JP2017128559A - ルテニウム錯体の製造方法 - Google Patents
ルテニウム錯体の製造方法 Download PDFInfo
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- JP2017128559A JP2017128559A JP2016091677A JP2016091677A JP2017128559A JP 2017128559 A JP2017128559 A JP 2017128559A JP 2016091677 A JP2016091677 A JP 2016091677A JP 2016091677 A JP2016091677 A JP 2016091677A JP 2017128559 A JP2017128559 A JP 2017128559A
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- 239000012327 Ruthenium complex Substances 0.000 title claims abstract description 37
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims abstract description 92
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims abstract description 34
- 125000003118 aryl group Chemical group 0.000 claims abstract description 33
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 21
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims abstract description 18
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 38
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 33
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 32
- 238000006243 chemical reaction Methods 0.000 claims description 20
- 239000003446 ligand Substances 0.000 claims description 19
- 229910052717 sulfur Inorganic materials 0.000 claims description 16
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 125000004434 sulfur atom Chemical group 0.000 claims description 6
- 101100240516 Caenorhabditis elegans nhr-10 gene Proteins 0.000 claims description 3
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 1
- -1 phosphine diamine Chemical class 0.000 abstract description 201
- DHCWLIOIJZJFJE-UHFFFAOYSA-L dichlororuthenium Chemical compound Cl[Ru]Cl DHCWLIOIJZJFJE-UHFFFAOYSA-L 0.000 abstract description 11
- 150000001875 compounds Chemical class 0.000 abstract description 9
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 abstract description 3
- 150000004985 diamines Chemical class 0.000 abstract description 3
- 229910052707 ruthenium Inorganic materials 0.000 abstract description 3
- YBCAZPLXEGKKFM-UHFFFAOYSA-K ruthenium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Ru+3] YBCAZPLXEGKKFM-UHFFFAOYSA-K 0.000 abstract description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 2
- SBUXRMKDJWEXRL-ROUUACIJSA-N cis-body Chemical compound O=C([C@H]1N(C2=O)[C@H](C3=C(C4=CC=CC=C4N3)C1)CC)N2C1=CC=C(F)C=C1 SBUXRMKDJWEXRL-ROUUACIJSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 description 29
- BCJVBDBJSMFBRW-UHFFFAOYSA-N 4-diphenylphosphanylbutyl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CCCCP(C=1C=CC=CC=1)C1=CC=CC=C1 BCJVBDBJSMFBRW-UHFFFAOYSA-N 0.000 description 24
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- 239000002904 solvent Substances 0.000 description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 16
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 239000013078 crystal Substances 0.000 description 12
- 239000003960 organic solvent Substances 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 125000001424 substituent group Chemical group 0.000 description 10
- MPBCUCGKHDEUDD-UHFFFAOYSA-N (5-methylpyrazin-2-yl)methanamine Chemical compound CC1=CN=C(CN)C=N1 MPBCUCGKHDEUDD-UHFFFAOYSA-N 0.000 description 9
- WOXFMYVTSLAQMO-UHFFFAOYSA-N 2-Pyridinemethanamine Chemical compound NCC1=CC=CC=N1 WOXFMYVTSLAQMO-UHFFFAOYSA-N 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- 150000001721 carbon Chemical group 0.000 description 9
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
- 229910052801 chlorine Inorganic materials 0.000 description 7
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 4
- 125000006651 (C3-C20) cycloalkyl group Chemical group 0.000 description 4
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 4
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 description 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- VURFVHCLMJOLKN-UHFFFAOYSA-N diphosphane Chemical compound PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 description 4
- OBNCKNCVKJNDBV-UHFFFAOYSA-N ethyl butyrate Chemical compound CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 125000004404 heteroalkyl group Chemical group 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical class NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- 241001482237 Pica Species 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- XLJMAIOERFSOGZ-UHFFFAOYSA-N cyanic acid Chemical compound OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 125000001072 heteroaryl group Chemical group 0.000 description 3
- 125000000592 heterocycloalkyl group Chemical group 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 125000006606 n-butoxy group Chemical group 0.000 description 3
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- HQIBSDCOMQYSPF-UHFFFAOYSA-N pyrazin-2-ylmethanamine Chemical compound NCC1=CN=CC=N1 HQIBSDCOMQYSPF-UHFFFAOYSA-N 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 125000006413 ring segment Chemical group 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 3
- GFQZSGGPNZDNBC-UHFFFAOYSA-N (1-methylbenzimidazol-2-yl)methanamine Chemical compound C1=CC=C2N(C)C(CN)=NC2=C1 GFQZSGGPNZDNBC-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- IOPQYDKQISFMJI-UHFFFAOYSA-N [1-[2-bis(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C1=CC(C)=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 IOPQYDKQISFMJI-UHFFFAOYSA-N 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 125000003282 alkyl amino group Chemical group 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical compound C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 229940117389 dichlorobenzene Drugs 0.000 description 2
- GPAYUJZHTULNBE-UHFFFAOYSA-N diphenylphosphine Chemical compound C=1C=CC=CC=1PC1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-N 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 125000004438 haloalkoxy group Chemical group 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- YUWFEBAXEOLKSG-UHFFFAOYSA-N hexamethylbenzene Chemical compound CC1=C(C)C(C)=C(C)C(C)=C1C YUWFEBAXEOLKSG-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000005453 ketone based solvent Substances 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001298 n-hexoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- MDAHANCDXSBKPT-UHFFFAOYSA-N (1-cyclohexyl-2-diphenylphosphanylethyl)-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CC(P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1CCCCC1 MDAHANCDXSBKPT-UHFFFAOYSA-N 0.000 description 1
- QKZWXPLBVCKXNQ-UHFFFAOYSA-N (2-methoxyphenyl)-[2-[(2-methoxyphenyl)-phenylphosphanyl]ethyl]-phenylphosphane Chemical compound COC1=CC=CC=C1P(C=1C=CC=CC=1)CCP(C=1C(=CC=CC=1)OC)C1=CC=CC=C1 QKZWXPLBVCKXNQ-UHFFFAOYSA-N 0.000 description 1
- VMIPGHCGBQOEOQ-UHFFFAOYSA-N (3,5-dimethylphenyl)-[1-[2-(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]phosphane Chemical group CC1=CC(C)=CC(PC=2C(=C3C=CC=CC3=CC=2)C=2C3=CC=CC=C3C=CC=2PC=2C=C(C)C=C(C)C=2)=C1 VMIPGHCGBQOEOQ-UHFFFAOYSA-N 0.000 description 1
- CCMBUTYBPHGIQH-UHFFFAOYSA-N (4-methylphenyl)-[1-[2-(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]phosphane Chemical group C1=CC(C)=CC=C1PC1=CC=C(C=CC=C2)C2=C1C(C1=CC=CC=C1C=C1)=C1PC1=CC=C(C)C=C1 CCMBUTYBPHGIQH-UHFFFAOYSA-N 0.000 description 1
- FAPIYUMKTQPQTR-UHFFFAOYSA-N (4-propan-2-ylphenyl)-[1-[2-(4-propan-2-ylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]phosphane Chemical group C1=CC(C(C)C)=CC=C1PC1=CC=C(C=CC=C2)C2=C1C(C1=CC=CC=C1C=C1)=C1PC1=CC=C(C(C)C)C=C1 FAPIYUMKTQPQTR-UHFFFAOYSA-N 0.000 description 1
- MADOPTWMOUJWBZ-UHFFFAOYSA-N (4-tert-butylphenyl)-[1-[2-(4-tert-butylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]phosphane Chemical group C1=CC(C(C)(C)C)=CC=C1PC1=CC=C(C=CC=C2)C2=C1C(C1=CC=CC=C1C=C1)=C1PC1=CC=C(C(C)(C)C)C=C1 MADOPTWMOUJWBZ-UHFFFAOYSA-N 0.000 description 1
- MKMPVMGXVLFXDN-UHFFFAOYSA-N (5-methylpiperazin-2-yl)methanamine Chemical compound CC1CNC(CN)CN1 MKMPVMGXVLFXDN-UHFFFAOYSA-N 0.000 description 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 description 1
- 125000004814 1,1-dimethylethylene group Chemical group [H]C([H])([H])C([*:1])(C([H])([H])[H])C([H])([H])[*:2] 0.000 description 1
- 125000005656 1,2-cyclobutylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C1([H])[*:2] 0.000 description 1
- 125000005657 1,3-cyclobutylene group Chemical group [H]C1([H])C([H])([*:1])C([H])([H])C1([H])[*:2] 0.000 description 1
- WGOBPPNNYVSJTE-UHFFFAOYSA-N 1-diphenylphosphanylpropan-2-yl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)CP(C=1C=CC=CC=1)C1=CC=CC=C1 WGOBPPNNYVSJTE-UHFFFAOYSA-N 0.000 description 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
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- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- OOLUVSIJOMLOCB-UHFFFAOYSA-N 1633-22-3 Chemical group C1CC(C=C2)=CC=C2CCC2=CC=C1C=C2 OOLUVSIJOMLOCB-UHFFFAOYSA-N 0.000 description 1
- 125000004797 2,2,2-trichloroethoxy group Chemical group ClC(CO*)(Cl)Cl 0.000 description 1
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 description 1
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- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
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- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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- 238000002955 isolation Methods 0.000 description 1
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- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 125000004312 morpholin-2-yl group Chemical group [H]N1C([H])([H])C([H])([H])OC([H])(*)C1([H])[H] 0.000 description 1
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- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
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- LBRFRRGENNWKKV-UHFFFAOYSA-N naphthalen-2-yl-[1-(2-naphthalen-2-ylphosphanylnaphthalen-1-yl)naphthalen-2-yl]phosphane Chemical group C1=CC2=CC=CC=C2C(C2=C3C=CC=CC3=CC=C2PC=2C=C3C=CC=CC3=CC=2)=C1PC1=CC=C(C=CC=C2)C2=C1 LBRFRRGENNWKKV-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
a)一般式PR1R2R3の単座配位子のホスフィンであって、R1、R2、及びR3が同一又は異なって、脂肪族又は芳香族であるものであり、
b)式PR’2(CH2)xPR’’2の二座配位子のホスフィンであって、xが2、3、又は4であり、R’、R’’が同一または異なって、脂肪族又は芳香族であるものであり、
c)光学活性を有するジホスフィンである
から選択されたリガンドであり、mは、リガンドLが上記b)又はc)から選択される場合には1であり、上記a)から選択される場合には、Lが同一又は異なって、2であり、
L’は下記式(II)
で表される2−アミノメチルピリジンの二座配位子のリガンドである。)
で表されるルテニウム錯体は、ケトン類をアルコール類へ水素還元する触媒として有用であることが知られている。また、2−アミノメチルピリジン二座配位子の配位する位置により、シス体、トランス体の立体異性体が存在する。
その製造方法は、例えば、公知の方法(Inorg. Chem., 1984,23,726)の方法によって得られたRuCl2[PPh2(CH2)4PPh2](PPh3)を出発物質として、トルエン中、2−(アミノメチル)ピリジンと還流化20時間反応させることにより、シス−RuCl2[PPh2(CH2)4PPh2][2−(H2NCH2)C5NH4]を収率76%で得られることが知られている。(特許文献1を参照)
本発明は、収率よく、しかもシス体を選択性よく得られるホスフィンジアミンルテニウム錯体の製造方法を提供することを目的とする。
前記A環は、下記式(2)
又は下記式(3)
下記式(4)
で表されるルテニウム錯体と、R1R2R3P及びR4R5R6P(この式中、R1〜R6は、前記式(1)中のR1〜R6と同じ意味を表す。)と、をジメチルホルムアミド(dmf)中で反応させて、
下記式(5)
C3−20シクロアルキル基とは、3から20個の炭素原子、好ましくは3から14個、さらに好ましくは3から10個(特に、3、4、5、6、または7個)の炭素原子を有する骨格を形成する1個以上の環(好ましくは1または2個の環)を有する、飽和または部分的に不飽和の環式の基(例えば、シクロアルケニル)を示す。
R2R3PWPR5R6 (7)
(式(7)中、R2、R3、R5及びR6は、前記式(1)中のR2、R3、R5及びR6と同じ意味を表し、Wは、無置換又は置換基を有する結合鎖を表す。)で表される2座配位のホスフィンとなる。
式(2)中、R7及びR8は、それぞれ独立に、水素原子、脂肪族基、または芳香族基を表し、具体的には、R1〜R6で例示した官能基と同じ官能基を例示することができる。
炭素数1〜4の二価の脂肪族基として具体的には、メチレン基、メチルメチレン基、エチレン基、1、3−プロピレン基、1、2−プロピレン基、1、4−ブチレン基、1、3−ブチレン基、2、4−ブチレン基、1,1−ジメチルエチレン基等の直鎖状または分岐したアルキレン基、シクロプロピレン基、1−メチルシクロプロピレン基、1、3−シクロブチレン基、1、2−シクロブチレン基等のシクロアルキレン等を例示することができる。
Y2は、NHR10(R10は、水素原子、アルキル基、又はアリール基を表す。)またはSHを表す。R10として、具体的には、R9で例示した官能基と同じ官能基を例示することができる。
これらの化合物は、公知の方法または、公知の方法を応用して製造することができる。たとえば、2−アミノメチル−5−メチルピラジンの場合、対応する5−メチルピラジン2−カルボニトリルを還元することにより製造することができる。還元方法は、特に制限されないが、具体的には、特開平3−137373号公報に記載されているような金属触媒存在下、水素添加する方法等を例示することができる。その際、副生する2−アミノメチル−5−メチルピペラジンは、2−アミノメチル−5−メチルピラジンと分離精製することなく、混合物として使用することができる。
有機溶媒中で反応を行う場合、用いる有機溶媒としては、特に制限されず、例えば、テトラヒドロフラン、ジオキサン等のエーテル系溶媒、クロロホルム、四塩化炭素、モノクロロベンゼン、ジクロロベンゼン等の塩素系溶媒、ベンゼン、トルエン、キシレン等の芳香族炭化水素系溶媒、ヘキサン、テトラリン等の脂肪族系炭化水素系溶媒、アセトン、シクロヘキサノン、メチルイソブチルケトン等のケトン系溶媒、酢酸エチル、酢酸ブチル、ブタン酸エチル等のエステル系溶媒、ジメチルスルホキシド、ジメチルホルムアミド、ジメチルアセトアミド等を例示することができる。
反応時間は、反応させる基質、反応試剤、反応温度によって異なるが、5分〜120分程度が好ましい。
(1)ルテニウム錯体(4)、ジメチルホルムアミド及びホスフィンを混合して、加熱する方法、
(2)ルテニウム錯体(4)及びジメチルホルムアミドの混合物を加熱し、ホスフィン又はそのジメチルホルムアミド溶液を添加する方法、
(3)ホスフィン及びジメチルホルムアミドの混合物を加熱し、ルテニウム錯体(4)又はそのジメチルホルムアミド溶液を添加する方法、
(4)上記(1)〜(3)のいずれかの方法を有機溶媒中で行う方法
等、いずれの方法でも行うことができる。
得られたホスフィン−dmf−ルテニウム錯体は、さらに、式(5)で表される窒素原子含有配位子(以下、「窒素原子含有配位子(5)」という)と反応させることにより、目的とする下記式(1)で表される錯体(以下「ルテニウム錯体(1)」という)を得ることができる。
用いる反応溶媒は、特に制限されず、具体的には、前工程で例示された溶媒と同様のものを例示することができるが、特にジメチルホルムアミドが好ましい。
反応時間は、反応させる基質、反応試剤、反応温度によって異なるが、5分〜60分程度が好ましい。
(1)ホスフィン−dmf−ルテニウム錯体と窒素原子含有配位子(5)とを有機溶媒中に混合して加熱する方法、
(2)ホスフィン−dmf−ルテニウム錯体の有機溶媒溶液を加熱し、窒素原子含有配位子(5)又はその有機溶媒溶液を添加する方法、
(3)窒素原子含有配位子(5)の有機溶媒溶液を加熱し、ホスフィン−dmf−ルテニウム錯体又はその有機溶媒溶液を添加する方法、
等、いずれの方法でも行うことができる。
(1)反応液の容器に貧溶媒を加える方法
(2)貧溶媒の入った容器に反応液を加える方法
(3)反応液と貧溶媒を別容器に同時に連続的に加える方法
等いずれの方法でも行うことができる。
以上のような方法により、目的とするルテニウム錯体(1)を得ることができるが、窒素原子含有配位子(5)中に不純物が含まれていた場合にルテニウム錯体中に例えば、下記式に示すような不純物が含まれていたとしても、そのまま混合物として使用することができるし、下記不純物を分離精製して使用することもできる。
cis―RuCl2(dppb)(ammp)の合成
[2塩化ルテニウム(COD)]多核体([RuCl2(COD)]n)3.05g(純度92%、10ミリモル)、1,4−ビス(ジフェニルホスフィノ)ブタン(dppb)4.26g(10ミリモル)をジメチルホルムアミド15mlに混合し、115−120℃で60分間反応させた。
31P−NMR(161MHz,CDCl3),δ39.0(d,J=37.6Hz),53.4(d,J=37.6Hz)
cis―RuCl2(dppb)(ammp)の合成
[2塩化ルテニウム(COD)]多核体([RuCl2(COD)]n)6.09g(純度92%、20ミリモル)、1,4−ビス(ジフェニルホスフィノ)ブタン(dppb)8.53g(20ミリモル)をジメチルホルムアミド30ml中120−125℃にて60分反応させた。続いて、2−アミノメチル−5−メチルピラジン(AMMP)2.64g(純度98%、21ミリモル)をジメチルホルムアミド5.6mlに溶解し同温にて10分かけて滴下後、さらに60分反応させた。30℃まで冷却した後、酢酸エチル60mlを加え10分攪拌し、生じた沈殿をろ取した。得られた結晶を減圧下乾燥し、cis―RuCl2(dppb)(ammp)の赤橙色結晶(融点290℃ 分解)13.34gを収率92%で得た。
31P−NMR(161MHz,CDCl3),δ39.0(d,J=37.6Hz),53.4(d,J=37.6Hz)
[実施例3]
cis−RuCl2(dppb)(ammp)の合成
[2塩化ルテニウム(COD)]多核体([RuCl2(COD)]n)5.78g(純度97%、20ミリモル)、1,4−ビス(ジフェニルホスフィノ)ブタン(dppb)8.64g(純度99%、20ミリモル)をジメチルホルムアミド30mlに混合し、120−125℃で60分間反応させた。続いて2−アミノメチル−5−メチルピラジン(AMMP)2.64g(純度98%、21ミリモル)をジメチルホルムアミド5.6mlに溶解した溶液を同温にて11分かけて滴下後、さらに60分反応させた。30℃まで冷却した後、生じた沈殿をろ取した。得られた結晶を減圧下乾燥し、cis−RuCl2(dppb)(ammp)の赤橙色結晶12.68gを収率87%で得た。
cis―RuCl2(dppb)(ampz)の合成
[2塩化ルテニウム(COD)]多核体([RuCl2(COD)]n)1.52g(純度92%、5ミリモル)、1,4−ビス(ジフェニルホスフィノ)ブタン(dppb)2.13g(5ミリモル)をジメチルホルムアミド7.5ml中で反応させ、ここへ2−アミノメチルピラジン(AMPZ)0.585(純度98%、5.25ミリモル)をジメチルホルムアミド1.2mlに溶解したものを加えさらに反応させ、酢酸エチル60mlを用いて晶析操作を行った以外は実施例1と同様な方法で、cis―RuCl2(dppb)(ampz)(2.91g)の薄茶色結晶(融点265−266℃分解)を収率91%で得た。
31P−NMR(161MHz,CDCl3),δ34.3(d,J=37.8Hz),53.0(d,J=37.8Hz)
cis―RuCl2(dppb)(Me−bima)の合成
[2塩化ルテニウム(COD)]多核体([RuCl2(COD)]n)0.305g(純度92%、1.0ミリモル)、1,4−ビス(ジフェニルホスフィノ)ブタン(dppb)0.4265g(1.0ミリモル)をジメチルホルムアミド1.5ml中で反応させ、1−メチル−2―ベンズイミダゾールメタンアミン(BIMA)0.193g(純度100%、1.2ミリモル)をジメチルホルムアミド 0.41mlに溶解し加えさらに反応させ、酢酸エチル8.0mlを用いて晶析操作を行った以外は実施例1と同様な方法で、cis―RuCl2(dppb)(Me−bima)の薄茶色結晶(融点236−237℃分解)を収率93%で得た。
31P−NMR(161MHz,CDCl3),δ39.4(d,J=36.8Hz),55.4(d,J=36.8Hz)
cis―RuCl2(dppb)(pica)の合成
[2塩化ルテニウム(COD)]多核体([RuCl2(COD)]n)6.09(純度92%、20ミリモル)、1,4−ビス(ジフェニルホスフィノ)ブタン(dppb)8.53g(20ミリモル)をジメチルホルムアミド30ml中で反応させ、2−ピコリルアミン(PICA)2.32g(純度98%、21ミリモル)をジメチルホルムアミド 4.8mlに溶解し加えさらに反応させ、酢酸エチル60mlを用いて晶析操作を行った以外は実施例1と同様な方法で、cis―RuCl2(dppb)(pica)の薄黄色結晶を収率81%で得た。
31P−NMR(161MHz,CDCl3),δ40.1(d,J=36.9Hz),55.0(d,J=36.9Hz)
Claims (2)
- 下記式(1)
A環は、下記式(2)
又は下記式(3)
下記式(4)
で表されるルテニウム錯体とR1R2R3P及びR4R5R6P(この式中、R1〜R6は、前記式(1)中のR1〜R6と同じ意味を表す。)をジメチルホルムアミド(dmf)中で反応させて、
下記式(5)
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001522846A (ja) * | 1997-11-05 | 2001-11-20 | ニューロサーチ、アクティーゼルスカブ | アザ環−エーテル誘導体及びこれをニコチン性achレセプターモジュレーターとして使用する方法 |
JP2007536338A (ja) * | 2004-05-04 | 2007-12-13 | ユニヴァーシタ’デグリ ステュディ ディ ウーディネ | 2−(アミノメチル)ピリジン及びフォスフィンを有するルテニウムの複合体、その調製方法、並びに触媒としての使用 |
WO2012041215A1 (zh) * | 2010-09-27 | 2012-04-05 | 中山奕安泰医药科技有限公司 | 一种新型含氮杂环配体过渡金属络合物及其制备、催化应用 |
WO2014036702A1 (zh) * | 2012-09-06 | 2014-03-13 | 中山奕安泰医药科技有限公司 | 一类新型含氮配体金属钌络合物及其制备方法和用途 |
JP2015024976A (ja) * | 2013-07-26 | 2015-02-05 | 関東化学株式会社 | 光学活性2級アルコールの製造方法 |
JP2015024975A (ja) * | 2013-07-26 | 2015-02-05 | 関東化学株式会社 | 光学活性2級アルコールの製造方法 |
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Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001522846A (ja) * | 1997-11-05 | 2001-11-20 | ニューロサーチ、アクティーゼルスカブ | アザ環−エーテル誘導体及びこれをニコチン性achレセプターモジュレーターとして使用する方法 |
JP2007536338A (ja) * | 2004-05-04 | 2007-12-13 | ユニヴァーシタ’デグリ ステュディ ディ ウーディネ | 2−(アミノメチル)ピリジン及びフォスフィンを有するルテニウムの複合体、その調製方法、並びに触媒としての使用 |
WO2012041215A1 (zh) * | 2010-09-27 | 2012-04-05 | 中山奕安泰医药科技有限公司 | 一种新型含氮杂环配体过渡金属络合物及其制备、催化应用 |
WO2014036702A1 (zh) * | 2012-09-06 | 2014-03-13 | 中山奕安泰医药科技有限公司 | 一类新型含氮配体金属钌络合物及其制备方法和用途 |
JP2015024976A (ja) * | 2013-07-26 | 2015-02-05 | 関東化学株式会社 | 光学活性2級アルコールの製造方法 |
JP2015024975A (ja) * | 2013-07-26 | 2015-02-05 | 関東化学株式会社 | 光学活性2級アルコールの製造方法 |
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