JP6173702B2 - 光学活性アミン化合物の製造方法 - Google Patents
光学活性アミン化合物の製造方法 Download PDFInfo
- Publication number
- JP6173702B2 JP6173702B2 JP2013017845A JP2013017845A JP6173702B2 JP 6173702 B2 JP6173702 B2 JP 6173702B2 JP 2013017845 A JP2013017845 A JP 2013017845A JP 2013017845 A JP2013017845 A JP 2013017845A JP 6173702 B2 JP6173702 B2 JP 6173702B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- bis
- methoxyphenyl
- hydrogen
- substituent
- 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
- -1 amine compound Chemical class 0.000 title claims description 170
- 238000004519 manufacturing process Methods 0.000 title claims description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims description 121
- 239000001257 hydrogen Substances 0.000 claims description 112
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 96
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 77
- 125000003118 aryl group Chemical group 0.000 claims description 72
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 59
- 125000001424 substituent group Chemical group 0.000 claims description 46
- 150000002430 hydrocarbons Chemical group 0.000 claims description 38
- 125000000217 alkyl group Chemical group 0.000 claims description 32
- 125000003342 alkenyl group Chemical group 0.000 claims description 29
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 27
- 150000002466 imines Chemical class 0.000 claims description 27
- 125000001072 heteroaryl group Chemical group 0.000 claims description 25
- 150000002431 hydrogen Chemical class 0.000 claims description 24
- 125000000304 alkynyl group Chemical group 0.000 claims description 23
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 23
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 21
- 239000012327 Ruthenium complex Substances 0.000 claims description 21
- 125000004432 carbon atom Chemical group C* 0.000 claims description 19
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 18
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 14
- VURFVHCLMJOLKN-UHFFFAOYSA-N Diphosphine Natural products PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 claims description 13
- 239000000010 aprotic solvent Substances 0.000 claims description 13
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 10
- 239000002585 base Substances 0.000 claims description 8
- 239000003446 ligand Substances 0.000 claims description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 7
- 125000004475 heteroaralkyl group Chemical group 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 5
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 4
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 4
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims description 4
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 4
- 150000003512 tertiary amines Chemical class 0.000 claims description 4
- ZHIOKCFUZLQANC-UHFFFAOYSA-N 4-bis(4-methylphenyl)phosphanylpentan-2-yl-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)CC(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 ZHIOKCFUZLQANC-UHFFFAOYSA-N 0.000 claims description 3
- CTYPJIUQROQJBG-UHFFFAOYSA-N 4-diphenylphosphanylpentan-2-yl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)CC(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 CTYPJIUQROQJBG-UHFFFAOYSA-N 0.000 claims description 3
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- OYJAVBPFYHEXDV-UHFFFAOYSA-N 4-bis(4-methoxy-3,5-dimethylphenyl)phosphanylpentan-2-yl-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C1=C(C)C(OC)=C(C)C=C1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)CC(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 OYJAVBPFYHEXDV-UHFFFAOYSA-N 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 description 133
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 73
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 69
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 64
- 238000006243 chemical reaction Methods 0.000 description 58
- 238000004128 high performance liquid chromatography Methods 0.000 description 51
- 239000002904 solvent Substances 0.000 description 40
- 238000009876 asymmetric hydrogenation reaction Methods 0.000 description 37
- 230000015572 biosynthetic process Effects 0.000 description 34
- 238000003786 synthesis reaction Methods 0.000 description 34
- 229910052786 argon Inorganic materials 0.000 description 32
- 239000011521 glass Substances 0.000 description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 29
- 239000000047 product Substances 0.000 description 28
- 229960004592 isopropanol Drugs 0.000 description 24
- 230000003197 catalytic effect Effects 0.000 description 23
- 238000001228 spectrum Methods 0.000 description 23
- FVZVCSNXTFCBQU-UHFFFAOYSA-N phosphanyl Chemical group [PH2] FVZVCSNXTFCBQU-UHFFFAOYSA-N 0.000 description 17
- 239000003054 catalyst Substances 0.000 description 15
- 238000000034 method Methods 0.000 description 13
- QUSNBJAOOMFDIB-UHFFFAOYSA-N monoethyl amine Natural products CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 13
- 125000003545 alkoxy group Chemical group 0.000 description 12
- 238000005984 hydrogenation reaction Methods 0.000 description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 11
- 125000001309 chloro group Chemical group Cl* 0.000 description 10
- 125000005843 halogen group Chemical group 0.000 description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 10
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 9
- BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical compound NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 description 9
- 125000004423 acyloxy group Chemical group 0.000 description 9
- 239000012298 atmosphere Substances 0.000 description 9
- 229910052801 chlorine Inorganic materials 0.000 description 9
- 125000004185 ester group Chemical group 0.000 description 9
- 229910052740 iodine Inorganic materials 0.000 description 9
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 9
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- MSRXKOAPHWUNNM-GFCCVEGCSA-N 2-methoxy-n-[(1r)-1-phenylethyl]aniline Chemical compound COC1=CC=CC=C1N[C@H](C)C1=CC=CC=C1 MSRXKOAPHWUNNM-GFCCVEGCSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- YXIIXSXZNDIDFR-UHFFFAOYSA-N n-(2-methoxyphenyl)-1-phenylethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=CC=C1 YXIIXSXZNDIDFR-UHFFFAOYSA-N 0.000 description 7
- 230000003287 optical effect Effects 0.000 description 7
- VEAFKIYNHVBNIP-UHFFFAOYSA-N 1,3-Diphenylpropane Chemical class C=1C=CC=CC=1CCCC1=CC=CC=C1 VEAFKIYNHVBNIP-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 229910052731 fluorine Inorganic materials 0.000 description 6
- 125000001153 fluoro group Chemical group F* 0.000 description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- OXJQWGDQVWODER-UHFFFAOYSA-N n-[1-(3-chlorophenyl)ethyl]-2-methoxyaniline Chemical compound COC1=CC=CC=C1NC(C)C1=CC=CC(Cl)=C1 OXJQWGDQVWODER-UHFFFAOYSA-N 0.000 description 6
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 5
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 5
- 125000004093 cyano group Chemical group *C#N 0.000 description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 5
- WATIYJMFKFSKGZ-UHFFFAOYSA-N n-(4-methoxyphenyl)-1-phenylethanimine Chemical compound C1=CC(OC)=CC=C1N=C(C)C1=CC=CC=C1 WATIYJMFKFSKGZ-UHFFFAOYSA-N 0.000 description 5
- 125000001624 naphthyl group Chemical group 0.000 description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
- 125000003226 pyrazolyl group Chemical group 0.000 description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 5
- 125000003944 tolyl group Chemical group 0.000 description 5
- YQBXNQKZNIAORQ-UHFFFAOYSA-N 1-(3-chlorophenyl)-n-(2-methoxyphenyl)ethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=CC(Cl)=C1 YQBXNQKZNIAORQ-UHFFFAOYSA-N 0.000 description 4
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 4
- 125000004972 1-butynyl group Chemical group [H]C([H])([H])C([H])([H])C#C* 0.000 description 4
- 125000006017 1-propenyl group Chemical group 0.000 description 4
- 125000000530 1-propynyl group Chemical group [H]C([H])([H])C#C* 0.000 description 4
- 125000000069 2-butynyl group Chemical group [H]C([H])([H])C#CC([H])([H])* 0.000 description 4
- LGAPIWTYEQMRIY-UHFFFAOYSA-N 2-methoxy-n-(1-pyridin-3-ylethyl)aniline Chemical compound COC1=CC=CC=C1NC(C)C1=CC=CN=C1 LGAPIWTYEQMRIY-UHFFFAOYSA-N 0.000 description 4
- XWMYRPGIGSPRSO-UHFFFAOYSA-N 2-methoxy-n-(4-methylpent-3-en-2-yl)aniline Chemical compound COC1=CC=CC=C1NC(C)C=C(C)C XWMYRPGIGSPRSO-UHFFFAOYSA-N 0.000 description 4
- RYZCVDMPQQMIJZ-UHFFFAOYSA-N 2-methoxy-n-[1-(4-methylphenyl)ethyl]aniline Chemical compound COC1=CC=CC=C1NC(C)C1=CC=C(C)C=C1 RYZCVDMPQQMIJZ-UHFFFAOYSA-N 0.000 description 4
- XGBBUPXTIWRTNH-UHFFFAOYSA-N 2-methoxy-n-[1-[4-(trifluoromethyl)phenyl]ethyl]aniline Chemical compound COC1=CC=CC=C1NC(C)C1=CC=C(C(F)(F)F)C=C1 XGBBUPXTIWRTNH-UHFFFAOYSA-N 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 4
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 4
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 4
- 125000000474 3-butynyl group Chemical group [H]C#CC([H])([H])C([H])([H])* 0.000 description 4
- QKBUMGWVDNFABU-GFCCVEGCSA-N 4-methoxy-n-[(1r)-1-phenylethyl]aniline Chemical compound C1=CC(OC)=CC=C1N[C@H](C)C1=CC=CC=C1 QKBUMGWVDNFABU-GFCCVEGCSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 125000002723 alicyclic group Chemical group 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 4
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 4
- 125000004744 butyloxycarbonyl group Chemical group 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 125000001047 cyclobutenyl group Chemical group C1(=CCC1)* 0.000 description 4
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 4
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 4
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 4
- 125000000298 cyclopropenyl group Chemical group [H]C1=C([H])C1([H])* 0.000 description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 4
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 4
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 4
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 4
- 125000002541 furyl group Chemical group 0.000 description 4
- 125000002883 imidazolyl group Chemical group 0.000 description 4
- 125000001041 indolyl group Chemical group 0.000 description 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 4
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 4
- 125000005956 isoquinolyl group Chemical group 0.000 description 4
- 125000005394 methallyl group Chemical group 0.000 description 4
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 4
- 125000002950 monocyclic group Chemical group 0.000 description 4
- SILYBRNOADLIFL-UHFFFAOYSA-N n-[1-(2-fluorophenyl)ethyl]-2-methoxyaniline Chemical compound COC1=CC=CC=C1NC(C)C1=CC=CC=C1F SILYBRNOADLIFL-UHFFFAOYSA-N 0.000 description 4
- YEGXFHGGKURLED-UHFFFAOYSA-N n-[1-(4-chlorophenyl)ethyl]-2-methoxyaniline Chemical compound COC1=CC=CC=C1NC(C)C1=CC=C(Cl)C=C1 YEGXFHGGKURLED-UHFFFAOYSA-N 0.000 description 4
- LVSHCBJXSMBUIN-UHFFFAOYSA-N n-[1-(4-fluorophenyl)ethyl]-2-methoxyaniline Chemical compound COC1=CC=CC=C1NC(C)C1=CC=C(F)C=C1 LVSHCBJXSMBUIN-UHFFFAOYSA-N 0.000 description 4
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 4
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 4
- 125000005412 pyrazyl group Chemical group 0.000 description 4
- 125000004076 pyridyl group Chemical group 0.000 description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 description 4
- 125000000168 pyrrolyl group Chemical group 0.000 description 4
- 125000005493 quinolyl group Chemical group 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 229930195734 saturated hydrocarbon Natural products 0.000 description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 125000000335 thiazolyl group Chemical group 0.000 description 4
- 125000001544 thienyl group Chemical group 0.000 description 4
- 125000001425 triazolyl group Chemical group 0.000 description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 4
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 125000005023 xylyl group Chemical group 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- ACQDEVAGSHHSBG-UHFFFAOYSA-N 2-methoxy-n-(1-pyridin-4-ylethyl)aniline Chemical compound COC1=CC=CC=C1NC(C)C1=CC=NC=C1 ACQDEVAGSHHSBG-UHFFFAOYSA-N 0.000 description 3
- YEBULWSLPRHPRO-CQSZACIVSA-N 2-methoxy-n-[(1r)-1-naphthalen-2-ylethyl]aniline Chemical compound COC1=CC=CC=C1N[C@H](C)C1=CC=C(C=CC=C2)C2=C1 YEBULWSLPRHPRO-CQSZACIVSA-N 0.000 description 3
- IMHLEKTVGMLGTB-CQSZACIVSA-N 2-methoxy-n-[(1r)-1-phenylpropyl]aniline Chemical compound N([C@H](CC)C=1C=CC=CC=1)C1=CC=CC=C1OC IMHLEKTVGMLGTB-CQSZACIVSA-N 0.000 description 3
- NSIRHPLTJMPITQ-UHFFFAOYSA-N 2-methoxy-n-[1-(4-methoxyphenyl)ethyl]aniline Chemical compound C1=CC(OC)=CC=C1C(C)NC1=CC=CC=C1OC NSIRHPLTJMPITQ-UHFFFAOYSA-N 0.000 description 3
- FJFGVASTROGZKI-UHFFFAOYSA-N 3-methyl-n-(1-phenylethyl)aniline Chemical compound C=1C=CC=CC=1C(C)NC1=CC=CC(C)=C1 FJFGVASTROGZKI-UHFFFAOYSA-N 0.000 description 3
- BQUNSIYVDVZZEA-UHFFFAOYSA-N 4-bis(3,5-dimethylphenyl)phosphanylpentan-2-yl-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)CC(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 BQUNSIYVDVZZEA-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- 229940126062 Compound A Drugs 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 238000007872 degassing Methods 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- SHHMVRIBSOJMCK-UHFFFAOYSA-N n-(1-phenylethyl)butan-1-amine Chemical compound CCCCNC(C)C1=CC=CC=C1 SHHMVRIBSOJMCK-UHFFFAOYSA-N 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000003586 protic polar solvent Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- OQAIKCMCNIRGAH-UHFFFAOYSA-N tert-butyl n-[4-[1-(4-chlorophenyl)ethylideneamino]phenyl]-n-methylcarbamate Chemical compound C1=CC(N(C(=O)OC(C)(C)C)C)=CC=C1N=C(C)C1=CC=C(Cl)C=C1 OQAIKCMCNIRGAH-UHFFFAOYSA-N 0.000 description 3
- ZYZHMSJNPCYUTB-CYBMUJFWSA-N (1r)-n-benzyl-1-phenylethanamine Chemical compound N([C@H](C)C=1C=CC=CC=1)CC1=CC=CC=C1 ZYZHMSJNPCYUTB-CYBMUJFWSA-N 0.000 description 2
- MNSJLBYJHGTODD-UHFFFAOYSA-N 1-(2-fluorophenyl)-n-(2-methoxyphenyl)ethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=CC=C1F MNSJLBYJHGTODD-UHFFFAOYSA-N 0.000 description 2
- ZDXPYGZIDVSZRG-UHFFFAOYSA-N 1-(4-chlorophenyl)-n-(2-methoxyphenyl)ethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=C(Cl)C=C1 ZDXPYGZIDVSZRG-UHFFFAOYSA-N 0.000 description 2
- LBJPFOHRGLNHDC-UHFFFAOYSA-N 1-(4-fluorophenyl)-n-(2-methoxyphenyl)ethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=C(F)C=C1 LBJPFOHRGLNHDC-UHFFFAOYSA-N 0.000 description 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- RQEUFEKYXDPUSK-UHFFFAOYSA-N 1-phenylethylamine Chemical compound CC(N)C1=CC=CC=C1 RQEUFEKYXDPUSK-UHFFFAOYSA-N 0.000 description 2
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
- WADSJYLPJPTMLN-UHFFFAOYSA-N 3-(cycloundecen-1-yl)-1,2-diazacycloundec-2-ene Chemical compound C1CCCCCCCCC=C1C1=NNCCCCCCCC1 WADSJYLPJPTMLN-UHFFFAOYSA-N 0.000 description 2
- JQCZMVCDTNSDJU-UHFFFAOYSA-N 3-bromo-n-[1-(4-chloro-3-methylphenyl)ethyl]aniline Chemical compound C=1C=C(Cl)C(C)=CC=1C(C)NC1=CC=CC(Br)=C1 JQCZMVCDTNSDJU-UHFFFAOYSA-N 0.000 description 2
- WMMSGYSFSFERDX-LLVKDONJSA-N 4-bromo-n-[(1r)-1-phenylethyl]aniline Chemical compound N([C@H](C)C=1C=CC=CC=1)C1=CC=C(Br)C=C1 WMMSGYSFSFERDX-LLVKDONJSA-N 0.000 description 2
- QKBUMGWVDNFABU-LBPRGKRZSA-N 4-methoxy-n-[(1s)-1-phenylethyl]aniline Chemical compound C1=CC(OC)=CC=C1N[C@@H](C)C1=CC=CC=C1 QKBUMGWVDNFABU-LBPRGKRZSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 239000003905 agrochemical Chemical class 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 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
- 239000003759 ester based solvent Substances 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- CBXWICRJSHEQJT-UHFFFAOYSA-N n,1-diphenylethanimine Chemical compound C=1C=CC=CC=1C(C)=NC1=CC=CC=C1 CBXWICRJSHEQJT-UHFFFAOYSA-N 0.000 description 2
- VPXUTEFJZOHQCU-UHFFFAOYSA-N n-(2-methoxyphenyl)-1-(4-methoxyphenyl)ethanimine Chemical compound C1=CC(OC)=CC=C1C(C)=NC1=CC=CC=C1OC VPXUTEFJZOHQCU-UHFFFAOYSA-N 0.000 description 2
- VPOVUBNVERAUJB-UHFFFAOYSA-N n-(2-methoxyphenyl)-1-(4-methylphenyl)ethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=C(C)C=C1 VPOVUBNVERAUJB-UHFFFAOYSA-N 0.000 description 2
- LUGHADJJARIZAA-UHFFFAOYSA-N n-(2-methoxyphenyl)-1-[4-(trifluoromethyl)phenyl]ethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=C(C(F)(F)F)C=C1 LUGHADJJARIZAA-UHFFFAOYSA-N 0.000 description 2
- VBOQUYIJVROIQD-UHFFFAOYSA-N n-(2-methoxyphenyl)-1-naphthalen-2-ylethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=C(C=CC=C2)C2=C1 VBOQUYIJVROIQD-UHFFFAOYSA-N 0.000 description 2
- HEKCIMCPWYCHOX-UHFFFAOYSA-N n-(2-methoxyphenyl)-1-phenylpropan-1-imine Chemical compound C=1C=CC=CC=1C(CC)=NC1=CC=CC=C1OC HEKCIMCPWYCHOX-UHFFFAOYSA-N 0.000 description 2
- PQUAKNUXTNIERW-UHFFFAOYSA-N n-(2-methoxyphenyl)-1-pyridin-3-ylethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=CN=C1 PQUAKNUXTNIERW-UHFFFAOYSA-N 0.000 description 2
- SJVOATFHRLZSHL-UHFFFAOYSA-N n-(2-methoxyphenyl)-1-pyridin-4-ylethanimine Chemical compound COC1=CC=CC=C1N=C(C)C1=CC=NC=C1 SJVOATFHRLZSHL-UHFFFAOYSA-N 0.000 description 2
- HKBHKFMEEPSIOZ-UHFFFAOYSA-N n-(2-methoxyphenyl)-4-methylpent-3-en-2-imine Chemical compound COC1=CC=CC=C1N=C(C)C=C(C)C HKBHKFMEEPSIOZ-UHFFFAOYSA-N 0.000 description 2
- LYNHYJGMECTOCZ-UHFFFAOYSA-N n-(3-bromophenyl)-1-(4-chloro-3-methylphenyl)ethanimine Chemical compound C=1C=C(Cl)C(C)=CC=1C(C)=NC1=CC=CC(Br)=C1 LYNHYJGMECTOCZ-UHFFFAOYSA-N 0.000 description 2
- YYSXZCAHUANNEB-UHFFFAOYSA-N n-(3-methylphenyl)-1-phenylethanimine Chemical compound C=1C=CC=CC=1C(C)=NC1=CC=CC(C)=C1 YYSXZCAHUANNEB-UHFFFAOYSA-N 0.000 description 2
- NVGPJBDDPVXJDJ-UHFFFAOYSA-N n-(4-bromophenyl)-1-phenylethanimine Chemical compound C=1C=CC=CC=1C(C)=NC1=CC=C(Br)C=C1 NVGPJBDDPVXJDJ-UHFFFAOYSA-N 0.000 description 2
- IUERBKSXAYWVGE-GFCCVEGCSA-N n-[(1r)-1-phenylethyl]aniline Chemical compound N([C@H](C)C=1C=CC=CC=1)C1=CC=CC=C1 IUERBKSXAYWVGE-GFCCVEGCSA-N 0.000 description 2
- JATCPLSBWDXCNE-UHFFFAOYSA-N n-benzyl-1-phenylethanimine Chemical compound C=1C=CC=CC=1C(C)=NCC1=CC=CC=C1 JATCPLSBWDXCNE-UHFFFAOYSA-N 0.000 description 2
- IBZXCHMWVMJGLP-UHFFFAOYSA-N n-butyl-1-phenylethanimine Chemical compound CCCCN=C(C)C1=CC=CC=C1 IBZXCHMWVMJGLP-UHFFFAOYSA-N 0.000 description 2
- JFDMUIIZYZDKQW-UHFFFAOYSA-N n-butyl-n-(1-phenylethyl)acetamide Chemical compound CCCCN(C(C)=O)C(C)C1=CC=CC=C1 JFDMUIIZYZDKQW-UHFFFAOYSA-N 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 239000013110 organic ligand Substances 0.000 description 2
- 125000003884 phenylalkyl group Chemical group 0.000 description 2
- 125000004344 phenylpropyl group Chemical group 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- MAZOHJVAXBNBPX-UHFFFAOYSA-N ruthenium hydrochloride Chemical compound Cl.[Ru] MAZOHJVAXBNBPX-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- WPEXKMAYUSUXIF-UHFFFAOYSA-N (3-diphenylphosphanyl-1,3-diphenylpropyl)-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)CC(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 WPEXKMAYUSUXIF-UHFFFAOYSA-N 0.000 description 1
- NXKMRSSEICPSAD-UHFFFAOYSA-N (3-diphenylphosphanyl-2,2-dimethyl-1,3-diphenylpropyl)-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(C)(C)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 NXKMRSSEICPSAD-UHFFFAOYSA-N 0.000 description 1
- AUBNYIIOYJCWHG-UHFFFAOYSA-N (4-diphenylphosphanyl-3,3-diethylpentan-2-yl)-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(CC)(CC)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 AUBNYIIOYJCWHG-UHFFFAOYSA-N 0.000 description 1
- CQBYZZOJPDVOOR-UHFFFAOYSA-N (4-diphenylphosphanyl-3,3-dimethylpentan-2-yl)-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(C)(C)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 CQBYZZOJPDVOOR-UHFFFAOYSA-N 0.000 description 1
- BYBKWMOWKHHENJ-UHFFFAOYSA-N (4-diphenylphosphanyl-3-ethylpentan-2-yl)-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(CC)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 BYBKWMOWKHHENJ-UHFFFAOYSA-N 0.000 description 1
- WREFXNGPCLHVSW-UHFFFAOYSA-N (4-diphenylphosphanyl-3-methylpentan-2-yl)-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(C)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 WREFXNGPCLHVSW-UHFFFAOYSA-N 0.000 description 1
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
- 125000006649 (C2-C20) alkynyl group Chemical group 0.000 description 1
- WDYGPMAMBXJESZ-UHFFFAOYSA-N 1,1-bis(4-methoxyphenyl)-3-methylbutane-1,2-diamine Chemical compound C1=CC(OC)=CC=C1C(N)(C(N)C(C)C)C1=CC=C(OC)C=C1 WDYGPMAMBXJESZ-UHFFFAOYSA-N 0.000 description 1
- HBSXDFSJTIINEG-UHFFFAOYSA-N 1,2-bis(2-fluorophenyl)ethane-1,2-diamine Chemical compound C=1C=CC=C(F)C=1C(N)C(N)C1=CC=CC=C1F HBSXDFSJTIINEG-UHFFFAOYSA-N 0.000 description 1
- CTMKVJFFLNHDQE-UHFFFAOYSA-N 1,2-bis(2-methoxyphenyl)ethane-1,2-diamine Chemical compound COC1=CC=CC=C1C(N)C(N)C1=CC=CC=C1OC CTMKVJFFLNHDQE-UHFFFAOYSA-N 0.000 description 1
- HKBNVGISGVWESI-UHFFFAOYSA-N 1,2-bis(2-methylphenyl)ethane-1,2-diamine Chemical compound CC1=CC=CC=C1C(N)C(N)C1=CC=CC=C1C HKBNVGISGVWESI-UHFFFAOYSA-N 0.000 description 1
- POWCVEXEFGJWNW-UHFFFAOYSA-N 1,2-bis(3,5-dimethylphenyl)ethane-1,2-diamine Chemical compound CC1=CC(C)=CC(C(N)C(N)C=2C=C(C)C=C(C)C=2)=C1 POWCVEXEFGJWNW-UHFFFAOYSA-N 0.000 description 1
- QMIJYVGZCWHVSW-UHFFFAOYSA-N 1,2-bis(3-fluorophenyl)ethane-1,2-diamine Chemical compound C=1C=CC(F)=CC=1C(N)C(N)C1=CC=CC(F)=C1 QMIJYVGZCWHVSW-UHFFFAOYSA-N 0.000 description 1
- VLIGRZTVNRBXFH-UHFFFAOYSA-N 1,2-bis(3-methoxyphenyl)ethane-1,2-diamine Chemical compound COC1=CC=CC(C(N)C(N)C=2C=C(OC)C=CC=2)=C1 VLIGRZTVNRBXFH-UHFFFAOYSA-N 0.000 description 1
- DWKHQEHNAPMAGG-UHFFFAOYSA-N 1,2-bis(4-fluorophenyl)ethane-1,2-diamine Chemical compound C=1C=C(F)C=CC=1C(N)C(N)C1=CC=C(F)C=C1 DWKHQEHNAPMAGG-UHFFFAOYSA-N 0.000 description 1
- ZWMPRHYHRAUVGY-UHFFFAOYSA-N 1,2-bis(4-methoxyphenyl)ethane-1,2-diamine Chemical compound C1=CC(OC)=CC=C1C(N)C(N)C1=CC=C(OC)C=C1 ZWMPRHYHRAUVGY-UHFFFAOYSA-N 0.000 description 1
- UQUZLWQGLCLOBD-UHFFFAOYSA-N 1,2-bis(4-methylphenyl)ethane-1,2-diamine Chemical compound C1=CC(C)=CC=C1C(N)C(N)C1=CC=C(C)C=C1 UQUZLWQGLCLOBD-UHFFFAOYSA-N 0.000 description 1
- POCXSZQENPZZJP-UHFFFAOYSA-N 1,2-bis[3-(trifluoromethyl)phenyl]ethane-1,2-diamine Chemical compound C=1C=CC(C(F)(F)F)=CC=1C(N)C(N)C1=CC=CC(C(F)(F)F)=C1 POCXSZQENPZZJP-UHFFFAOYSA-N 0.000 description 1
- MLOYHHKFBCFAAD-UHFFFAOYSA-N 1,2-bis[4-(trifluoromethyl)phenyl]ethane-1,2-diamine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(N)C(N)C1=CC=C(C(F)(F)F)C=C1 MLOYHHKFBCFAAD-UHFFFAOYSA-N 0.000 description 1
- PONXTPCRRASWKW-UHFFFAOYSA-N 1,2-diphenylethane-1,2-diamine Chemical compound C=1C=CC=CC=1C(N)C(N)C1=CC=CC=C1 PONXTPCRRASWKW-UHFFFAOYSA-N 0.000 description 1
- JTDGKQNNPKXKII-UHFFFAOYSA-N 1-(4-methoxyphenyl)ethanamine Chemical compound COC1=CC=C(C(C)N)C=C1 JTDGKQNNPKXKII-UHFFFAOYSA-N 0.000 description 1
- UHDGCWIWMRVCDJ-UHFFFAOYSA-N 1-beta-D-Xylofuranosyl-NH-Cytosine Natural products O=C1N=C(N)C=CN1C1C(O)C(O)C(CO)O1 UHDGCWIWMRVCDJ-UHFFFAOYSA-N 0.000 description 1
- CRVBQABBEKLFIN-UHFFFAOYSA-N 1-phenylethane-1,2-diamine Chemical compound NCC(N)C1=CC=CC=C1 CRVBQABBEKLFIN-UHFFFAOYSA-N 0.000 description 1
- DJYSEQMMCZAKGT-UHFFFAOYSA-N 2,3,3-trimethylhexane Chemical compound CCCC(C)(C)C(C)C DJYSEQMMCZAKGT-UHFFFAOYSA-N 0.000 description 1
- SKIIKRJAQOSWFT-UHFFFAOYSA-N 2-[3-[1-(2,2-difluoroethyl)piperidin-4-yl]oxy-4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound FC(CN1CCC(CC1)OC1=NN(C=C1C=1C=NC(=NC=1)NC1CC2=CC=CC=C2C1)CC(=O)N1CC2=C(CC1)NN=N2)F SKIIKRJAQOSWFT-UHFFFAOYSA-N 0.000 description 1
- YEBULWSLPRHPRO-AWEZNQCLSA-N 2-methoxy-n-[(1s)-1-naphthalen-2-ylethyl]aniline Chemical compound COC1=CC=CC=C1N[C@@H](C)C1=CC=C(C=CC=C2)C2=C1 YEBULWSLPRHPRO-AWEZNQCLSA-N 0.000 description 1
- IMHLEKTVGMLGTB-AWEZNQCLSA-N 2-methoxy-n-[(1s)-1-phenylpropyl]aniline Chemical compound N([C@@H](CC)C=1C=CC=CC=1)C1=CC=CC=C1OC IMHLEKTVGMLGTB-AWEZNQCLSA-N 0.000 description 1
- DKASDMAHYNJHHX-UHFFFAOYSA-N 3-(1-diphenylphosphanylethyl)hexan-2-yl-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(CCC)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 DKASDMAHYNJHHX-UHFFFAOYSA-N 0.000 description 1
- LIRMWKKKRKVIPI-UHFFFAOYSA-N 3-[1-bis(3,5-diethylphenyl)phosphanylethyl]hexan-2-yl-bis(3,5-diethylphenyl)phosphane Chemical compound C=1C(CC)=CC(CC)=CC=1P(C=1C=C(CC)C=C(CC)C=1)C(C)C(CCC)C(C)P(C=1C=C(CC)C=C(CC)C=1)C1=CC(CC)=CC(CC)=C1 LIRMWKKKRKVIPI-UHFFFAOYSA-N 0.000 description 1
- GKZZWXWHUFNYRY-UHFFFAOYSA-N 3-[1-bis(4-methylphenyl)phosphanylethyl]hexan-2-yl-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(CCC)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 GKZZWXWHUFNYRY-UHFFFAOYSA-N 0.000 description 1
- BFILOVVITSZEOF-UHFFFAOYSA-N 3-[1-bis(4-tert-butylphenyl)phosphanylethyl]hexan-2-yl-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C)C(CCC)C(C)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 BFILOVVITSZEOF-UHFFFAOYSA-N 0.000 description 1
- 125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 description 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 1
- RIVMBFKOBFMDQT-UHFFFAOYSA-N 4-bis(3,5-diethylphenyl)phosphanylpentan-2-yl-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C)CC(C)P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)=C1 RIVMBFKOBFMDQT-UHFFFAOYSA-N 0.000 description 1
- NOLMSXJJRKOIOF-UHFFFAOYSA-N 4-bis(4-tert-butylphenyl)phosphanylpentan-2-yl-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C)CC(C)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 NOLMSXJJRKOIOF-UHFFFAOYSA-N 0.000 description 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 description 1
- RUKVBHPDMGTGOS-UHFFFAOYSA-N CC(CCCP(C1=CC(C)=CC(C)=C1)C1=CC(C)=CC(C)=C1)P(C1=CC(C)=CC(C)=C1)C1=CC(C)=CC(C)=C1 Chemical compound CC(CCCP(C1=CC(C)=CC(C)=C1)C1=CC(C)=CC(C)=C1)P(C1=CC(C)=CC(C)=C1)C1=CC(C)=CC(C)=C1 RUKVBHPDMGTGOS-UHFFFAOYSA-N 0.000 description 1
- FAOMKERFTFPESP-UHFFFAOYSA-N CCC(C(C)C)(C(C)(CO)P(C1=CC(CC)=CC(CC)=C1)C1=CC(CC)=CC(CC)=C1)C(C)(CO)P(C1=CC(CC)=CC(CC)=C1)C1=CC(CC)=CC(CC)=C1 Chemical compound CCC(C(C)C)(C(C)(CO)P(C1=CC(CC)=CC(CC)=C1)C1=CC(CC)=CC(CC)=C1)C(C)(CO)P(C1=CC(CC)=CC(CC)=C1)C1=CC(CC)=CC(CC)=C1 FAOMKERFTFPESP-UHFFFAOYSA-N 0.000 description 1
- MKSGJVQDYGRDNF-UHFFFAOYSA-N CCC(C)CCP(C1=CC=C(C=C1)C(C)(C)C)C2=CC=C(C=C2)C(C)(C)C Chemical compound CCC(C)CCP(C1=CC=C(C=C1)C(C)(C)C)C2=CC=C(C=C2)C(C)(C)C MKSGJVQDYGRDNF-UHFFFAOYSA-N 0.000 description 1
- NHGGDGOMJJFCFC-UHFFFAOYSA-N CCC(CC1=CC=CC=C1)(C(C)C)C(C2=CC=CC=C2)P(C3=CC(=C(C(=C3)C)OC)C)C4=CC(=C(C(=C4)C)OC)C Chemical compound CCC(CC1=CC=CC=C1)(C(C)C)C(C2=CC=CC=C2)P(C3=CC(=C(C(=C3)C)OC)C)C4=CC(=C(C(=C4)C)OC)C NHGGDGOMJJFCFC-UHFFFAOYSA-N 0.000 description 1
- NRXKHOWGKXQXFS-UHFFFAOYSA-N CCCC(CC)CC(C1=CC(=C(C(=C1)C)OC)C)P Chemical compound CCCC(CC)CC(C1=CC(=C(C(=C1)C)OC)C)P NRXKHOWGKXQXFS-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N DMBan Natural products CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 1
- NEAPKZHDYMQZCB-UHFFFAOYSA-N N-[2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]ethyl]-2-oxo-3H-1,3-benzoxazole-6-carboxamide Chemical compound C1CN(CCN1CCNC(=O)C2=CC3=C(C=C2)NC(=O)O3)C4=CN=C(N=C4)NC5CC6=CC=CC=C6C5 NEAPKZHDYMQZCB-UHFFFAOYSA-N 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- VCZSNVRYEHOLSV-UHFFFAOYSA-N [2-[bis(3,5-diethylphenyl)phosphanyl-phenylmethyl]-1-phenyl-2-propylpentyl]-bis(3,5-diethylphenyl)phosphane Chemical compound C=1C(CC)=CC(CC)=CC=1P(C=1C=C(CC)C=C(CC)C=1)C(C=1C=CC=CC=1)C(CCC)(CCC)C(C=1C=CC=CC=1)P(C=1C=C(CC)C=C(CC)C=1)C1=CC(CC)=CC(CC)=C1 VCZSNVRYEHOLSV-UHFFFAOYSA-N 0.000 description 1
- WFXHYYVJMSYCNE-UHFFFAOYSA-N [2-[bis(3,5-diethylphenyl)phosphanyl-phenylmethyl]-1-phenylbutyl]-bis(3,5-diethylphenyl)phosphane Chemical compound C=1C(CC)=CC(CC)=CC=1P(C=1C=C(CC)C=C(CC)C=1)C(C=1C=CC=CC=1)C(CC)C(C=1C=CC=CC=1)P(C=1C=C(CC)C=C(CC)C=1)C1=CC(CC)=CC(CC)=C1 WFXHYYVJMSYCNE-UHFFFAOYSA-N 0.000 description 1
- ULKPRKBMNQAOLQ-UHFFFAOYSA-N [2-[bis(3,5-diethylphenyl)phosphanyl-phenylmethyl]-2-ethyl-1-phenylbutyl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C=2C=CC=CC=2)C(CC)(CC)C(P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=CC=CC=2)C=2C=C(CC)C=C(CC)C=2)=C1 ULKPRKBMNQAOLQ-UHFFFAOYSA-N 0.000 description 1
- PVOGUASDTLMYCO-UHFFFAOYSA-N [2-[bis(3,5-diethylphenyl)phosphanyl-phenylmethyl]-2-ethyl-1-phenylpentyl]-bis(3,5-diethylphenyl)phosphane Chemical compound C=1C(CC)=CC(CC)=CC=1P(C=1C=C(CC)C=C(CC)C=1)C(C=1C=CC=CC=1)C(CC)(CCC)C(C=1C=CC=CC=1)P(C=1C=C(CC)C=C(CC)C=1)C1=CC(CC)=CC(CC)=C1 PVOGUASDTLMYCO-UHFFFAOYSA-N 0.000 description 1
- JERXVEMMCBPFDP-UHFFFAOYSA-N [2-[bis(3,5-diethylphenyl)phosphanyl-phenylmethyl]-2-ethyl-3-methyl-1-phenylbutyl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C=2C=CC=CC=2)C(CC)(C(C)C)C(P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=CC=CC=2)C=2C=C(CC)C=C(CC)C=2)=C1 JERXVEMMCBPFDP-UHFFFAOYSA-N 0.000 description 1
- YPUSSMAZUOJERM-UHFFFAOYSA-N [2-[bis(3,5-diethylphenyl)phosphanyl-phenylmethyl]-2-methyl-1-phenylbutyl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C=2C=CC=CC=2)C(C)(CC)C(P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=CC=CC=2)C=2C=C(CC)C=C(CC)C=2)=C1 YPUSSMAZUOJERM-UHFFFAOYSA-N 0.000 description 1
- YSZQFEOHRNVEIN-UHFFFAOYSA-N [2-[bis(3,5-diethylphenyl)phosphanyl-phenylmethyl]-2-methyl-1-phenylpentyl]-bis(3,5-diethylphenyl)phosphane Chemical compound C=1C(CC)=CC(CC)=CC=1P(C=1C=C(CC)C=C(CC)C=1)C(C=1C=CC=CC=1)C(C)(CCC)C(C=1C=CC=CC=1)P(C=1C=C(CC)C=C(CC)C=1)C1=CC(CC)=CC(CC)=C1 YSZQFEOHRNVEIN-UHFFFAOYSA-N 0.000 description 1
- HCXXRPHSXMQUGY-UHFFFAOYSA-N [2-[bis(3,5-diethylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenyl-2-propan-2-ylbutyl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C=2C=CC=CC=2)C(C(C)C)(C(C)C)C(P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=CC=CC=2)C=2C=C(CC)C=C(CC)C=2)=C1 HCXXRPHSXMQUGY-UHFFFAOYSA-N 0.000 description 1
- WJOUJJWJRYUMEN-UHFFFAOYSA-N [2-[bis(3,5-diethylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenylbutyl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C(C(C)C)C(P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=CC=CC=2)C=2C=CC=CC=2)C=2C=C(CC)C=C(CC)C=2)=C1 WJOUJJWJRYUMEN-UHFFFAOYSA-N 0.000 description 1
- AAMCOZWAABMDIZ-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-1-phenyl-2-propan-2-ylpentyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(C(C)C)(CCC)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 AAMCOZWAABMDIZ-UHFFFAOYSA-N 0.000 description 1
- RHLYTTHEUBUZPM-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-1-phenylbutyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(CC)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 RHLYTTHEUBUZPM-UHFFFAOYSA-N 0.000 description 1
- WSVLBKCYINLNGL-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-1-phenylpentyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(CCC)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 WSVLBKCYINLNGL-UHFFFAOYSA-N 0.000 description 1
- HIOCAISZRXEMPQ-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-2,3-dimethyl-1-phenylbutyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(C)(C(C)C)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 HIOCAISZRXEMPQ-UHFFFAOYSA-N 0.000 description 1
- ZLTBXQBKKDLUCV-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-2-ethyl-1-phenylbutyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(CC)(CC)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 ZLTBXQBKKDLUCV-UHFFFAOYSA-N 0.000 description 1
- FFMKXWIQWMYSDN-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-2-ethyl-1-phenylpentyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(CC)(CCC)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 FFMKXWIQWMYSDN-UHFFFAOYSA-N 0.000 description 1
- XTIHICRGHPVJMZ-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-2-methyl-1-phenylbutyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(C)(CC)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 XTIHICRGHPVJMZ-UHFFFAOYSA-N 0.000 description 1
- FRAQLEPXOUZWBA-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-2-methyl-1-phenylpentyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(C)(CCC)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 FRAQLEPXOUZWBA-UHFFFAOYSA-N 0.000 description 1
- QWRJMOIPLRUIRB-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenyl-2-propan-2-ylbutyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(C(C)C)(C(C)C)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 QWRJMOIPLRUIRB-UHFFFAOYSA-N 0.000 description 1
- AQEQKEWHSPTUFX-UHFFFAOYSA-N [2-[bis(3,5-dimethylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenylbutyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(C(C)C)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 AQEQKEWHSPTUFX-UHFFFAOYSA-N 0.000 description 1
- ZJAIMVUUERPYFE-UHFFFAOYSA-N [2-[bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-phenylmethyl]-1-phenyl-2-propan-2-ylpentyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C=1C=CC=CC=1)C(C(C)C)(CCC)C(C=1C=CC=CC=1)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 ZJAIMVUUERPYFE-UHFFFAOYSA-N 0.000 description 1
- BEPOMDLSBXSZNP-UHFFFAOYSA-N [2-[bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-phenylmethyl]-1-phenyl-2-propylpentyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C=1C=CC=CC=1)C(CCC)(CCC)C(C=1C=CC=CC=1)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 BEPOMDLSBXSZNP-UHFFFAOYSA-N 0.000 description 1
- PLRVQVARQWSEOB-UHFFFAOYSA-N [2-[bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-phenylmethyl]-1-phenylbutyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C=1C=CC=CC=1)C(CC)C(C=1C=CC=CC=1)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 PLRVQVARQWSEOB-UHFFFAOYSA-N 0.000 description 1
- QFWVVZSLNWMQFX-UHFFFAOYSA-N [2-[bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-phenylmethyl]-1-phenylpentyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C=1C=CC=CC=1)C(CCC)C(C=1C=CC=CC=1)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 QFWVVZSLNWMQFX-UHFFFAOYSA-N 0.000 description 1
- MBUVZCWCTJQSPQ-UHFFFAOYSA-N [2-[bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-phenylmethyl]-2,3-dimethyl-1-phenylbutyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C1=C(C)C(OC)=C(C)C=C1P(C=1C=C(C)C(OC)=C(C)C=1)C(C(C)(C(C)C)C(P(C=1C=C(C)C(OC)=C(C)C=1)C=1C=C(C)C(OC)=C(C)C=1)C=1C=CC=CC=1)C1=CC=CC=C1 MBUVZCWCTJQSPQ-UHFFFAOYSA-N 0.000 description 1
- ZNKYNHAYNGHVCZ-UHFFFAOYSA-N [2-[bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-phenylmethyl]-2-ethyl-1-phenylpentyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C=1C=CC=CC=1)C(CC)(CCC)C(C=1C=CC=CC=1)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 ZNKYNHAYNGHVCZ-UHFFFAOYSA-N 0.000 description 1
- BUHQBXVYFGTVDS-UHFFFAOYSA-N [2-[bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-phenylmethyl]-2-methyl-1-phenylbutyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C=1C=CC=CC=1)C(C)(CC)C(C=1C=CC=CC=1)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 BUHQBXVYFGTVDS-UHFFFAOYSA-N 0.000 description 1
- JQNCJWDFEACZOI-UHFFFAOYSA-N [2-[bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenyl-2-propan-2-ylbutyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C1=C(C)C(OC)=C(C)C=C1P(C=1C=C(C)C(OC)=C(C)C=1)C(C(C(C)C)(C(C)C)C(P(C=1C=C(C)C(OC)=C(C)C=1)C=1C=C(C)C(OC)=C(C)C=1)C=1C=CC=CC=1)C1=CC=CC=C1 JQNCJWDFEACZOI-UHFFFAOYSA-N 0.000 description 1
- QZNFRZHOSXFCLD-UHFFFAOYSA-N [2-[bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenylbutyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C1=C(C)C(OC)=C(C)C=C1P(C=1C=C(C)C(OC)=C(C)C=1)C(C=1C=CC=CC=1)C(C(C)C)C(C=1C=CC=CC=1)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 QZNFRZHOSXFCLD-UHFFFAOYSA-N 0.000 description 1
- IVYGOJOVQHSDFF-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-1-phenyl-2-propan-2-ylpentyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(C(C)C)(CCC)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 IVYGOJOVQHSDFF-UHFFFAOYSA-N 0.000 description 1
- KHTSRJWARDCEEX-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-1-phenylbutyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(CC)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 KHTSRJWARDCEEX-UHFFFAOYSA-N 0.000 description 1
- USLBUBNERCGKFL-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-1-phenylpentyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(CCC)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 USLBUBNERCGKFL-UHFFFAOYSA-N 0.000 description 1
- GKZUGNSPZBOVMI-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-2,3-dimethyl-1-phenylbutyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(C)(C(C)C)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 GKZUGNSPZBOVMI-UHFFFAOYSA-N 0.000 description 1
- KXGRYZVGWIWQOC-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-2-ethyl-1-phenylbutyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(CC)(CC)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 KXGRYZVGWIWQOC-UHFFFAOYSA-N 0.000 description 1
- KGZZWGXDEOFHSI-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-2-ethyl-1-phenylpentyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(CC)(CCC)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 KGZZWGXDEOFHSI-UHFFFAOYSA-N 0.000 description 1
- VXUKVXKDYZWRSS-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-2-methyl-1-phenylbutyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(C)(CC)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 VXUKVXKDYZWRSS-UHFFFAOYSA-N 0.000 description 1
- WBTDKJGJTWJAQP-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-2-methyl-1-phenylpentyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(C)(CCC)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 WBTDKJGJTWJAQP-UHFFFAOYSA-N 0.000 description 1
- NPXANIULGSLJDK-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenyl-2-propan-2-ylbutyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(C(C)C)(C(C)C)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 NPXANIULGSLJDK-UHFFFAOYSA-N 0.000 description 1
- IVOPXXVEFMBQNN-UHFFFAOYSA-N [2-[bis(4-methylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenylbutyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(C(C)C)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 IVOPXXVEFMBQNN-UHFFFAOYSA-N 0.000 description 1
- GJGNOJQVSOKLDC-UHFFFAOYSA-N [2-[bis(4-tert-butylphenyl)phosphanyl-phenylmethyl]-1-phenyl-2-propan-2-ylpentyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(C(C)C)(CCC)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 GJGNOJQVSOKLDC-UHFFFAOYSA-N 0.000 description 1
- WMHNKLFYDOWLNT-UHFFFAOYSA-N [2-[bis(4-tert-butylphenyl)phosphanyl-phenylmethyl]-1-phenyl-2-propylpentyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(CCC)(CCC)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 WMHNKLFYDOWLNT-UHFFFAOYSA-N 0.000 description 1
- JGSJNTZXJDUUES-UHFFFAOYSA-N [2-[bis(4-tert-butylphenyl)phosphanyl-phenylmethyl]-1-phenylbutyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(CC)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 JGSJNTZXJDUUES-UHFFFAOYSA-N 0.000 description 1
- NBFPCSACNOWKOX-UHFFFAOYSA-N [2-[bis(4-tert-butylphenyl)phosphanyl-phenylmethyl]-2-ethyl-1-phenylbutyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(CC)(CC)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 NBFPCSACNOWKOX-UHFFFAOYSA-N 0.000 description 1
- PBLDQLKEQLZOOG-UHFFFAOYSA-N [2-[bis(4-tert-butylphenyl)phosphanyl-phenylmethyl]-2-methyl-1-phenylbutyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(C)(CC)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 PBLDQLKEQLZOOG-UHFFFAOYSA-N 0.000 description 1
- HIKPHLNKYPDIJJ-UHFFFAOYSA-N [2-[bis(4-tert-butylphenyl)phosphanyl-phenylmethyl]-2-methyl-1-phenylpentyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(C)(CCC)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 HIKPHLNKYPDIJJ-UHFFFAOYSA-N 0.000 description 1
- WYUDARHKEBMRFE-UHFFFAOYSA-N [2-[bis(4-tert-butylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenyl-2-propan-2-ylbutyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(C(C)C)(C(C)C)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 WYUDARHKEBMRFE-UHFFFAOYSA-N 0.000 description 1
- FYXUMTFLBDMOEA-UHFFFAOYSA-N [2-[bis(4-tert-butylphenyl)phosphanyl-phenylmethyl]-3-methyl-1-phenylbutyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(C(C)C)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 FYXUMTFLBDMOEA-UHFFFAOYSA-N 0.000 description 1
- BXECUPNQMWUCAM-UHFFFAOYSA-N [2-[diphenylphosphanyl(phenyl)methyl]-1-phenyl-2-propylpentyl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(CCC)(CCC)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 BXECUPNQMWUCAM-UHFFFAOYSA-N 0.000 description 1
- VEJAGUNVXLZRPW-UHFFFAOYSA-N [2-[diphenylphosphanyl(phenyl)methyl]-1-phenylbutyl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(CC)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 VEJAGUNVXLZRPW-UHFFFAOYSA-N 0.000 description 1
- RMEHYBRNNNMCFH-UHFFFAOYSA-N [2-[diphenylphosphanyl(phenyl)methyl]-1-phenylpentyl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(CCC)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 RMEHYBRNNNMCFH-UHFFFAOYSA-N 0.000 description 1
- VMNOCTSCGDOMKW-UHFFFAOYSA-N [2-[diphenylphosphanyl(phenyl)methyl]-2,3-dimethyl-1-phenylbutyl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(C)(C(C)C)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 VMNOCTSCGDOMKW-UHFFFAOYSA-N 0.000 description 1
- BWFYFFXWXZBDSI-UHFFFAOYSA-N [2-[diphenylphosphanyl(phenyl)methyl]-2-ethyl-1-phenylbutyl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(CC)(CC)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 BWFYFFXWXZBDSI-UHFFFAOYSA-N 0.000 description 1
- IRVDYQWYUAJQMS-UHFFFAOYSA-N [2-[diphenylphosphanyl(phenyl)methyl]-2-ethyl-1-phenylpentyl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(CC)(CCC)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 IRVDYQWYUAJQMS-UHFFFAOYSA-N 0.000 description 1
- WYUFCGKONVLYMX-UHFFFAOYSA-N [2-[diphenylphosphanyl(phenyl)methyl]-2-methyl-1-phenylbutyl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(C)(CC)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 WYUFCGKONVLYMX-UHFFFAOYSA-N 0.000 description 1
- LNUCRMPMZYHAGO-UHFFFAOYSA-N [2-[diphenylphosphanyl(phenyl)methyl]-2-methyl-1-phenylpentyl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(C)(CCC)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 LNUCRMPMZYHAGO-UHFFFAOYSA-N 0.000 description 1
- ZJOSFSQAMSLVEL-UHFFFAOYSA-N [2-[diphenylphosphanyl(phenyl)methyl]-3-methyl-1-phenyl-2-propan-2-ylbutyl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C=1C=CC=CC=1)C(C(C)C)(C(C)C)C(C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 ZJOSFSQAMSLVEL-UHFFFAOYSA-N 0.000 description 1
- HFKJQIJFRMRSKM-UHFFFAOYSA-N [3,5-bis(trifluoromethyl)phenoxy]boronic acid Chemical compound OB(O)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 HFKJQIJFRMRSKM-UHFFFAOYSA-N 0.000 description 1
- FKZWSMNNIQBSMA-UHFFFAOYSA-N [3-(1-diphenylphosphanylethyl)-3-ethyl-4-methylpentan-2-yl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(C(C)C)(CC)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 FKZWSMNNIQBSMA-UHFFFAOYSA-N 0.000 description 1
- URTZWVDSVDGQQT-UHFFFAOYSA-N [3-(1-diphenylphosphanylethyl)-3-methylhexan-2-yl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(C)(CCC)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 URTZWVDSVDGQQT-UHFFFAOYSA-N 0.000 description 1
- AMYQFNWEKFVBHX-UHFFFAOYSA-N [3-(1-diphenylphosphanylethyl)-3-propylhexan-2-yl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(CCC)(CCC)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 AMYQFNWEKFVBHX-UHFFFAOYSA-N 0.000 description 1
- JRJMHISKSJUQLS-UHFFFAOYSA-N [3-(1-diphenylphosphanylethyl)-4-methyl-3-propan-2-ylpentan-2-yl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(C(C)C)(C(C)C)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 JRJMHISKSJUQLS-UHFFFAOYSA-N 0.000 description 1
- RXXJANKNQAYDMQ-UHFFFAOYSA-N [3-(1-diphenylphosphanylethyl)-4-methylpentan-2-yl]-diphenylphosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)C(C)C(C(C)C)C(C)P(C=1C=CC=CC=1)C1=CC=CC=C1 RXXJANKNQAYDMQ-UHFFFAOYSA-N 0.000 description 1
- WUVAGGPQELVKAP-UHFFFAOYSA-N [3-[1-bis(3,5-diethylphenyl)phosphanylethyl]-3,4-dimethylpentan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C)C(C)(C(C)C)C(C)P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)=C1 WUVAGGPQELVKAP-UHFFFAOYSA-N 0.000 description 1
- WUGXLMDIKBFLJG-UHFFFAOYSA-N [3-[1-bis(3,5-diethylphenyl)phosphanylethyl]-3-ethylhexan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound C=1C(CC)=CC(CC)=CC=1P(C=1C=C(CC)C=C(CC)C=1)C(C)C(CC)(CCC)C(C)P(C=1C=C(CC)C=C(CC)C=1)C1=CC(CC)=CC(CC)=C1 WUGXLMDIKBFLJG-UHFFFAOYSA-N 0.000 description 1
- JFNXDLUQUIBUNS-UHFFFAOYSA-N [3-[1-bis(3,5-diethylphenyl)phosphanylethyl]-3-methylhexan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound C=1C(CC)=CC(CC)=CC=1P(C=1C=C(CC)C=C(CC)C=1)C(C)C(C)(CCC)C(C)P(C=1C=C(CC)C=C(CC)C=1)C1=CC(CC)=CC(CC)=C1 JFNXDLUQUIBUNS-UHFFFAOYSA-N 0.000 description 1
- OUZPDFLKHSOMFP-UHFFFAOYSA-N [3-[1-bis(3,5-diethylphenyl)phosphanylethyl]-3-propan-2-ylhexan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound C=1C(CC)=CC(CC)=CC=1P(C=1C=C(CC)C=C(CC)C=1)C(C)C(C(C)C)(CCC)C(C)P(C=1C=C(CC)C=C(CC)C=1)C1=CC(CC)=CC(CC)=C1 OUZPDFLKHSOMFP-UHFFFAOYSA-N 0.000 description 1
- ZIXANGRJMSVEPC-UHFFFAOYSA-N [3-[1-bis(3,5-diethylphenyl)phosphanylethyl]-4-methyl-3-propan-2-ylpentan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C)C(C(C)C)(C(C)C)C(C)P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)=C1 ZIXANGRJMSVEPC-UHFFFAOYSA-N 0.000 description 1
- PDXCCJCWCKWUNU-UHFFFAOYSA-N [3-[1-bis(3,5-diethylphenyl)phosphanylethyl]-4-methylpentan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C)C(C(C)C)C(C)P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)=C1 PDXCCJCWCKWUNU-UHFFFAOYSA-N 0.000 description 1
- ZSQRXNYKHKDZHC-UHFFFAOYSA-N [3-[1-bis(3,5-dimethylphenyl)phosphanylethyl]-3,4-dimethylpentan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(C)(C(C)C)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 ZSQRXNYKHKDZHC-UHFFFAOYSA-N 0.000 description 1
- BSWAPLLPHMTDJB-UHFFFAOYSA-N [3-[1-bis(3,5-dimethylphenyl)phosphanylethyl]-3-ethylhexan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(CC)(CCC)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 BSWAPLLPHMTDJB-UHFFFAOYSA-N 0.000 description 1
- CESWIDSGELLUFE-UHFFFAOYSA-N [3-[1-bis(3,5-dimethylphenyl)phosphanylethyl]-3-methylhexan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(C)(CCC)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 CESWIDSGELLUFE-UHFFFAOYSA-N 0.000 description 1
- NRLOMXOLORYOQR-UHFFFAOYSA-N [3-[1-bis(3,5-dimethylphenyl)phosphanylethyl]-3-propan-2-ylhexan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(C(C)C)(CCC)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 NRLOMXOLORYOQR-UHFFFAOYSA-N 0.000 description 1
- AYYBBEGCURNPKQ-UHFFFAOYSA-N [3-[1-bis(3,5-dimethylphenyl)phosphanylethyl]-3-propylhexan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(CCC)(CCC)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 AYYBBEGCURNPKQ-UHFFFAOYSA-N 0.000 description 1
- ULKOTZWMCCJINY-UHFFFAOYSA-N [3-[1-bis(3,5-dimethylphenyl)phosphanylethyl]-4-methyl-3-propan-2-ylpentan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(C(C)C)(C(C)C)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 ULKOTZWMCCJINY-UHFFFAOYSA-N 0.000 description 1
- AMVMENJBVIKCEB-UHFFFAOYSA-N [3-[1-bis(3,5-dimethylphenyl)phosphanylethyl]-4-methylpentan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(C(C)C)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 AMVMENJBVIKCEB-UHFFFAOYSA-N 0.000 description 1
- MBRMXTQNUJCEPN-UHFFFAOYSA-N [3-[1-bis(4-methoxy-3,5-dimethylphenyl)phosphanylethyl]-3,4-dimethylpentan-2-yl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C1=C(C)C(OC)=C(C)C=C1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)C(C)(C(C)C)C(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 MBRMXTQNUJCEPN-UHFFFAOYSA-N 0.000 description 1
- LJIFYOYZALRZMG-UHFFFAOYSA-N [3-[1-bis(4-methoxy-3,5-dimethylphenyl)phosphanylethyl]-3-ethyl-4-methylpentan-2-yl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)C(C(C)C)(CC)C(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 LJIFYOYZALRZMG-UHFFFAOYSA-N 0.000 description 1
- PNDWTSFHNQANMP-UHFFFAOYSA-N [3-[1-bis(4-methoxy-3,5-dimethylphenyl)phosphanylethyl]-3-ethylhexan-2-yl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)C(CC)(CCC)C(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 PNDWTSFHNQANMP-UHFFFAOYSA-N 0.000 description 1
- PMBTZRJBSGJHJI-UHFFFAOYSA-N [3-[1-bis(4-methoxy-3,5-dimethylphenyl)phosphanylethyl]-3-methylhexan-2-yl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)C(C)(CCC)C(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 PMBTZRJBSGJHJI-UHFFFAOYSA-N 0.000 description 1
- NWZILUHGIXDSDW-UHFFFAOYSA-N [3-[1-bis(4-methoxy-3,5-dimethylphenyl)phosphanylethyl]-3-propan-2-ylhexan-2-yl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)C(C(C)C)(CCC)C(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 NWZILUHGIXDSDW-UHFFFAOYSA-N 0.000 description 1
- OIEVHUZQBRGOEL-UHFFFAOYSA-N [3-[1-bis(4-methoxy-3,5-dimethylphenyl)phosphanylethyl]-3-propylhexan-2-yl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)C(CCC)(CCC)C(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 OIEVHUZQBRGOEL-UHFFFAOYSA-N 0.000 description 1
- KJCWYDMLQCHUEV-UHFFFAOYSA-N [3-[1-bis(4-methoxy-3,5-dimethylphenyl)phosphanylethyl]-4-methyl-3-propan-2-ylpentan-2-yl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C1=C(C)C(OC)=C(C)C=C1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)C(C(C)C)(C(C)C)C(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 KJCWYDMLQCHUEV-UHFFFAOYSA-N 0.000 description 1
- RDDDCQZAARFZND-UHFFFAOYSA-N [3-[1-bis(4-methoxy-3,5-dimethylphenyl)phosphanylethyl]-4-methylpentan-2-yl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C1=C(C)C(OC)=C(C)C=C1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)C(C(C)C)C(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 RDDDCQZAARFZND-UHFFFAOYSA-N 0.000 description 1
- APDQHTLFPNELDJ-UHFFFAOYSA-N [3-[1-bis(4-methylphenyl)phosphanylethyl]-3,4-dimethylpentan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(C)(C(C)C)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 APDQHTLFPNELDJ-UHFFFAOYSA-N 0.000 description 1
- CVSHORNWWRJEPR-UHFFFAOYSA-N [3-[1-bis(4-methylphenyl)phosphanylethyl]-3-ethyl-4-methylpentan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(C(C)C)(CC)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 CVSHORNWWRJEPR-UHFFFAOYSA-N 0.000 description 1
- PCRZTLCKNOCRMZ-UHFFFAOYSA-N [3-[1-bis(4-methylphenyl)phosphanylethyl]-3-ethylhexan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(CC)(CCC)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 PCRZTLCKNOCRMZ-UHFFFAOYSA-N 0.000 description 1
- XDFASWDXPGKZNV-UHFFFAOYSA-N [3-[1-bis(4-methylphenyl)phosphanylethyl]-3-methylhexan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(C)(CCC)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 XDFASWDXPGKZNV-UHFFFAOYSA-N 0.000 description 1
- XCWYZIXPSHNMRA-UHFFFAOYSA-N [3-[1-bis(4-methylphenyl)phosphanylethyl]-3-propan-2-ylhexan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(C(C)C)(CCC)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 XCWYZIXPSHNMRA-UHFFFAOYSA-N 0.000 description 1
- OBFIXLJMCPBDQE-UHFFFAOYSA-N [3-[1-bis(4-methylphenyl)phosphanylethyl]-3-propylhexan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(CCC)(CCC)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 OBFIXLJMCPBDQE-UHFFFAOYSA-N 0.000 description 1
- NOVMXOAQUKPIIW-UHFFFAOYSA-N [3-[1-bis(4-methylphenyl)phosphanylethyl]-4-methylpentan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(C(C)C)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 NOVMXOAQUKPIIW-UHFFFAOYSA-N 0.000 description 1
- XZGYGZZURXTNJM-UHFFFAOYSA-N [3-[1-bis(4-tert-butylphenyl)phosphanylethyl]-3,4-dimethylpentan-2-yl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C)C(C)(C(C)C)C(C)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 XZGYGZZURXTNJM-UHFFFAOYSA-N 0.000 description 1
- TXNDGPJAWIHTTG-UHFFFAOYSA-N [3-[1-bis(4-tert-butylphenyl)phosphanylethyl]-3-ethyl-4-methylpentan-2-yl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C)C(C(C)C)(CC)C(C)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 TXNDGPJAWIHTTG-UHFFFAOYSA-N 0.000 description 1
- VJFXOWVYVQQAIZ-UHFFFAOYSA-N [3-[1-bis(4-tert-butylphenyl)phosphanylethyl]-3-ethylhexan-2-yl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C)C(CC)(CCC)C(C)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 VJFXOWVYVQQAIZ-UHFFFAOYSA-N 0.000 description 1
- XQWLJAWTYMCZBZ-UHFFFAOYSA-N [3-[1-bis(4-tert-butylphenyl)phosphanylethyl]-3-propan-2-ylhexan-2-yl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C)C(C(C)C)(CCC)C(C)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 XQWLJAWTYMCZBZ-UHFFFAOYSA-N 0.000 description 1
- DLAUMGHYUATBOG-UHFFFAOYSA-N [3-bis(3,5-diethylphenyl)phosphanyl-2,2-dimethyl-1,3-diphenylpropyl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C=2C=CC=CC=2)C(C)(C)C(P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=CC=CC=2)C=2C=C(CC)C=C(CC)C=2)=C1 DLAUMGHYUATBOG-UHFFFAOYSA-N 0.000 description 1
- PFSFCBVARHQHDZ-UHFFFAOYSA-N [3-bis(3,5-diethylphenyl)phosphanyl-2-methyl-1,3-diphenylpropyl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C(C)C(P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=CC=CC=2)C=2C=CC=CC=2)C=2C=C(CC)C=C(CC)C=2)=C1 PFSFCBVARHQHDZ-UHFFFAOYSA-N 0.000 description 1
- VUDYQMOGQRVZHP-UHFFFAOYSA-N [3-bis(3,5-dimethylphenyl)phosphanyl-2,2-dimethyl-1,3-diphenylpropyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound CC1=CC(C)=CC(P(C(C=2C=CC=CC=2)C(C)(C)C(P(C=2C=C(C)C=C(C)C=2)C=2C=C(C)C=C(C)C=2)C=2C=CC=CC=2)C=2C=C(C)C=C(C)C=2)=C1 VUDYQMOGQRVZHP-UHFFFAOYSA-N 0.000 description 1
- UXHGOSLRMLRAKR-UHFFFAOYSA-N [3-bis(3,5-dimethylphenyl)phosphanyl-2-methyl-1,3-diphenylpropyl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C=1C=CC=CC=1)C(C)C(C=1C=CC=CC=1)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 UXHGOSLRMLRAKR-UHFFFAOYSA-N 0.000 description 1
- HHFRBVOBGKSABR-UHFFFAOYSA-N [3-bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-2,2-dimethyl-1,3-diphenylpropyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C1=C(C)C(OC)=C(C)C=C1P(C=1C=C(C)C(OC)=C(C)C=1)C(C(C)(C)C(P(C=1C=C(C)C(OC)=C(C)C=1)C=1C=C(C)C(OC)=C(C)C=1)C=1C=CC=CC=1)C1=CC=CC=C1 HHFRBVOBGKSABR-UHFFFAOYSA-N 0.000 description 1
- YBSSVZOWEVDNEX-UHFFFAOYSA-N [3-bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-2-methyl-1,3-diphenylpropyl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C1=C(C)C(OC)=C(C)C=C1P(C=1C=C(C)C(OC)=C(C)C=1)C(C=1C=CC=CC=1)C(C)C(C=1C=CC=CC=1)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 YBSSVZOWEVDNEX-UHFFFAOYSA-N 0.000 description 1
- GFGZHQCWZWATGF-UHFFFAOYSA-N [3-bis(4-methylphenyl)phosphanyl-1,3-diphenylpropyl]-bis(4-methylphenyl)phosphane Chemical compound C1=CC(C)=CC=C1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)CC(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 GFGZHQCWZWATGF-UHFFFAOYSA-N 0.000 description 1
- QSKODNPGIWZAFX-UHFFFAOYSA-N [3-bis(4-methylphenyl)phosphanyl-2,2-dimethyl-1,3-diphenylpropyl]-bis(4-methylphenyl)phosphane Chemical compound C1=CC(C)=CC=C1P(C=1C=CC(C)=CC=1)C(C(C)(C)C(P(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 QSKODNPGIWZAFX-UHFFFAOYSA-N 0.000 description 1
- RVNVDLRZOHJDCB-UHFFFAOYSA-N [3-bis(4-methylphenyl)phosphanyl-2-methyl-1,3-diphenylpropyl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C=1C=CC=CC=1)C(C)C(C=1C=CC=CC=1)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 RVNVDLRZOHJDCB-UHFFFAOYSA-N 0.000 description 1
- FAVPAJNZSCIJAV-UHFFFAOYSA-N [3-bis(4-tert-butylphenyl)phosphanyl-1,3-diphenylpropyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C1=CC(C(C)(C)C)=CC=C1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)CC(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 FAVPAJNZSCIJAV-UHFFFAOYSA-N 0.000 description 1
- RSUUHOWZZJHHAD-UHFFFAOYSA-N [3-bis(4-tert-butylphenyl)phosphanyl-2,2-dimethyl-1,3-diphenylpropyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(C)(C)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 RSUUHOWZZJHHAD-UHFFFAOYSA-N 0.000 description 1
- UJAIPJIQDBPNJR-UHFFFAOYSA-N [3-bis(4-tert-butylphenyl)phosphanyl-2-methyl-1,3-diphenylpropyl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C=1C=CC=CC=1)C(C)C(C=1C=CC=CC=1)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 UJAIPJIQDBPNJR-UHFFFAOYSA-N 0.000 description 1
- ZPOTWAMWTBMUMQ-UHFFFAOYSA-N [4-bis(3,5-diethylphenyl)phosphanyl-3,3-diethylpentan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C)C(CC)(CC)C(C)P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)=C1 ZPOTWAMWTBMUMQ-UHFFFAOYSA-N 0.000 description 1
- SIGKQAWQYVJJEN-UHFFFAOYSA-N [4-bis(3,5-diethylphenyl)phosphanyl-3,3-dimethylpentan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C)C(C)(C)C(C)P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)=C1 SIGKQAWQYVJJEN-UHFFFAOYSA-N 0.000 description 1
- KMBMCBSGQJKEAK-UHFFFAOYSA-N [4-bis(3,5-diethylphenyl)phosphanyl-3-ethyl-3-methylpentan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound CCC1=CC(CC)=CC(P(C(C)C(C)(CC)C(C)P(C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)C=2C=C(CC)C=C(CC)C=2)=C1 KMBMCBSGQJKEAK-UHFFFAOYSA-N 0.000 description 1
- HUNSYBJURFUMGS-UHFFFAOYSA-N [4-bis(3,5-diethylphenyl)phosphanyl-3-ethylpentan-2-yl]-bis(3,5-diethylphenyl)phosphane Chemical compound C=1C(CC)=CC(CC)=CC=1P(C=1C=C(CC)C=C(CC)C=1)C(C)C(CC)C(C)P(C=1C=C(CC)C=C(CC)C=1)C1=CC(CC)=CC(CC)=C1 HUNSYBJURFUMGS-UHFFFAOYSA-N 0.000 description 1
- AVXOESWKKURTML-UHFFFAOYSA-N [4-bis(3,5-dimethylphenyl)phosphanyl-3,3-diethylpentan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(CC)(CC)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 AVXOESWKKURTML-UHFFFAOYSA-N 0.000 description 1
- JVSIHODQUUVXLH-UHFFFAOYSA-N [4-bis(3,5-dimethylphenyl)phosphanyl-3,3-dimethylpentan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(C)(C)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 JVSIHODQUUVXLH-UHFFFAOYSA-N 0.000 description 1
- ZZVWGSFRGNXCDV-UHFFFAOYSA-N [4-bis(3,5-dimethylphenyl)phosphanyl-3-ethyl-3-methylpentan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(C)(CC)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 ZZVWGSFRGNXCDV-UHFFFAOYSA-N 0.000 description 1
- ZILHQDGTNMEODM-UHFFFAOYSA-N [4-bis(3,5-dimethylphenyl)phosphanyl-3-ethylpentan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(CC)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 ZILHQDGTNMEODM-UHFFFAOYSA-N 0.000 description 1
- YOHVTQHWOPUYGB-UHFFFAOYSA-N [4-bis(3,5-dimethylphenyl)phosphanyl-3-methylpentan-2-yl]-bis(3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=CC(C)=CC=1P(C=1C=C(C)C=C(C)C=1)C(C)C(C)C(C)P(C=1C=C(C)C=C(C)C=1)C1=CC(C)=CC(C)=C1 YOHVTQHWOPUYGB-UHFFFAOYSA-N 0.000 description 1
- NOYFZSXHIQYDLH-UHFFFAOYSA-N [4-bis(4-methoxy-3,5-dimethylphenyl)phosphanyl-3-ethyl-3-methylpentan-2-yl]-bis(4-methoxy-3,5-dimethylphenyl)phosphane Chemical compound C=1C(C)=C(OC)C(C)=CC=1P(C=1C=C(C)C(OC)=C(C)C=1)C(C)C(C)(CC)C(C)P(C=1C=C(C)C(OC)=C(C)C=1)C1=CC(C)=C(OC)C(C)=C1 NOYFZSXHIQYDLH-UHFFFAOYSA-N 0.000 description 1
- KNVSHMGKPBFOIS-UHFFFAOYSA-N [4-bis(4-methylphenyl)phosphanyl-3,3-dimethylpentan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(C)(C)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 KNVSHMGKPBFOIS-UHFFFAOYSA-N 0.000 description 1
- NIMLQPWOYIZMGR-UHFFFAOYSA-N [4-bis(4-methylphenyl)phosphanyl-3-ethyl-3-methylpentan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(C)(CC)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 NIMLQPWOYIZMGR-UHFFFAOYSA-N 0.000 description 1
- OYMKXLXREBNETC-UHFFFAOYSA-N [4-bis(4-methylphenyl)phosphanyl-3-ethylpentan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(CC)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 OYMKXLXREBNETC-UHFFFAOYSA-N 0.000 description 1
- LVYGXVVRZGNPMS-UHFFFAOYSA-N [4-bis(4-methylphenyl)phosphanyl-3-methylpentan-2-yl]-bis(4-methylphenyl)phosphane Chemical compound C=1C=C(C)C=CC=1P(C=1C=CC(C)=CC=1)C(C)C(C)C(C)P(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 LVYGXVVRZGNPMS-UHFFFAOYSA-N 0.000 description 1
- RZOURTMYDUKHBD-UHFFFAOYSA-N [4-bis(4-tert-butylphenyl)phosphanyl-3,3-diethylpentan-2-yl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C)C(CC)(CC)C(C)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 RZOURTMYDUKHBD-UHFFFAOYSA-N 0.000 description 1
- QAVQMCMRCVLIPZ-UHFFFAOYSA-N [4-bis(4-tert-butylphenyl)phosphanyl-3,3-dimethylpentan-2-yl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C)C(C)(C)C(C)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 QAVQMCMRCVLIPZ-UHFFFAOYSA-N 0.000 description 1
- GJXPZRFKNDZWJQ-UHFFFAOYSA-N [4-bis(4-tert-butylphenyl)phosphanyl-3-ethylpentan-2-yl]-bis(4-tert-butylphenyl)phosphane Chemical compound C=1C=C(C(C)(C)C)C=CC=1P(C=1C=CC(=CC=1)C(C)(C)C)C(C)C(CC)C(C)P(C=1C=CC(=CC=1)C(C)(C)C)C1=CC=C(C(C)(C)C)C=C1 GJXPZRFKNDZWJQ-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 description 1
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- HFJCAPWHVJSXPY-UHFFFAOYSA-N bis(3,5-diethylphenyl)-(3-methylpentyl)phosphane Chemical compound C(C)C=1C=C(C=C(C=1)CC)P(C1=CC(=CC(=C1)CC)CC)CCC(CC)C HFJCAPWHVJSXPY-UHFFFAOYSA-N 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- PESYEWKSBIWTAK-UHFFFAOYSA-N cyclopenta-1,3-diene;titanium(2+) Chemical compound [Ti+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 PESYEWKSBIWTAK-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- KUMNEOGIHFCNQW-UHFFFAOYSA-N diphenyl phosphite Chemical compound C=1C=CC=CC=1OP([O-])OC1=CC=CC=C1 KUMNEOGIHFCNQW-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- WUOIAOOSKMHJOV-UHFFFAOYSA-N ethyl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(CC)C1=CC=CC=C1 WUOIAOOSKMHJOV-UHFFFAOYSA-N 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000001207 fluorophenyl group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-M isovalerate Chemical compound CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- OEDXASUOCKHCRL-UHFFFAOYSA-N n',n'-dimethyl-1,2-diphenylethane-1,2-diamine Chemical compound C=1C=CC=CC=1C(N(C)C)C(N)C1=CC=CC=C1 OEDXASUOCKHCRL-UHFFFAOYSA-N 0.000 description 1
- NVCTWTUCFNBXHB-UHFFFAOYSA-N n'-methyl-1,2-diphenylethane-1,2-diamine Chemical compound C=1C=CC=CC=1C(NC)C(N)C1=CC=CC=C1 NVCTWTUCFNBXHB-UHFFFAOYSA-N 0.000 description 1
- BTHYVQUNQHWNLS-UHFFFAOYSA-N n,n'-dimethyl-1,2-diphenylethane-1,2-diamine Chemical compound C=1C=CC=CC=1C(NC)C(NC)C1=CC=CC=C1 BTHYVQUNQHWNLS-UHFFFAOYSA-N 0.000 description 1
- ZYZHMSJNPCYUTB-UHFFFAOYSA-N n-benzyl-1-phenylethanamine Chemical compound C=1C=CC=CC=1C(C)NCC1=CC=CC=C1 ZYZHMSJNPCYUTB-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- PARWUHTVGZSQPD-UHFFFAOYSA-N phenylsilane Chemical compound [SiH3]C1=CC=CC=C1 PARWUHTVGZSQPD-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003303 ruthenium Chemical class 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/68—Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
- C07C209/70—Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton by reduction of unsaturated amines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/44—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers
- C07C209/52—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers by reduction of imines or imino-ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C269/06—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups by reactions not involving the formation of carbamate groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
-
- 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
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0046—Ruthenium compounds
- C07F15/0053—Ruthenium compounds without a metal-carbon linkage
-
- 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
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pyridine Compounds (AREA)
- Catalysts (AREA)
Description
前述の如く、従来の水素化触媒では、その触媒活性は低く、エナンチオ選択性も十分ではなかった。
[1] 一般式(1)
RuXYAB (1)
(XおよびYは、互いに独立して、水素またはアニオン性基であり、Aは、一般式(2)
R5、R6、R7およびR8は、互いに独立して、置換基を有していてもよい炭素数1〜30の炭化水素基であり、
Wは、置換基を有していてもよい、炭素数1または2の炭化水素基あるいは単結合である。)
で表されるジホスフィン化合物であり、Bは、一般式(3)
R13、R14、R15およびR16は、互いに独立して、水素、あるいは置換基を有していてもよい、鎖状または環状である炭素数1〜30の炭化水素基であり、
Zは、置換基を有していてもよい、鎖状もしくは環状である炭素数1〜10の炭化水素基または単結合である。)
で表されるジアミン化合物であり、ルテニウムの各配位子はどのように配位されていてもよい。)
で表されるルテニウム錯体と一般式(4)
R19は、水素、あるいは置換基を有していてもよい、アルキル基、アルケニル基、アルキニル基、シクロアルキル基、シクロアルケニル基、アリール基、ヘテロアリール基、アラルキル基またはヘテロアラルキル基であり、
またR17、R18およびR19の内の二つが一緒になって置換基を有していてもよい環を形成していてもよい。)
で表されるイミン化合物、および
アルカリ金属またはアルカリ土類金属の塩、四級アンモニウム塩および三級アミンからなる群から選択される1種または2種以上の塩基を、非プロトン性溶媒中または無溶媒にて、加圧水素下で混合して前記イミン化合物を水素化することを特徴とする、一般式(5)
で表される光学活性アミン化合物の製造方法。
RuXYALn (6)
(Lは有機配位子であり、nは、0〜2の間の任意の数であり、X、YおよびAは、[1]で定義したとおりである。)
で表されるルテニウム錯体、一般式(3)
で表されるジアミン化合物と一般式(4)
で表されるイミン化合物、および
アルカリ金属またはアルカリ土類金属の塩、四級アンモニウム塩および三級アミンからなる群から選択される1種または2種以上の塩基を、非プロトン性溶媒中または無溶媒にて、加圧水素下で混合して前記イミン化合物を水素化することを特徴とする、一般式(5)
で表される光学活性アミン化合物の製造方法。
本発明の方法に用いるルテニウム錯体は、イミン化合物を光学活性アミン化合物に水素化できるものであれば特に限定されないが、典型的には、一般式(1)で表される。
RuXYAB (1)
上記XおよびYとしては、例えば、水素、フッ素原子、塩素原子、臭素原子、ヨウ素原子、アセトキシ基、ベンゾイルオキシ基、(2,6−ジヒドロキシベンゾイル)オキシ基、(2,5−ジヒドロキシベンゾイル)オキシ基、(3−アミノベンゾイル)オキシ基、(2,6−メトキシベンゾイル)オキシ基、(2,4,6−トリイソプロピルベンゾイル)オキシ基、1−ナフタレンカルボニルオキシ基、2−ナフタレンカルボニルオキシ基、トリフルオロアセトキシ基、トリフルオロメタンスルホキシ基、テトラヒドロボラートアニオン、テトラフルオロボラートアニオンおよびテトラキス[3,5−ビス(トリフルオロメチル)フェニル]ボラートアニオンなどが挙げられる。好ましくは、触媒活性および錯体の安定性の観点から、水素、フッ素原子、塩素原子、臭素原子、ヨウ素原子などのハロゲン原子、テトラヒドロボラートアニオン、テトラフルオロボラートアニオンであり、特に好ましくは、水素、塩素原子、臭素原子、ヨウ素原子およびテトラヒドロボラートアニオンである。
XおよびYの組み合わせとしては、好ましくは、触媒活性および錯体の安定性の観点から、Xが水素、塩素原子、臭素原子およびヨウ素原子からなる群から選択される1種であり、Yが塩素原子、臭素原子、ヨウ素原子およびテトラヒドロボラートアニオンからなる群から選択される1種である組み合わせである。
上記炭化水素基は、さらに、アルキル基、アルケニル基、アルキニル基、シクロアルキル基、シクロアルケニル基、アリール基、ヘテロアリール基、アルコキシ基、エステル基、アシルオキシ基、ハロゲン原子、ニトロ基、シアノ基、パーフルオロアルキル基などの許容される各種の置換基を有していてもよい。
R5、R6、R7およびR8の組み合わせとしては、好ましくは、触媒活性およびエナンチオ選択性の観点から、全てのR5〜R8がフェニル基または置換基を有するフェニル基である組み合わせであって、より好ましくは、フェニル基またはアルキル基もしくはアルコキシ基を有するフェニル基である組み合わせである。
上記アルケニル基としては、例えば、ビニル基、1−プロペニル基、アリル基、イソプロペニル基、1−ブテニル基、クロチル基、3−ブテニル基、イソブテニル基、メタリル基および2−フェニルビニル基などが挙げられる。
上記アルキニル基としては、例えば、エチニル基、1−プロピニル基、プロパルギル基、1−ブチニル基、2−ブチニル基、3−ブチニル基、3−メチル−1−ブチニル基および2−フェニルエチニル基などが挙げられる。
上記シクロアルケニル基としては、例えば、シクロプロペニル基、シクロブテニル基、シクロペンテニル基およびシクロヘキセニル基などが挙げられる。
上記アリール基としては、例えば、フェニル基、トリル基、キシリル基、フェロセニル基およびナフチル基などが挙げられる。
上記ヘテロアリール基としては、例えばピリジル基、ピリミジル基、ピラジル基、キノリル基、イソキノリル基、チエニル基、フリル基、ピロリル基、インドリル基、イミダゾリル基、ピラゾリル基、チアゾリル基およびトリアゾリル基などが挙げられる。
上記エステル基としては、例えば、メトキシカルボニル基、エトキシカルボニル基、ブトキシカルボニル基およびベンジルオキシカルボニル基などが挙げられる。
上記アシルオキシ基としては、例えば、アセトキシ基、トリフルオロアセトキシ基、アクリロキシ基およびメタクリロキシ基などが挙げられる。
上記ハロゲン原子としては、例えば、フッ素原子、塩素原子、臭素原子およびヨウ素原子などが挙げられる。
上記パーフルオロアルキル基としては、例えば、トリフルオロメチル基およびペンタフルオロエチル基などが挙げられる。
上記置換基を有していてもよい、炭素数1または2の炭化水素基としては、メチレン基、エチレン基およびビニレン基などが挙げられる。好ましくは、触媒活性とエナンチオ選択性の観点から、無置換のメチレン基である。
2位、4位にジフェニルホスフィノ基を有するペンタン誘導体としては、SKEWPHOS:2,4−ビス(ジフェニルホスフィノ)ペンタン、2,4−ビス(ジフェニルホスフィノ)−3−メチルペンタン、2,4−ビス(ジフェニルホスフィノ)−3,3−ジメチルペンタン、2,4−ビス(ジフェニルホスフィノ)−3−エチルペンタン、2,4−ビス(ジフェニルホスフィノ)−3,3−ジエチルペンタン、2,4−ビス(ジフェニルホスフィノ)−3−プロピルペンタン、2,4−ビス(ジフェニルホスフィノ)−3,3−ジプロピルペンタン、2,4−ビス(ジフェニルホスフィノ)−3−イソプロピルペンタン、2,4−ビス(ジフェニルホスフィノ)−3,3−ジイソプロピルペンタン、2,4−ビス(ジフェニルホスフィノ)−3−エチル−3−メチルペンタン、2,4−ビス(ジフェニルホスフィノ)−3−メチル−3−プロピルペンタン、2,4−ビス(ジフェニルホスフィノ)−3−メチル−3−イソプロピルペンタン、2,4−ビス(ジフェニルホスフィノ)−3−エチル−3−プロピルペンタン、2,4−ビス(ジフェニルホスフィノ)−3−エチル−3−イソプロピルペンタン、2,4−ビス(ジフェニルホスフィノ)−3−プロピル−3−イソプロピルペンタンなどが挙げられる。
R13、R14、R15およびR16は、互いに独立して、特に限定されないが、例えば、水素ならびに脂肪族または脂環族の飽和または不飽和の炭化水素基、単環または多環の芳香族または芳香脂肪族の炭化水素基などが挙げられ、前記炭化水素基はさらに置換基を有していてもよい。
上記炭化水素基は、さらに、アルキル基、アルケニル基、アルキニル基、シクロアルキル基、シクロアルケニル基、アリール基、ヘテロアリール基、アルコキシ基、エステル基、アシルオキシ基、ハロゲン原子、ニトロ基、シアノ基、パーフルオロアルキル基など置換基を有していてもよい。
上記アルケニル基としては、例えば、ビニル基、1−プロペニル基、アリル基、イソプロペニル基、1−ブテニル基、クロチル基、3−ブテニル基、イソブテニル基、メタリル基および2−フェニルビニル基などが挙げられる。
上記アルキニル基としては、例えば、エチニル基、1−プロピニル基、プロパルギル基、1−ブチニル基、2−ブチニル基、3−ブチニル基、3−メチル−1−ブチニル基および2−フェニルエチニル基などが挙げられる。
上記シクロアルケニル基としては、例えば、シクロプロペニル基、シクロブテニル基、シクロペンテニル基およびシクロヘキセニル基などが挙げられる。
上記アリール基としては、例えば、フェニル基、トリル基、キシリル基、フェロセニル基およびナフチル基などが挙げられる。
上記ヘテロアリール基としては、例えばピリジル基、ピリミジル基、ピラジル基、キノリル基、イソキノリル基、チエニル基、フリル基、ピロリル基、インドリル基、イミダゾリル基、ピラゾリル基、チアゾリル基およびトリアゾリル基などが挙げられる。
上記エステル基としては、例えば、メトキシカルボニル基、エトキシカルボニル基、ブトキシカルボニル基およびベンジルオキシカルボニル基などが挙げられる。
上記アシルオキシ基としては、例えば、アセトキシ基、トリフルオロアセトキシ基、アクリロキシ基およびメタクリロキシ基などが挙げられる。
上記ハロゲン原子としては、例えば、フッ素原子、塩素原子、臭素原子およびヨウ素原子などが挙げられる。
上記パーフルオロアルキル基としては、例えば、トリフルオロメチル基およびペンタフルオロエチル基などが挙げられる。
上記置換基を有していてもよい炭素数1〜10の炭化水素基としては、メチレン基、エチレン基およびプロピレン基などが挙げられる。
上記置換基を有していてもよい炭素数1〜10の炭化水素基は、さらに、アルキル基、アルケニル基、アルキニル基、シクロアルキル基、シクロアルケニル基、アリール基、ヘテロアリール基、アルコキシ基、エステル基、アシルオキシ基、ハロゲン原子、ニトロ基、シアノ基、パーフルオロアルキル基など置換基を有していてもよい。
上記アルケニル基としては、例えば、ビニル基、1−プロペニル基、アリル基、イソプロペニル基、1−ブテニル基、クロチル基、3−ブテニル基、イソブテニル基、メタリル基および2−フェニルビニル基などが挙げられる。
上記アルキニル基としては、例えば、エチニル基、1−プロピニル基、プロパルギル基、1−ブチニル基、2−ブチニル基、3−ブチニル基、3−メチル−1−ブチニル基および2−フェニルエチニル基などが挙げられる。
上記シクロアルケニル基としては、例えば、シクロプロペニル基、シクロブテニル基、シクロペンテニル基およびシクロヘキセニル基などが挙げられる。
上記アリール基としては、例えば、フェニル基、トリル基、キシリル基、フェロセニル基およびナフチル基などが挙げられる。
上記エステル基としては、例えば、メトキシカルボニル基、エトキシカルボニル基、ブトキシカルボニル基およびベンジルオキシカルボニル基などが挙げられる。
上記アシルオキシ基としては、例えば、アセトキシ基、トリフルオロアセトキシ基、アクリロキシ基およびメタクリロキシ基などが挙げられる。
上記ハロゲン原子としては、例えば、フッ素原子、塩素原子、臭素原子およびヨウ素原子などが挙げられる。
上記パーフルオロアルキル基としては、例えば、トリフルオロメチル基およびペンタフルオロエチル基などが挙げられる。
一般式(1)および(6)で表されるルテニウム錯体の合成方法は、特許第3566955号公報および特開2004−238306号公報などに記載されている。具体的には、ジホスフィン化合物と原料であるルテニウム錯体との反応により一般式(6)で表されるルテニウム錯体を合成できる。さらに、一般式(6)で表されるルテニウム錯体とジアミン化合物とを反応させることにより一般式(1)で表されるルテニウム錯体を合成することが可能である。
上記アルケニル基としては、例えば、ビニル基、1−プロペニル基、アリル基、イソプロペニル基、1−ブテニル基、クロチル基、3−ブテニル基、イソブテニル基、メタリル基および2−フェニルビニル基などが挙げられる。
上記アルキニル基としては、例えば、エチニル基、1−プロピニル基、プロパルギル基、1−ブチニル基、2−ブチニル基、3−ブチニル基、3−メチル−1−ブチニル基および2−フェニルエチニル基などが挙げられる。
上記シクロアルケニル基としては、例えば、シクロプロペニル基、シクロブテニル基、シクロペンテニル基およびシクロヘキセニル基などが挙げられる。
上記アリール基としては、例えば、フェニル基、トリル基、キシリル基、フェロセニル基およびナフチル基などが挙げられる。
上記エステル基としては、例えば、メトキシカルボニル基、エトキシカルボニル基、ブトキシカルボニル基およびベンジルオキシカルボニル基などが挙げられる。
上記アシルオキシ基としては、例えば、アセトキシ基、トリフルオロアセトキシ基、アクリロキシ基およびメタクリロキシ基などが挙げられる。
上記ハロゲン原子としては、例えば、フッ素原子、塩素原子、臭素原子およびヨウ素原子などが挙げられる。
上記パーフルオロアルキル基としては、例えば、トリフルオロメチル基およびペンタフルオロエチル基などが挙げられる。
本発明におけるイミン化合物の水素化反応は、反応形式が、バッチ式または連続式のいずれにおいても実施することができる。
下記の実施例において、反応はすべてアルゴンガスまたは窒素ガスなどの不活性ガス雰囲気下にて行った。また、NMRは、ECX−400P(400MHz,日本電子社製)を用いて測定した。1HNMR、13CNMRはテトラメチルシランを内部標準物質に用い、その信号をδ=0(δは化学シフト)とした。光学純度は高速液体クロマトグラフィー(HPLC)により,CHIRALCEL OD−H(0.46cm×25cm)、CHIRALCEL OJ−H(0.46cm×25cm)、CHIRALPAK IA(0.46cm×25cm)(ダイセル社製)を用いて測定した。比旋光度はP−2200(日本分光社製)を用いて測定した。
N−(1−フェニルエチリデン)−2−メトキシアニリンの不斉水素化による(R)−N−(2−メトキシフェニル)−1−フェニルエチルアミンの合成
N−(1−フェニルエチリデン)−2−メトキシアニリンの不斉水素化による(R)−N−(2−メトキシフェニル)−1−フェニルエチルアミンの合成
ルテニウム錯体、S/C、反応時間を変えた以外は実施例1と同じ条件で反応を実施し、(R)−N−(2−メトキシフェニル)−1−フェニルエチルアミンを合成した。結果を表1にまとめて示す。
溶媒、S/C、基質濃度、塩基濃度、反応時間を変えた以外は実施例1と同じ条件で反応を実施し、(R)−N−(2−メトキシフェニル)−1−フェニルエチルアミンを合成した。結果を表2にまとめて示す。
N−[1−(3−クロロフェニル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(3−クロロフェニル)エチルアミンの合成
N−(1−フェニルエチリデン)−4−メトキシアニリンの不斉水素化による(R)−N−(4−メトキシフェニル)−1−フェニルエチルアミンの合成
N−(1−フェニルエチリデン)−4−メトキシアニリンの不斉水素化による(R)−N−(4−メトキシフェニル)−1−フェニルエチルアミンの合成
N−(1−フェニルエチリデン)アニリンの不斉水素化による(R)−N−フェニル−1−フェニルエチルアミンの合成
N−(1−フェニルエチリデン)−3−メチルアニリンの不斉水素化による(+)−N−(3−メチルフェニル)−1−フェニルエチルアミンの合成
N−(1−フェニルエチリデン)−4−ブロモアニリンの不斉水素化による(R)−N−(4−ブロモフェニル)−1−フェニルエチルアミンの合成
N−(1−フェニルエチリデン)ブチルアミンの不斉水素化による(+)−N−ブチル−1−フェニルエチルアミンの合成
得られた(+)−N−ブチル−1−フェニルエチルアミンを無水酢酸と反応させ、N−アセチル−N−ブチル−1−フェニルエチルアミンへと誘導した後、HPLCより光学純度は97%eeであった。HPLC(カラム、CHIRALPAK IA;溶媒、ヘキサン/2−プロパノール=95/5;流量、1.0mL/min;温度、30℃;UV波長、210nm;N−アセチル−N−ブチル−1−フェニルエチルアミンのtR、8.2分、9.1分)。
N−[1−(4−メチルフェニル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(4−メチルフェニル)エチルアミンの合成
N−[1−(4−メトキシフェニル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(4−メトキシフェニル)エチルアミンの合成
N−[1−(3−クロロフェニル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(3−クロロフェニル)エチルアミンの合成
N−[1−(4−クロロフェニル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(4−クロロフェニル)エチルアミンの合成
N−[1−(2−フルオロフェニル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(2−フルオロフェニル)エチルアミンの合成
N−[1−(4−フルオロフェニル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(4−フルオロフェニル)エチルアミンの合成
N−[1−(4−トリフルオロメチルフェニル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(4−トリフルオロメチルフェニル)エチルアミンの合成
N−[1−(2−ナフチル)エチリデン]−2−メトキシアニリンの不斉水素化による(R)−N−(2−メトキシフェニル)−1−(2−ナフチル)エチルアミンの合成
N−[1−(3−ピリジル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(3−ピリジル)エチルアミンの合成
N−[1−(4−ピリジル)エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−(4−ピリジル)エチルアミンの合成
N−(1−フェニルプロピリデン)−2−メトキシアニリンの不斉水素化による(R)−N−(2−メトキシフェニル)−1−フェニルプロピルアミンの合成
N−[1−[3−[N’−(2−メトキシフェニル)イミノエチル]フェニル]エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−[3−[N’−(2−メトキシフェニル)アミノエチル]フェニル]エチルアミンの合成
N−[1−[3−[N’−(2−メトキシフェニル)イミノエチル]フェニル]エチリデン]−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−1−[3−[N’−(2−メトキシフェニル)アミノエチル]フェニル]エチルアミンの合成
N−[1−(4−クロロ−3−メチルフェニル)エチリデン]−3−ブロモアニリンの不斉水素化による(+)−N−(3−ブロモフェニル)−1−(4−クロロ−3−メチルフェニル)エチルアミンの合成
N−[1−(4−クロロフェニル)エチリデン]−4−(N’−Boc−N’−メチルアミノ)アニリンの不斉水素化による(+)−N−[4−(N’−Boc−N’−メチルアミノ)フェニル]−1−(4−クロロフェニル)エチルアミンの合成
N−[1−(4−クロロフェニル)エチリデン]−4−(N’−Boc−N’−メチルアミノ)アニリンの不斉水素化による(+)−N−[4−(N’−Boc−N’−メチルアミノ)フェニル]−1−(4−クロロフェニル)エチルアミンの合成
N−(1−インダニリデン)−3,4,5−トリメトキシアニリンの不斉水素化による1−[N−(3,4,5−トリメトキシフェニル)]アミノインダンの合成
N−(1−インダニリデン)−3,4,5−トリメトキシアニリンの不斉水素化による1−[N−(3,4,5−トリメトキシフェニル)]アミノインダンの合成
N−(1−インダニリデン)−3,4−ジメトキシアニリンの不斉水素化による1−[N−(3,4−ジメトキシフェニル)]アミノインダンの合成
様々なRu錯体を用いて反応を実施し、1−[N−(3,4−ジメトキシフェニル)]アミノインダンを合成した。結果を表4にまとめて示す。
N−(4−メチル−3−ペンテン−2−イリデン)−2−メトキシアニリンの不斉水素化による(−)−N−(2−メトキシフェニル)−4−メチル−3−ペンテン−2−イルアミンの合成
RuH(BH4)[(S,S)−xylskewphos][(S,S)−dpen]錯体の合成
ルテニウム錯体、S/C、反応時間を変えた以外は実施例1と同じ条件で反応を実施し、(R)−N−(2−メトキシフェニル)−1−フェニルエチルアミンを合成した。結果を表5にまとめて示す。
N−(1−フェニルエチリデン)ベンジルアミンの不斉水素化による(R)−N−ベンジル−1−フェニルエチルアミンの合成
N−(1−フェニルエチリデン)−4−メトキシアニリンの不斉水素化による(S)−N−(4−メトキシフェニル)−1−フェニルエチルアミンの合成
N−(1−フェニルエチリデン)−2−メトキシアニリンの不斉水素化反応
Ru錯体をRuCl2[(R)−1−[(S)−2−(ジシクロヘキシルホスフィノ)フェロセニル]エチルジフェニルホスフィン][(R,R)−dpen]に変えた以外は比較例2と同じ条件で反応を実施したが、反応は全く進行しなかった。
N−(1−フェニルエチリデン)−2−メトキシアニリンの不斉水素化反応
Claims (6)
- 一般式(1)
RuXYAB (1)
(XおよびYは、互いに独立して、水素またはアニオン性基であり、Aは、一般式(2)
R5、R6、R7およびR8は、互いに独立して、置換基を有していてもよい炭素数1〜30の炭化水素基であり、
Wは、置換基を有していてもよい、炭素数1または2の炭化水素基あるいは単結合である。)
で表されるジホスフィン化合物であり、Bは、一般式(3)
R13およびR15が水素であり、R14が水素、フェニル基または置換フェニル基であり、R16がフェニル基または置換フェニル基であり、
Zは、置換基を有していてもよい、鎖状もしくは環状である炭素数1〜10の炭化水素基または単結合である。)
で表されるジアミン化合物であり、ルテニウムの各配位子はどのように配位されていてもよい。)
で表されるルテニウム錯体と一般式(4)
R19は、水素、あるいは置換基を有していてもよい、アルキル基、アルケニル基、アルキニル基、シクロアルキル基、シクロアルケニル基、アリール基、ヘテロアリール基、アラルキル基またはヘテロアラルキル基であり、
またR17、R18およびR19の内の二つが一緒になって置換基を有していてもよい環を形成していてもよい。)
で表されるイミン化合物、および
アルカリ金属またはアルカリ土類金属の塩、四級アンモニウム塩および三級アミンからなる群から選択される1種または2種以上の塩基を、非プロトン性溶媒中にて、加圧水素下で混合して前記イミン化合物を水素化することを特徴とする、一般式(5)
で表される光学活性アミン化合物の製造方法。 - 一般式(1)中、Aが、SKEWPHOS:2,4−ビス(ジフェニルホスフィノ)ペンタン、TolSKEWPHOS:2,4−ビス(ジ−4−トリルホスフィノ)ペンタン、XylSKEWPHOS:2,4−ビス(ジ−3,5−キシリルホスフィノ)ペンタンまたはModSKEWPHOS:2,4−ビス[ビス(3,5−ジメチル−4−メトキシフェニル)ホスフィノ]ペンタンである、請求項1に記載の製造方法。
- 一般式(3)中、R9、R10、R11、R12、R13およびR15が水素であり、R14が水素、フェニル基、4−トリフルオロメチルフェニル基、4−フルオロフェニル基、4−メトキシフェニル基または3−メトキシフェニル基であり、R16が、フェニル基、4−トリフルオロメチルフェニル基、4−フルオロフェニル基、4−メトキシフェニル基または3−メトキシフェニル基であり、Zが単結合である、請求項1または2に記載の製造方法。
- 非プロトン性溶媒が、トルエン、ベンゼン、テトラヒドロフランおよびtert−ブチルメチルエーテルからなる群から選択される1種または2種以上である、請求項1〜3のいずれか一項に記載の製造方法。
- 一般式(4)中、R17が、置換基を有していてもよい、アルケニル基、アルキニル基、シクロアルケニル基、アリール基またはヘテロアリール基であり、R18が、R17と異なって、置換基を有していてもよい、アルキル基、シクロアルキル基、アルケニル基、シクロアルケニル基またはアリール基であり、またR17およびR18が一緒になって置換基を有していてもよい環を形成していてもよく、R19が、置換基を有していてもよい、アルキル基、アルケニル基、アルキニル基、アリール基、ヘテロアリール基またはアラルキル基である、請求項1〜4のいずれか一項に記載の製造方法。
- 一般式(4)中、R17が置換基を有していてもよい、アルケニル基、アリール基またはヘテロアリール基であり、R18が、置換基を有していてもよいアルキル基またはシクロアルキル基であり、またR17およびR18が一緒になって置換基を有していてもよい環を形成していてもよく、R19が、置換基を有していてもよい、アルキル基、アリール基またはアラルキル基である、請求項1〜4のいずれか一項に記載の製造方法。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2013017845A JP6173702B2 (ja) | 2012-02-01 | 2013-01-31 | 光学活性アミン化合物の製造方法 |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2012019742 | 2012-02-01 | ||
JP2012019742 | 2012-02-01 | ||
JP2013017845A JP6173702B2 (ja) | 2012-02-01 | 2013-01-31 | 光学活性アミン化合物の製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013177374A JP2013177374A (ja) | 2013-09-09 |
JP6173702B2 true JP6173702B2 (ja) | 2017-08-02 |
Family
ID=47631354
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013017845A Active JP6173702B2 (ja) | 2012-02-01 | 2013-01-31 | 光学活性アミン化合物の製造方法 |
Country Status (3)
Country | Link |
---|---|
US (1) | US20130197234A1 (ja) |
EP (1) | EP2623509A1 (ja) |
JP (1) | JP6173702B2 (ja) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11498901B2 (en) * | 2018-03-02 | 2022-11-15 | Firmenich Sa | Hydrogenation of imines with Ru complexes |
US20220162181A1 (en) | 2019-08-08 | 2022-05-26 | Firmenich Sa | Hydrogenation of imines with ru complexes |
CN114262252B (zh) * | 2021-11-09 | 2024-01-23 | 云南民族大学 | 一种以季铵盐催化炔烃制备烯烃和烷烃的方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2731377B2 (ja) * | 1994-12-07 | 1998-03-25 | 科学技術振興事業団 | 光学活性アルコール類の製造方法 |
EP1299401B1 (en) * | 2000-06-02 | 2004-03-31 | Chirotech Technology Limited | Chiral ligands for asymmetric catalysis |
JP2004504371A (ja) * | 2000-07-24 | 2004-02-12 | カイロテック・テクノロジー・リミテッド | ルテニウム錯体および不斉水素化におけるその使用 |
JP3566955B2 (ja) * | 2001-12-28 | 2004-09-15 | 関東化学株式会社 | 新規ルテニウム錯体およびこれを触媒として用いるアルコール化合物の製造方法 |
JP2005525426A (ja) * | 2002-05-15 | 2005-08-25 | カマルディン アブドゥール−ラシッド | ルテニウム錯体を触媒として用いた不活性イミンの水素添加法 |
JP2004238306A (ja) | 2003-02-04 | 2004-08-26 | Nagoya Industrial Science Research Inst | ルテニウムヒドリド錯体、アルコール化合物の製造方法およびラセミ体カルボニル化合物の分割方法 |
US7816533B2 (en) * | 2003-12-15 | 2010-10-19 | Kamaluddin Abdur-Rashid | Asymmetric imine hydrogenation processes |
-
2013
- 2013-01-31 EP EP13153396.0A patent/EP2623509A1/en not_active Withdrawn
- 2013-01-31 JP JP2013017845A patent/JP6173702B2/ja active Active
- 2013-02-01 US US13/757,395 patent/US20130197234A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
JP2013177374A (ja) | 2013-09-09 |
US20130197234A1 (en) | 2013-08-01 |
EP2623509A1 (en) | 2013-08-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Brown et al. | Use of (Cyclopentadienone) iron Tricarbonyl Complexes for C–N Bond Formation Reactions between Amines and Alcohols | |
Mikhailine et al. | Effect of the Structure of the Diamine Backbone of P− N− N− P ligands in Iron (II) Complexes on Catalytic Activity in the Transfer Hydrogenation of Acetophenone | |
EP2294075B1 (en) | Novel ruthenium complexes having hybrid amine ligands, their preparation and use | |
JP5685071B2 (ja) | 新規ルテニウム錯体及びこれを触媒とする光学活性アルコール化合物の製造方法 | |
Chai et al. | Substituent effect on the catalytic activity of ruthenium (II) complexes bearing a pyridyl-supported pyrazolyl-imidazolyl ligand for transfer hydrogenation of ketones | |
US6486337B2 (en) | Ruthenium-disphosphine complexes and their use as catalysts | |
CA2471389A1 (en) | Process for the preparation of nonracemic syn-1-(4-hydroxy-phenyl)-2-(4-hydroxy-4-phenyl-piperidin-1yl)-1-propanol compounds | |
JP6173702B2 (ja) | 光学活性アミン化合物の製造方法 | |
JP5462899B2 (ja) | シン立体配置を有するβ−アミノアルコール類の製造方法 | |
JP2005516036A6 (ja) | 非ラセミsyn−1−(4−ヒドロキシ−フェニル)−2−(4−ヒドロキシ−4−フェニル−ピペリジン−1−イル)−1−プロパノ−ル化合物の製造方法 | |
US8207379B2 (en) | Ruthenium compound and method for producing optically active aminoalcohol compound | |
JPWO2012137460A1 (ja) | 新規ルテニウム錯体及びこれを触媒とする光学活性アルコール化合物の製造方法 | |
US9328079B2 (en) | Process for producing optically active amine | |
JP2005525426A (ja) | ルテニウム錯体を触媒として用いた不活性イミンの水素添加法 | |
EP2865446A1 (en) | Process for producing optically active secondary alcohol | |
EP3016961B1 (en) | Novel ruthenium catalysts and their use for asymmetric reduction of ketones | |
JP5507931B2 (ja) | 芳香族複素環をもつ光学活性アルコールの製造方法 | |
JP2004238306A (ja) | ルテニウムヒドリド錯体、アルコール化合物の製造方法およびラセミ体カルボニル化合物の分割方法 | |
CN114539319B (zh) | 一种手性膦-双环亚磷酰胺酯配体及其制备方法与应用 | |
JP5559767B2 (ja) | ルテニウムヒドリド錯体 | |
JP5685046B2 (ja) | 光学純度低下防止方法 | |
JP4658293B2 (ja) | アンチ立体配置を有する光学活性β−アミノアルコール類の製造方法 | |
JP5330706B2 (ja) | 光学活性3−キヌクリジノールの製造方法 | |
JP2022066019A (ja) | 光学活性なβ-アミノアルコール類の製造方法 | |
JP2022066024A (ja) | 光学活性なヒドロキシエステル類またはヒドロキシアミド類の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20160115 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20160628 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20160705 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20160830 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20161102 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20161215 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20170315 |
|
A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20170512 |
|
RD13 | Notification of appointment of power of sub attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7433 Effective date: 20170523 |
|
TRDD | Decision of grant or rejection written | ||
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20170523 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20170620 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20170705 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6173702 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |