
- 125000005228 aryl sulfonate group Chemical group 0.000 claims abstract description 18
- 125000006239 protecting group Chemical group 0.000 claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 claims abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 109
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 52
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 40
- 238000006243 chemical reaction Methods 0.000 claims description 39
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 23
- 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 20
- 239000002253 acid Substances 0.000 claims description 15
- 235000019253 formic acid Nutrition 0.000 claims description 12
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 11
- DSJWOERHCVJUFY-UHFFFAOYSA-N 1-[2-(1,4,7-triazonan-1-yl)ethyl]-1,4,7-triazonane Chemical compound C1CNCCNCCN1CCN1CCNCCNCC1 DSJWOERHCVJUFY-UHFFFAOYSA-N 0.000 claims description 8
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 claims description 8
- 150000008065 acid anhydrides Chemical class 0.000 claims description 8
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 claims description 7
- 229940077388 benzenesulfonate Drugs 0.000 claims description 7
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 5
- 229940092714 benzenesulfonic acid Drugs 0.000 claims description 5
- 150000008064 anhydrides Chemical class 0.000 claims description 3
- YNUCBHYNXQGNQR-UHFFFAOYSA-N 1,4-bis-(4-methylphenyl)sulfonyl-1,4,7-triazonane Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N1CCN(S(=O)(=O)C=2C=CC(C)=CC=2)CCNCC1 YNUCBHYNXQGNQR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 239000012429 reaction media Substances 0.000 claims description 2
- VEIZBFQQWHDSEO-UHFFFAOYSA-N 2-sulfonyl-1,4,7-triazonane Chemical compound S(=O)(=O)=C1NCCNCCNC1 VEIZBFQQWHDSEO-UHFFFAOYSA-N 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 63
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 62
- 239000000203 mixture Substances 0.000 description 43
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 27
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 26
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 26
- 239000000047 product Substances 0.000 description 23
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 20
- 238000002360 preparation method Methods 0.000 description 20
- 239000002904 solvent Substances 0.000 description 20
- 238000004458 analytical method Methods 0.000 description 17
- 238000003756 stirring Methods 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- 239000003921 oil Substances 0.000 description 15
- 239000007787 solid Substances 0.000 description 15
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 14
- 239000003446 ligand Substances 0.000 description 14
- 238000004809 thin layer chromatography Methods 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 11
- 238000010992 reflux Methods 0.000 description 11
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 10
- 229910000029 sodium carbonate Inorganic materials 0.000 description 10
- 235000017550 sodium carbonate Nutrition 0.000 description 10
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 238000001816 cooling Methods 0.000 description 9
- -1 (4,7-ditosyl-1,4,7-triazacyclonon-1-yl) -ethane Chemical compound 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- ITWBWJFEJCHKSN-UHFFFAOYSA-N 1,4,7-triazonane Chemical compound C1CNCCNCCN1 ITWBWJFEJCHKSN-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 6
- 238000007069 methylation reaction Methods 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- 235000011149 sulphuric acid Nutrition 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 238000005881 detosylation reaction Methods 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000012065 filter cake Substances 0.000 description 5
- 235000019260 propionic acid Nutrition 0.000 description 5
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 150000003335 secondary amines Chemical class 0.000 description 5
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 4
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 229910052748 manganese Inorganic materials 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- 230000011987 methylation Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 238000006824 Eschweiler-Clarke methylation reaction Methods 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 230000000536 complexating effect Effects 0.000 description 3
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 3
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 3
- 150000002696 manganese Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 238000004704 ultra performance liquid chromatography Methods 0.000 description 3
- 238000004457 water analysis Methods 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000004391 aryl sulfonyl group Chemical group 0.000 description 2
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000010668 complexation reaction Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 238000010511 deprotection reaction Methods 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000005580 one pot reaction Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 1
- JNVXRQOSRUDXDY-UHFFFAOYSA-N 1,1-diiodoethane Chemical compound CC(I)I JNVXRQOSRUDXDY-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- WLDGDTPNAKWAIR-UHFFFAOYSA-N 1,4,7-trimethyl-1,4,7-triazonane Chemical compound CN1CCN(C)CCN(C)CC1 WLDGDTPNAKWAIR-UHFFFAOYSA-N 0.000 description 1
- BLZOXONTWBENEK-UHFFFAOYSA-N 1,4,7-tris-(4-methylphenyl)sulfonyl-1,4,7-triazonane Chemical compound C1=CC(C)=CC=C1S(=O)(=O)N1CCN(S(=O)(=O)C=2C=CC(C)=CC=2)CCN(S(=O)(=O)C=2C=CC(C)=CC=2)CC1 BLZOXONTWBENEK-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- BPUTWIXLCVEAMX-UHFFFAOYSA-N 1-[2-[4,7-bis-(4-methylphenyl)sulfonyl-1,4,7-triazonan-1-yl]ethyl]-4,7-bis-(4-methylphenyl)sulfonyl-1,4,7-triazonane Chemical group C1=CC(C)=CC=C1S(=O)(=O)N1CCN(S(=O)(=O)C=2C=CC(C)=CC=2)CCN(CCN2CCN(CCN(CC2)S(=O)(=O)C=2C=CC(C)=CC=2)S(=O)(=O)C=2C=CC(C)=CC=2)CC1 BPUTWIXLCVEAMX-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- ZMZINYUKVRMNTG-UHFFFAOYSA-N acetic acid;formic acid Chemical compound OC=O.CC(O)=O ZMZINYUKVRMNTG-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000012296 anti-solvent Substances 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 238000004380 ashing Methods 0.000 description 1
- ASECQKAOOLEMTR-UHFFFAOYSA-N benzene;4-methylbenzenesulfonic acid Chemical compound C1=CC=CC=C1.CC1=CC=C(S(O)(=O)=O)C=C1 ASECQKAOOLEMTR-UHFFFAOYSA-N 0.000 description 1
- BKUYVGOACRJHQO-UHFFFAOYSA-N benzenesulfonic acid;sulfuric acid Chemical compound OS(O)(=O)=O.OS(=O)(=O)C1=CC=CC=C1 BKUYVGOACRJHQO-UHFFFAOYSA-N 0.000 description 1
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- 239000004914 cyclooctane Substances 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000013461 intermediate chemical Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000000622 liquid--liquid extraction Methods 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000012521 purified sample Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000006268 reductive amination reaction Methods 0.000 description 1
- 238000006485 reductive methylation reaction Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000006248 tosyl amino group Chemical group [H]N(*)S(=O)(=O)C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- 125000005490 tosylate group Chemical group 0.000 description 1
- 238000002371 ultraviolet--visible spectrum Methods 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D255/00—Heterocyclic compounds containing rings having three nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D249/00 - C07D253/00
- C07D255/02—Heterocyclic compounds containing rings having three nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D249/00 - C07D253/00 not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2010/001007 WO2012003598A1 (en) | 2010-07-06 | 2010-07-06 | Intermediates for the synthesis of 1,2-bis(4,7-dimethyl-1,4,7-triazacyclonon-1-yl)-ethane and preparation method thereof |
| WOPCT/CN2010/001007 | 2010-07-06 | ||
| PCT/CN2010/001008 WO2012003599A1 (en) | 2010-07-06 | 2010-07-06 | Methods for the synthesis of bis (triazacyclononane) ligands |
| WOPCT/CN2010/001008 | 2010-07-06 | ||
| PCT/CN2011/001104 WO2012003712A1 (en) | 2010-07-06 | 2011-07-05 | 1,2-bis-(4,7-dimethyl-1,4,7-triazacyclonon-1-yl)-ethane and intermediate thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2621881T3 true ES2621881T3 (es) | 2017-07-05 |
Family
ID=45440772
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES17151457T Active ES2764203T3 (es) | 2010-07-06 | 2011-07-05 | 1,2-bis-(4,7-dimetil-1,4,7-triazaciclonon-1-il)-etano y producto intermedio para la síntesis del mismo |
| ES11803066.7T Active ES2621881T3 (es) | 2010-07-06 | 2011-07-05 | 1,2-Bis-(4,7-dimetil-1,4,7-triazaciclonon-1-il)-etano e intermedio del mismo |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES17151457T Active ES2764203T3 (es) | 2010-07-06 | 2011-07-05 | 1,2-bis-(4,7-dimetil-1,4,7-triazaciclonon-1-il)-etano y producto intermedio para la síntesis del mismo |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US8907082B2 (enExample) |
| EP (2) | EP2590952B1 (enExample) |
| CN (1) | CN103180302B (enExample) |
| BR (1) | BR112013000236B1 (enExample) |
| CA (2) | CA3052591A1 (enExample) |
| ES (2) | ES2764203T3 (enExample) |
| HU (1) | HUE049652T2 (enExample) |
| IN (1) | IN2013MN00119A (enExample) |
| PL (1) | PL2590952T3 (enExample) |
| PT (1) | PT3176155T (enExample) |
| WO (1) | WO2012003712A1 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2900742C (en) | 2013-02-11 | 2021-08-24 | Chemsenti Limited | Drier for alkyd-based coating |
| WO2014122432A1 (en) | 2013-02-11 | 2014-08-14 | Chemsenti Limited | Oxidatively curable coating composition |
| CN104529922A (zh) * | 2014-12-12 | 2015-04-22 | 沈阳感光化工研究院有限公司 | 一种1,4,7-三氮杂环壬烷盐酸盐的制备方法 |
| CN113277990A (zh) * | 2021-06-22 | 2021-08-20 | 仪征市海帆化工有限公司 | 一种1,4-双(对甲苯磺酰基)三氮环壬烷的合成方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60130551A (ja) | 1983-12-16 | 1985-07-12 | Kao Corp | 第３級アミンの製造方法 |
| US5362476A (en) * | 1984-10-18 | 1994-11-08 | Board Of Regents, The University Of Texas System | Alkyl phosphonate polyazamacrocyclic cheates for MRI |
| US5105013A (en) | 1988-12-19 | 1992-04-14 | The Dow Chemical Company | Method for the reductive methylation of primary amines |
| WO1990007261A2 (en) * | 1988-12-22 | 1990-07-12 | The Dow Chemical Company | Process for preparing mono-n-alkylated polyazamacrocycles |
| EP0553954A3 (en) | 1992-01-27 | 1993-11-10 | Texaco Chemical | Preparation of tetramethyldiamino-polyoxyethylenes |
| US5284944A (en) * | 1992-06-30 | 1994-02-08 | Lever Brothers Company, Division Of Conopco, Inc. | Improved synthesis of 1,4,7-triazacyclononane |
| CN1384837A (zh) * | 1999-09-01 | 2002-12-11 | 荷兰联合利华有限公司 | 用于催化漂白底物的配体和配合物 |
| GB0004852D0 (en) * | 2000-02-29 | 2000-04-19 | Unilever Plc | Ligand and complex for catalytically bleaching a substrate |
| US20050112066A1 (en) | 2003-11-26 | 2005-05-26 | Concat Lp, A California Limited Partnership | Complexes of cyclic polyaza chelators with cations of alkaline earth metals for enhanced biological activity |
| MX2007014898A (es) | 2005-05-27 | 2008-01-28 | Unilever Nv | Proceso de blanqueo. |
| GB201102037D0 (en) | 2011-02-07 | 2011-03-23 | Multi Sense Technologies Ltd | Microfluidics based assay device |
-
2011
- 2011-06-05 BR BR112013000236-0A patent/BR112013000236B1/pt not_active IP Right Cessation
- 2011-07-05 EP EP11803066.7A patent/EP2590952B1/en active Active
- 2011-07-05 PT PT171514573T patent/PT3176155T/pt unknown
- 2011-07-05 IN IN119MUN2013 patent/IN2013MN00119A/en unknown
- 2011-07-05 US US13/808,565 patent/US8907082B2/en active Active
- 2011-07-05 CA CA3052591A patent/CA3052591A1/en not_active Abandoned
- 2011-07-05 ES ES17151457T patent/ES2764203T3/es active Active
- 2011-07-05 CA CA2804475A patent/CA2804475C/en not_active Expired - Fee Related
- 2011-07-05 WO PCT/CN2011/001104 patent/WO2012003712A1/en not_active Ceased
- 2011-07-05 HU HUE17151457A patent/HUE049652T2/hu unknown
- 2011-07-05 EP EP17151457.3A patent/EP3176155B1/en active Active
- 2011-07-05 CN CN201180042920.4A patent/CN103180302B/zh active Active
- 2011-07-05 ES ES11803066.7T patent/ES2621881T3/es active Active
- 2011-07-05 PL PL11803066T patent/PL2590952T3/pl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP3176155A1 (en) | 2017-06-07 |
| EP2590952B1 (en) | 2017-01-18 |
| CA2804475A1 (en) | 2012-01-12 |
| US8907082B2 (en) | 2014-12-09 |
| EP2590952A1 (en) | 2013-05-15 |
| IN2013MN00119A (enExample) | 2015-05-29 |
| EP2590952A4 (en) | 2014-03-05 |
| EP3176155B1 (en) | 2019-09-25 |
| CN103180302A (zh) | 2013-06-26 |
| BR112013000236A2 (pt) | 2016-05-17 |
| ES2764203T3 (es) | 2020-06-02 |
| WO2012003712A1 (en) | 2012-01-12 |
| CA2804475C (en) | 2019-10-15 |
| PT3176155T (pt) | 2020-01-10 |
| US20130261297A1 (en) | 2013-10-03 |
| CA3052591A1 (en) | 2012-01-12 |
| PL2590952T3 (pl) | 2017-09-29 |
| CN103180302B (zh) | 2016-08-03 |
| BR112013000236B1 (pt) | 2018-11-13 |
| HUE049652T2 (hu) | 2020-10-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP7318871B2 (ja) | アンモニアの製造方法、モリブデン錯体及びベンゾイミダゾール化合物 | |
| ES2621881T3 (es) | 1,2-Bis-(4,7-dimetil-1,4,7-triazaciclonon-1-il)-etano e intermedio del mismo | |
| JP2013216696A (ja) | 触媒性水素転移反応を使用する新規なオピエート還元 | |
| EP2036899B1 (en) | Method for producing cyclic disulfonic acid ester | |
| CN111556863B (zh) | 制备双环胍及其衍生物的方法 | |
| TW202219024A (zh) | 鹼土金屬甲酸鹽之製造方法 | |
| KR20170034077A (ko) | 고리형 카보네이트 제조용 금속 촉매, 이를 이용한 고리형 카보네이트의 제조방법 및 제조된 고리형 카보네이트의 용도 | |
| JP2004517871A (ja) | ２−（２−ヒドロキシフェニル）−２ｈ−ベンゾトリアゾールの製造方法 | |
| KR101839877B1 (ko) | 신규한 유기촉매 및 이를 이용한 알킬렌 카보네이트의 제조방법 | |
| FI91751B (fi) | Menetelmä oksatsolidiinifenolieetterin valmistamiseksi | |
| JP5165369B2 (ja) | マイクロ波を利用したグリコールウリル及びククルビツリルの製造方法 | |
| JP6816274B2 (ja) | （ｓ）−ｎ１−（２−アミノエチル）−３−（４−アルコキシフェニル）プロパン−１，２−ジアミン三塩酸塩の製造方法 | |
| Cubanski et al. | Low symmetry pyrazole-based tripodal tetraamine ligands: metal complexes and ligand decomposition reactions | |
| ES2399245T3 (es) | Procedimiento para producir bepromolina | |
| CN104774183B (zh) | 一种甲酰基瑞舒伐汀钙中间体的制备方法 | |
| WO2012003598A1 (en) | Intermediates for the synthesis of 1,2-bis(4,7-dimethyl-1,4,7-triazacyclonon-1-yl)-ethane and preparation method thereof | |
| CN113214256A (zh) | 1,7-二氮杂螺[3.5]壬烷-7-甲酸叔丁基酯的合成方法 | |
| KR100726890B1 (ko) | 금속 킬레이션용 티오펜 배위자의 합성방법 | |
| ITMI20110343A1 (it) | Processo per la sintesi enantioselettiva di landiolol | |
| CN117946052A (zh) | 3,3'-羰基双(7-二乙氨基香豆素)化合物的制备方法 | |
| ES2348770T3 (es) | Sintesis directa de sales cuaternarias. | |
| SU554811A3 (ru) | Способ получени метилсульфонильных производных | |
| CN118221612A (zh) | 一种l-[2-（2,4-二甲基苯硫基）-苯基]哌嗪氢卤酸盐的制备方法 | |
| WO2012003599A1 (en) | Methods for the synthesis of bis (triazacyclononane) ligands | |
| KR20050094528A (ko) | 키랄 살렌 망간촉매의 제조방법 |