JP2015187092A - 配位子、該配位子を含むニッケル錯体、及び該ニッケル錯体を用いた反応 - Google Patents
配位子、該配位子を含むニッケル錯体、及び該ニッケル錯体を用いた反応 Download PDFInfo
- Publication number
- JP2015187092A JP2015187092A JP2014142721A JP2014142721A JP2015187092A JP 2015187092 A JP2015187092 A JP 2015187092A JP 2014142721 A JP2014142721 A JP 2014142721A JP 2014142721 A JP2014142721 A JP 2014142721A JP 2015187092 A JP2015187092 A JP 2015187092A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- group
- general formula
- nickel
- mhz
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229910052759 nickel Inorganic materials 0.000 title claims abstract description 100
- 239000003446 ligand Substances 0.000 title claims abstract description 68
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 title abstract description 179
- 238000006243 chemical reaction Methods 0.000 title description 31
- 150000001875 compounds Chemical class 0.000 claims abstract description 195
- 150000001728 carbonyl compounds Chemical class 0.000 claims abstract description 84
- 150000002989 phenols Chemical class 0.000 claims abstract description 61
- 150000002815 nickel Chemical group 0.000 claims abstract description 40
- 238000005859 coupling reaction Methods 0.000 claims abstract description 27
- 150000003839 salts Chemical class 0.000 claims abstract description 26
- 238000000034 method Methods 0.000 claims abstract description 25
- 150000002816 nickel compounds Chemical class 0.000 claims abstract description 19
- VURFVHCLMJOLKN-UHFFFAOYSA-N diphosphane Chemical group PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 claims abstract description 14
- -1 arylcarbonyl compound Chemical class 0.000 claims description 45
- 239000003054 catalyst Substances 0.000 claims description 37
- 125000000623 heterocyclic group Chemical group 0.000 claims description 25
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 22
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 16
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 11
- 238000010168 coupling process Methods 0.000 claims description 7
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims 2
- 150000003564 thiocarbonyl compounds Chemical class 0.000 abstract description 52
- 238000006254 arylation reaction Methods 0.000 abstract description 47
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- 238000005481 NMR spectroscopy Methods 0.000 description 122
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 108
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 90
- 125000001424 substituent group Chemical group 0.000 description 64
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 48
- 125000000217 alkyl group Chemical group 0.000 description 29
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical group C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 24
- 125000004437 phosphorous atom Chemical group 0.000 description 23
- 230000015572 biosynthetic process Effects 0.000 description 22
- 238000003786 synthesis reaction Methods 0.000 description 22
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 20
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 19
- 125000005843 halogen group Chemical group 0.000 description 19
- 238000003756 stirring Methods 0.000 description 19
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
- 239000002585 base Substances 0.000 description 18
- 239000000243 solution Substances 0.000 description 18
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 16
- 229910052801 chlorine Inorganic materials 0.000 description 16
- 125000001309 chloro group Chemical group Cl* 0.000 description 16
- 239000007787 solid Substances 0.000 description 16
- 125000001153 fluoro group Chemical group F* 0.000 description 15
- 239000011734 sodium Substances 0.000 description 15
- 239000002904 solvent Substances 0.000 description 15
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 14
- 125000003545 alkoxy group Chemical group 0.000 description 14
- 125000003118 aryl group Chemical group 0.000 description 14
- 229910002091 carbon monoxide Inorganic materials 0.000 description 14
- 229910052731 fluorine Inorganic materials 0.000 description 14
- 239000011521 glass Substances 0.000 description 14
- 239000000203 mixture Substances 0.000 description 14
- 239000002994 raw material Substances 0.000 description 14
- 125000003277 amino group Chemical group 0.000 description 13
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 12
- UORVGPXVDQYIDP-BJUDXGSMSA-N borane Chemical class [10BH3] UORVGPXVDQYIDP-BJUDXGSMSA-N 0.000 description 12
- 239000000460 chlorine Substances 0.000 description 12
- 239000011541 reaction mixture Substances 0.000 description 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
- 125000001072 heteroaryl group Chemical group 0.000 description 11
- 229910052698 phosphorus Inorganic materials 0.000 description 11
- 239000000758 substrate Substances 0.000 description 11
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 10
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 10
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 10
- 150000004945 aromatic hydrocarbons Chemical group 0.000 description 10
- BOUYBUIVMHNXQB-UHFFFAOYSA-N dicyclohexyl(2-dicyclohexylphosphanylethyl)phosphane Chemical compound C1CCCCC1P(C1CCCCC1)CCP(C1CCCCC1)C1CCCCC1 BOUYBUIVMHNXQB-UHFFFAOYSA-N 0.000 description 10
- 125000001188 haloalkyl group Chemical group 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 239000012043 crude product Substances 0.000 description 9
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 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 8
- 238000003818 flash chromatography Methods 0.000 description 8
- 229910052717 sulfur Inorganic materials 0.000 description 8
- 125000004434 sulfur atom Chemical group 0.000 description 8
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 7
- 150000001721 carbon Chemical group 0.000 description 7
- 150000004696 coordination complex Chemical class 0.000 description 7
- 238000000746 purification Methods 0.000 description 7
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000012300 argon atmosphere Substances 0.000 description 6
- MCQRPQCQMGVWIQ-UHFFFAOYSA-N boron;methylsulfanylmethane Chemical compound [B].CSC MCQRPQCQMGVWIQ-UHFFFAOYSA-N 0.000 description 6
- AKJFBIZAEPTXIL-UHFFFAOYSA-N chloro(dicyclohexyl)phosphane Chemical compound C1CCCCC1P(Cl)C1CCCCC1 AKJFBIZAEPTXIL-UHFFFAOYSA-N 0.000 description 6
- LOXJRCIDKVLPQL-UHFFFAOYSA-N dicyclohexyl-(4-dicyclohexylphosphanylthiophen-3-yl)phosphane Chemical compound C1CCCCC1P(C=1C(=CSC=1)P(C1CCCCC1)C1CCCCC1)C1CCCCC1 LOXJRCIDKVLPQL-UHFFFAOYSA-N 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 230000003595 spectral effect Effects 0.000 description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 6
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 5
- 229910052786 argon Inorganic materials 0.000 description 5
- 150000001502 aryl halides Chemical class 0.000 description 5
- 125000001624 naphthyl group Chemical group 0.000 description 5
- 239000011574 phosphorus Substances 0.000 description 5
- 238000001226 reprecipitation Methods 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 125000003107 substituted aryl group Chemical group 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 4
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 4
- VGKLVWTVCUDISO-UHFFFAOYSA-N 3,4-dibromothiophene Chemical compound BrC1=CSC=C1Br VGKLVWTVCUDISO-UHFFFAOYSA-N 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
- 239000007818 Grignard reagent Substances 0.000 description 4
- 125000005129 aryl carbonyl group Chemical group 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- SLFKPACCQUVAPG-UHFFFAOYSA-N carbon monoxide;nickel;triphenylphosphane Chemical compound O=C=[Ni]=C=O.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 SLFKPACCQUVAPG-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 150000004292 cyclic ethers Chemical class 0.000 description 4
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 4
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 229910052740 iodine Inorganic materials 0.000 description 4
- 238000002955 isolation Methods 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229910052744 lithium Inorganic materials 0.000 description 4
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 125000004430 oxygen atom Chemical group O* 0.000 description 4
- 229910000160 potassium phosphate Inorganic materials 0.000 description 4
- 235000011009 potassium phosphates Nutrition 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- 229960000549 4-dimethylaminophenol Drugs 0.000 description 3
- QJNLUNBGDFUULX-UHFFFAOYSA-N 4-n,4-n'-dimethyl-3h-pyridine-4,4-diamine Chemical compound CNC1(NC)CC=NC=C1 QJNLUNBGDFUULX-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 0 CP(*)(*(C1)CCCCCC1(*)P1(*)*)*1(*)I Chemical compound CP(*)(*(C1)CCCCCC1(*)P1(*)*)*1(*)I 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 3
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 125000004104 aryloxy group Chemical group 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 3
- 229910000024 caesium carbonate Inorganic materials 0.000 description 3
- 239000007819 coupling partner Substances 0.000 description 3
- DZNBZPKZOBDXEL-UHFFFAOYSA-N dicyclohexyl-(2-dicyclohexylphosphanylphenyl)phosphane Chemical compound C1CCCCC1P(C=1C(=CC=CC=1)P(C1CCCCC1)C1CCCCC1)C1CCCCC1 DZNBZPKZOBDXEL-UHFFFAOYSA-N 0.000 description 3
- 229910001873 dinitrogen Inorganic materials 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 150000004795 grignard reagents Chemical class 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 125000001041 indolyl group Chemical group 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 3
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 3
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 3
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 238000012746 preparative thin layer chromatography Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- WUTPXBXSEMJIDW-HNNXBMFYSA-N (2s)-2-(benzylamino)-3-(4-hydroxyphenyl)propanoic acid Chemical compound C([C@@H](C(=O)O)NCC=1C=CC=CC=1)C1=CC=C(O)C=C1 WUTPXBXSEMJIDW-HNNXBMFYSA-N 0.000 description 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 2
- OTKCEEWUXHVZQI-UHFFFAOYSA-N 1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(=O)CC1=CC=CC=C1 OTKCEEWUXHVZQI-UHFFFAOYSA-N 0.000 description 2
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 2
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 2
- YQTCQNIPQMJNTI-UHFFFAOYSA-N 2,2-dimethylpropan-1-one Chemical group CC(C)(C)[C]=O YQTCQNIPQMJNTI-UHFFFAOYSA-N 0.000 description 2
- JVSFQJZRHXAUGT-UHFFFAOYSA-N 2,2-dimethylpropanoyl chloride Chemical compound CC(C)(C)C(Cl)=O JVSFQJZRHXAUGT-UHFFFAOYSA-N 0.000 description 2
- FGXXGOHICBSKBW-UHFFFAOYSA-N 2-[bis(furan-2-yl)methyl]furan Chemical compound C1=COC(C(C=2OC=CC=2)C=2OC=CC=2)=C1 FGXXGOHICBSKBW-UHFFFAOYSA-N 0.000 description 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 2
- CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 2
- 150000008041 alkali metal carbonates Chemical class 0.000 description 2
- 229910000318 alkali metal phosphate Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- SBWAJHLQMFBNIN-UHFFFAOYSA-N dichloro(2-dichlorophosphanylethyl)phosphane Chemical compound ClP(Cl)CCP(Cl)Cl SBWAJHLQMFBNIN-UHFFFAOYSA-N 0.000 description 2
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- BLHLJVCOVBYQQS-UHFFFAOYSA-N ethyllithium Chemical compound [Li]CC BLHLJVCOVBYQQS-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 229910000103 lithium hydride Inorganic materials 0.000 description 2
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 2
- HYRDTOIPWXXZCJ-UHFFFAOYSA-N n-benzyl-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NCC1=CC=CC=C1 HYRDTOIPWXXZCJ-UHFFFAOYSA-N 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 125000002971 oxazolyl group Chemical group 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 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 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- NHKJPPKXDNZFBJ-UHFFFAOYSA-N phenyllithium Chemical compound [Li]C1=CC=CC=C1 NHKJPPKXDNZFBJ-UHFFFAOYSA-N 0.000 description 2
- 125000003373 pyrazinyl group Chemical group 0.000 description 2
- 125000003226 pyrazolyl group Chemical group 0.000 description 2
- 125000000168 pyrrolyl group Chemical group 0.000 description 2
- WPFGFHJALYCVMO-UHFFFAOYSA-L rubidium carbonate Chemical compound [Rb+].[Rb+].[O-]C([O-])=O WPFGFHJALYCVMO-UHFFFAOYSA-L 0.000 description 2
- 229910000026 rubidium carbonate Inorganic materials 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000012312 sodium hydride Substances 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 description 2
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 125000005415 substituted alkoxy group Chemical group 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- JRTIUDXYIUKIIE-KZUMESAESA-N (1z,5z)-cycloocta-1,5-diene;nickel Chemical compound [Ni].C\1C\C=C/CC\C=C/1.C\1C\C=C/CC\C=C/1 JRTIUDXYIUKIIE-KZUMESAESA-N 0.000 description 1
- LWNGJAHMBMVCJR-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenoxy)boronic acid Chemical compound OB(O)OC1=C(F)C(F)=C(F)C(F)=C1F LWNGJAHMBMVCJR-UHFFFAOYSA-N 0.000 description 1
- QFPIIICNJHDAKC-UHFFFAOYSA-N (2-bromophenyl)-dicyclohexylphosphane Chemical compound BrC1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 QFPIIICNJHDAKC-UHFFFAOYSA-N 0.000 description 1
- VPMIAOSOTOODMY-KJAPKAAFSA-N (4r)-6-[(e)-2-[6-tert-butyl-4-(4-fluorophenyl)-2-propan-2-ylpyridin-3-yl]ethenyl]-4-hydroxyoxan-2-one Chemical compound C([C@H](O)C1)C(=O)OC1/C=C/C=1C(C(C)C)=NC(C(C)(C)C)=CC=1C1=CC=C(F)C=C1 VPMIAOSOTOODMY-KJAPKAAFSA-N 0.000 description 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 description 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 1
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
- UKQCJCWLKWRFFI-UHFFFAOYSA-N 1,2,2-triphenylethanone Chemical compound C=1C=CC=CC=1C(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 UKQCJCWLKWRFFI-UHFFFAOYSA-N 0.000 description 1
- WQONPSCCEXUXTQ-UHFFFAOYSA-N 1,2-dibromobenzene Chemical compound BrC1=CC=CC=C1Br WQONPSCCEXUXTQ-UHFFFAOYSA-N 0.000 description 1
- JYXLALOINIPOMH-UHFFFAOYSA-N 1,2-diphenyl-2-(4-phenylphenyl)ethanone Chemical compound C=1C=CC=CC=1C(=O)C(C=1C=CC(=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 JYXLALOINIPOMH-UHFFFAOYSA-N 0.000 description 1
- IVWOXPKJQVHVBG-UHFFFAOYSA-N 1-(4-fluorophenyl)-2-naphthalen-1-ylethanone Chemical compound C1=CC(F)=CC=C1C(=O)CC1=CC=CC2=CC=CC=C12 IVWOXPKJQVHVBG-UHFFFAOYSA-N 0.000 description 1
- WJWBKYJUXGQMRZ-UHFFFAOYSA-N 1-(4-methoxyphenyl)-2-naphthalen-1-ylethanone Chemical compound C1=CC(OC)=CC=C1C(=O)CC1=CC=CC2=CC=CC=C12 WJWBKYJUXGQMRZ-UHFFFAOYSA-N 0.000 description 1
- MZGOBFVIXXEWCW-UHFFFAOYSA-N 1-(4-methylphenyl)-2-naphthalen-1-ylethanone Chemical compound C1=CC(C)=CC=C1C(=O)CC1=CC=CC2=CC=CC=C12 MZGOBFVIXXEWCW-UHFFFAOYSA-N 0.000 description 1
- VEZWDKMQJVMFHD-UHFFFAOYSA-N 1-(furan-2-yl)-2-naphthalen-1-ylethanone Chemical compound C=1C=CC2=CC=CC=C2C=1CC(=O)C1=CC=CO1 VEZWDKMQJVMFHD-UHFFFAOYSA-N 0.000 description 1
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical group C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical group C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 1
- RFCWFIMOCBDYBD-UHFFFAOYSA-N 1-methyl-3-(4-phenylphenyl)-3h-indol-2-one Chemical compound C12=CC=CC=C2N(C)C(=O)C1C(C=C1)=CC=C1C1=CC=CC=C1 RFCWFIMOCBDYBD-UHFFFAOYSA-N 0.000 description 1
- ZVXPPUHLTRYVBP-UHFFFAOYSA-N 1-methyl-3-naphthalen-2-ylpyrrolidine-2,5-dione Chemical compound O=C1N(C)C(=O)CC1C1=CC=C(C=CC=C2)C2=C1 ZVXPPUHLTRYVBP-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- OSTWOIBSEBPRSM-UHFFFAOYSA-N 2-(4-methoxyphenyl)-1,2-diphenylethanone Chemical compound C1=CC(OC)=CC=C1C(C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 OSTWOIBSEBPRSM-UHFFFAOYSA-N 0.000 description 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- KSGPLUCEZUTFRS-UHFFFAOYSA-N 2-naphthalen-1-yl-1-pyridin-3-ylethanone Chemical compound C=1C=CC2=CC=CC=C2C=1CC(=O)C1=CC=CN=C1 KSGPLUCEZUTFRS-UHFFFAOYSA-N 0.000 description 1
- FXVUYCWKGCIRNQ-UHFFFAOYSA-N 2-naphthalen-1-yl-1-thiophen-2-ylethanone Chemical compound C=1C=CC2=CC=CC=C2C=1CC(=O)C1=CC=CS1 FXVUYCWKGCIRNQ-UHFFFAOYSA-N 0.000 description 1
- ICMPBQHLJHBNEX-UHFFFAOYSA-N 2-naphthalen-2-yl-1-phenylpropan-1-one Chemical compound C=1C=C2C=CC=CC2=CC=1C(C)C(=O)C1=CC=CC=C1 ICMPBQHLJHBNEX-UHFFFAOYSA-N 0.000 description 1
- RIZNUXVSKZMCDI-UHFFFAOYSA-N 3,3-dimethyl-1-naphthalen-1-ylbutan-2-one Chemical compound C1=CC=C2C(CC(=O)C(C)(C)C)=CC=CC2=C1 RIZNUXVSKZMCDI-UHFFFAOYSA-N 0.000 description 1
- SSFVEOQDTNIHOV-UHFFFAOYSA-N 3,3-dimethyl-1-naphthalen-2-ylbutan-2-one Chemical compound C1=CC=CC2=CC(CC(=O)C(C)(C)C)=CC=C21 SSFVEOQDTNIHOV-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- HLBOAQSKBNNHMW-UHFFFAOYSA-N 3-(3-methoxyphenyl)pyridine Chemical compound COC1=CC=CC(C=2C=NC=CC=2)=C1 HLBOAQSKBNNHMW-UHFFFAOYSA-N 0.000 description 1
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 description 1
- LTPOSIZJPSDSIL-UHFFFAOYSA-N 5,6-diphenylmorpholin-2-one Chemical compound O1C(=O)CNC(C=2C=CC=CC=2)C1C1=CC=CC=C1 LTPOSIZJPSDSIL-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- MPFSQYKXIQEDED-UHFFFAOYSA-N B.BrC1=CSC=C1P(C1CCCCC1)C1CCCCC1 Chemical compound B.BrC1=CSC=C1P(C1CCCCC1)C1CCCCC1 MPFSQYKXIQEDED-UHFFFAOYSA-N 0.000 description 1
- AGSNXOCSAUASFN-UHFFFAOYSA-N B.Brc1ccccc1P(C1CCCCC1)C1CCCCC1 Chemical compound B.Brc1ccccc1P(C1CCCCC1)C1CCCCC1 AGSNXOCSAUASFN-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- MYEDOEALOOWEHN-UHFFFAOYSA-N C(=O)=[Ni]=C=O.C1(CCC1)P(CCP(C1CCC1)C1CCC1)C1CCC1 Chemical compound C(=O)=[Ni]=C=O.C1(CCC1)P(CCP(C1CCC1)C1CCC1)C1CCC1 MYEDOEALOOWEHN-UHFFFAOYSA-N 0.000 description 1
- RZGINKWSNXMUJP-UHFFFAOYSA-N C(=O)=[Ni]=C=O.C1(CCCC1)P(CCP(C1CCCC1)C1CCCC1)C1CCCC1 Chemical compound C(=O)=[Ni]=C=O.C1(CCCC1)P(CCP(C1CCCC1)C1CCCC1)C1CCCC1 RZGINKWSNXMUJP-UHFFFAOYSA-N 0.000 description 1
- KMCGEDBVKZXJLA-UHFFFAOYSA-N C(=O)=[Ni]=C=O.C1(CCCCC1)P(C1=C(C=CC=C1)P(C1CCCCC1)C1CCCCC1)C1CCCCC1 Chemical compound C(=O)=[Ni]=C=O.C1(CCCCC1)P(C1=C(C=CC=C1)P(C1CCCCC1)C1CCCCC1)C1CCCCC1 KMCGEDBVKZXJLA-UHFFFAOYSA-N 0.000 description 1
- FYZNHXXIUSKJGI-UHFFFAOYSA-N C(=O)=[Ni]=C=O.C1(CCCCC1)P(C1=CSC=C1P(C1CCCCC1)C1CCCCC1)C1CCCCC1 Chemical compound C(=O)=[Ni]=C=O.C1(CCCCC1)P(C1=CSC=C1P(C1CCCCC1)C1CCCCC1)C1CCCCC1 FYZNHXXIUSKJGI-UHFFFAOYSA-N 0.000 description 1
- ISGBKKVCFYNFEI-UHFFFAOYSA-N C(=O)=[Ni]=C=O.C1(CCCCCC1)P(CCP(C1CCCCCC1)C1CCCCCC1)C1CCCCCC1 Chemical compound C(=O)=[Ni]=C=O.C1(CCCCCC1)P(CCP(C1CCCCCC1)C1CCCCCC1)C1CCCCCC1 ISGBKKVCFYNFEI-UHFFFAOYSA-N 0.000 description 1
- CZAJFYPGRAOVCO-UHFFFAOYSA-N C1(=CC=CC2=CC=CC=C12)CC(=O)C1=CC(=C(C(=C1)OC)OC)OC Chemical compound C1(=CC=CC2=CC=CC=C12)CC(=O)C1=CC(=C(C(=C1)OC)OC)OC CZAJFYPGRAOVCO-UHFFFAOYSA-N 0.000 description 1
- IRWWOFPQARRPTA-UHFFFAOYSA-N C1(=CC=CC2=CC=CC=C12)CC(=O)C1=CC=C(C=C1)C(F)(F)F Chemical compound C1(=CC=CC2=CC=CC=C12)CC(=O)C1=CC=C(C=C1)C(F)(F)F IRWWOFPQARRPTA-UHFFFAOYSA-N 0.000 description 1
- JDBXLSSULHWUJX-UHFFFAOYSA-N C1(=CC=CC=C1)C(C(C=1C=C2C=CC=NC2=CC=1)C1=CC=CC=C1)=O Chemical compound C1(=CC=CC=C1)C(C(C=1C=C2C=CC=NC2=CC=1)C1=CC=CC=C1)=O JDBXLSSULHWUJX-UHFFFAOYSA-N 0.000 description 1
- PBDVCFHBWKPQIO-UHFFFAOYSA-N C1=C(C=CC2=CC=CC=C12)C1C(N(C2=CC=CC=C12)C1=CC=CC=C1)=O Chemical compound C1=C(C=CC2=CC=CC=C12)C1C(N(C2=CC=CC=C12)C1=CC=CC=C1)=O PBDVCFHBWKPQIO-UHFFFAOYSA-N 0.000 description 1
- QZBGMQLALIXOIA-UHFFFAOYSA-N CC(C(C(=O)C1=CC=CC=C1)C1=CC2=CC=CC=C2C=C1)C Chemical compound CC(C(C(=O)C1=CC=CC=C1)C1=CC2=CC=CC=C2C=C1)C QZBGMQLALIXOIA-UHFFFAOYSA-N 0.000 description 1
- RJNPPEUAJCEUPV-UHFFFAOYSA-N CC(Oc1cc2ccccc2cc1)=O Chemical compound CC(Oc1cc2ccccc2cc1)=O RJNPPEUAJCEUPV-UHFFFAOYSA-N 0.000 description 1
- CZZRVWNWRSTLJS-UHFFFAOYSA-N CC=1C=C(C=C(C=1)C)C1C(N(C2=CC=CC=C12)C)=O Chemical compound CC=1C=C(C=C(C=1)C)C1C(N(C2=CC=CC=C12)C)=O CZZRVWNWRSTLJS-UHFFFAOYSA-N 0.000 description 1
- ASXWWEZTWWRIOY-UHFFFAOYSA-N CN(C1=CC=C(C=C1)C(CC1=CC=CC2=CC=CC=C12)=O)C Chemical compound CN(C1=CC=C(C=C1)C(CC1=CC=CC2=CC=CC=C12)=O)C ASXWWEZTWWRIOY-UHFFFAOYSA-N 0.000 description 1
- NGJNDDDECRNDBG-UHFFFAOYSA-N CN1C(C(C2=CC=CC=C12)C1=CC2=CC=CC=C2C=C1)=O Chemical compound CN1C(C(C2=CC=CC=C12)C1=CC2=CC=CC=C2C=C1)=O NGJNDDDECRNDBG-UHFFFAOYSA-N 0.000 description 1
- AVNLNELZONLXMJ-UHFFFAOYSA-N CN1C(C(C2=CC=CC=C12)C=1C=C2C=CC(=CC2=CC=1)C(=O)OC)=O Chemical compound CN1C(C(C2=CC=CC=C12)C=1C=C2C=CC(=CC2=CC=1)C(=O)OC)=O AVNLNELZONLXMJ-UHFFFAOYSA-N 0.000 description 1
- DUHZFPMXQBSXLD-UHFFFAOYSA-N CN1C(C(CC1)C1=CC2=CC=CC=C2C=C1)=S Chemical compound CN1C(C(CC1)C1=CC2=CC=CC=C2C=C1)=S DUHZFPMXQBSXLD-UHFFFAOYSA-N 0.000 description 1
- DJRHIBBPWJWKGK-UHFFFAOYSA-N CN1C=C(C2=CC=CC=C12)C(CC1=CC=CC2=CC=CC=C12)=O Chemical compound CN1C=C(C2=CC=CC=C12)C(CC1=CC=CC2=CC=CC=C12)=O DJRHIBBPWJWKGK-UHFFFAOYSA-N 0.000 description 1
- OGNHOYDPXOEUDG-UHFFFAOYSA-N CN1C=C(C=C1)C(CC1=CC=CC2=CC=CC=C12)=O Chemical compound CN1C=C(C=C1)C(CC1=CC=CC2=CC=CC=C12)=O OGNHOYDPXOEUDG-UHFFFAOYSA-N 0.000 description 1
- DOQDFTOFUXHVGY-UHFFFAOYSA-N COC(=O)C1=CC2=C(C=C1)C=C(OC(=O)N(C)C)C=C2 Chemical compound COC(=O)C1=CC2=C(C=C1)C=C(OC(=O)N(C)C)C=C2 DOQDFTOFUXHVGY-UHFFFAOYSA-N 0.000 description 1
- WRGORBKBGGABHM-UHFFFAOYSA-N COC(C(C1=CC=C(C=C1)OC)C=1C=C2C=CC(=CC2=CC=1)C(=O)OC)=O Chemical compound COC(C(C1=CC=C(C=C1)OC)C=1C=C2C=CC(=CC2=CC=1)C(=O)OC)=O WRGORBKBGGABHM-UHFFFAOYSA-N 0.000 description 1
- XCDJOYBMMASVIQ-UHFFFAOYSA-N COC1=CC=C(C2=CC=CC=C12)CC(=O)C1=CC=C(C=C1)OC Chemical compound COC1=CC=C(C2=CC=CC=C12)CC(=O)C1=CC=C(C=C1)OC XCDJOYBMMASVIQ-UHFFFAOYSA-N 0.000 description 1
- UYIFQDHOKGOPHS-UHFFFAOYSA-N COC1=CC=C(C=C1)C(C(=O)OC)C=1C=C2C=CC=NC2=CC=1 Chemical compound COC1=CC=C(C=C1)C(C(=O)OC)C=1C=C2C=CC=NC2=CC=1 UYIFQDHOKGOPHS-UHFFFAOYSA-N 0.000 description 1
- CFTXCSHYDSSNAN-UHFFFAOYSA-N COC1=CC=C(C=C1)C(CC1=C2C=CC=NC2=CC=C1)=O Chemical compound COC1=CC=C(C=C1)C(CC1=C2C=CC=NC2=CC=C1)=O CFTXCSHYDSSNAN-UHFFFAOYSA-N 0.000 description 1
- KQUDJIDBJYNUKW-UHFFFAOYSA-N COC1=CC=C(C=C1)C(CC=1C=C2C=CC(=CC2=CC=1)C(=O)OC)=O Chemical compound COC1=CC=C(C=C1)C(CC=1C=C2C=CC(=CC2=CC=1)C(=O)OC)=O KQUDJIDBJYNUKW-UHFFFAOYSA-N 0.000 description 1
- ZXRWIWFSMNAGMF-UHFFFAOYSA-N COC1=CC=C(C=C1)C(CC=1C=CC=C2C=CC=NC=12)=O Chemical compound COC1=CC=C(C=C1)C(CC=1C=CC=C2C=CC=NC=12)=O ZXRWIWFSMNAGMF-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 208000033962 Fontaine progeroid syndrome Diseases 0.000 description 1
- 241000276457 Gadidae Species 0.000 description 1
- 238000003747 Grignard reaction Methods 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- WMSCYOVZQADJGD-UHFFFAOYSA-N O=C(C(C1=CC=CC=C1)C=1C=C2C=CC(=CC2=CC=1)C(=O)OC)C1=CC=CC=C1 Chemical compound O=C(C(C1=CC=CC=C1)C=1C=C2C=CC(=CC2=CC=1)C(=O)OC)C1=CC=CC=C1 WMSCYOVZQADJGD-UHFFFAOYSA-N 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- RISXKBIOEWVNKL-UHFFFAOYSA-N [2,3-bis(trifluoromethyl)phenoxy]boronic acid Chemical compound OB(O)OC1=CC=CC(C(F)(F)F)=C1C(F)(F)F RISXKBIOEWVNKL-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229910000102 alkali metal hydride Inorganic materials 0.000 description 1
- 150000008046 alkali metal hydrides Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000005577 anthracene group Chemical group 0.000 description 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
- 125000005110 aryl thio group Chemical group 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 229910000085 borane Inorganic materials 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- UTZVRFPLSSHYGF-UHFFFAOYSA-N carboxy(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)C(O)=O UTZVRFPLSSHYGF-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 150000003950 cyclic amides Chemical class 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- PWYCJOQUUOWWSM-UHFFFAOYSA-N dioxane;toluene Chemical compound C1CCOOC1.CC1=CC=CC=C1 PWYCJOQUUOWWSM-UHFFFAOYSA-N 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- NPGRKOXTMDEQJS-UHFFFAOYSA-N ethyl 2-naphthalen-2-yl-2-phenylacetate Chemical compound C1=C(C=CC2=CC=CC=C12)C(C(=O)OCC)C1=CC=CC=C1 NPGRKOXTMDEQJS-UHFFFAOYSA-N 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 1
- YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 1
- 229910001386 lithium phosphate Inorganic materials 0.000 description 1
- LZWQNOHZMQIFBX-UHFFFAOYSA-N lithium;2-methylpropan-2-olate Chemical compound [Li+].CC(C)(C)[O-] LZWQNOHZMQIFBX-UHFFFAOYSA-N 0.000 description 1
- 229910001623 magnesium bromide Inorganic materials 0.000 description 1
- GFTXWCQFWLOXAT-UHFFFAOYSA-M magnesium;cyclohexane;bromide Chemical compound [Mg+2].[Br-].C1CC[CH-]CC1 GFTXWCQFWLOXAT-UHFFFAOYSA-M 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000010814 metallic waste Substances 0.000 description 1
- MWZPENIJLUWBSY-VIFPVBQESA-N methyl L-tyrosinate Chemical compound COC(=O)[C@@H](N)CC1=CC=C(O)C=C1 MWZPENIJLUWBSY-VIFPVBQESA-N 0.000 description 1
- XLSZMDLNRCVEIJ-UHFFFAOYSA-N methylimidazole Natural products CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000006606 n-butoxy group Chemical group 0.000 description 1
- 125000005186 naphthyloxy group Chemical group C1(=CC=CC2=CC=CC=C12)O* 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000004533 oil dispersion Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000004043 oxo group Chemical group O=* 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- IUBQJLUDMLPAGT-UHFFFAOYSA-N potassium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([K])[Si](C)(C)C IUBQJLUDMLPAGT-UHFFFAOYSA-N 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 125000005920 sec-butoxy group Chemical group 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- WRIKHQLVHPKCJU-UHFFFAOYSA-N sodium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([Na])[Si](C)(C)C WRIKHQLVHPKCJU-UHFFFAOYSA-N 0.000 description 1
- BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- TWQULNDIKKJZPH-UHFFFAOYSA-K trilithium;phosphate Chemical compound [Li+].[Li+].[Li+].[O-]P([O-])([O-])=O TWQULNDIKKJZPH-UHFFFAOYSA-K 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 238000012982 x-ray structure analysis Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B37/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving either the formation of a carbon-to-carbon bond between two carbon atoms not directly linked already or the disconnection of two directly linked carbon atoms
- C07B37/04—Substitution
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
- B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
- B01J31/2409—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring with more than one complexing phosphine-P atom
- B01J31/2414—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring with more than one complexing phosphine-P atom comprising aliphatic or saturated rings
-
- 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
- C07F15/04—Nickel compounds
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms
- C07F9/655345—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
- B01J2231/42—Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
- B01J2231/4205—C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type
- B01J2231/4272—C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type via enolates or aza-analogues, added as such or made in-situ, e.g. ArY + R2C=C(OM)Z -> ArR2C-C(O)Z, in which R is H or alkyl, M is Na, K or SiMe3, Y is the leaving group, Z is Ar or OR' and R' is alkyl
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/847—Nickel
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2540/00—Compositional aspects of coordination complexes or ligands in catalyst systems
- B01J2540/30—Non-coordinating groups comprising sulfur
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Indole Compounds (AREA)
- Catalysts (AREA)
Abstract
【解決手段】本発明の新規化合物は、5員環又は6員環のヘテロ環に、ジアルキルホスフィン及び/又はジシクロアルキルホスフィンが2個置換されたダイホスフィン骨格を有する化合物若しくはその塩、並びに該ダイホスフィン骨格がニッケル原子に結合している化合物である。また、単座又は二座のジアルキルホスフィン及び/又はジシクロアルキルホスフィン骨格を有するニッケル化合物の存在下で、カルボニル化合物とフェノール誘導体とのカップリング反応を進行させることができる。
【選択図】なし
Description
で示される、項1に記載の化合物又はその塩。
で示される、項5に記載の化合物。
前記カップリング反応は、単座又は二座のジアルキルホスフィン及び/又はジシクロアルキルホスフィン骨格を有するニッケル化合物の存在下で行う、製造方法。
で示される化合物である、項11に記載の製造方法。
前記反応は、単座又は二座のジアルキルホスフィン及び/又はジシクロアルキルホスフィン骨格を有するニッケル化合物の存在下で行う、方法。
で示される化合物である、項13に記載の方法。
(1)配位子化合物
本発明の配位子化合物は、5員環又は6員環のヘテロ環に、ジアルキルホスフィン及び/又はジシクロアルキルホスフィンが2個置換されたダイホスフィン骨格を有する化合物、又はその塩であり、文献未記載の新規化合物である。この配位子化合物は、ニッケル原子に2座(2個のリン原子)で配位して錯体を形成することができる。
で示される化合物、又はその塩である。
で示される化合物が好ましく、一般式(1A1):
で示される化合物がより好ましい。
で示される化合物が好ましく、一般式(1B1):
で示される化合物がより好ましい。
本発明のニッケル錯体は、5員環又は6員環のヘテロ環に、ジアルキルホスフィン及び/又はジシクロアルキルホスフィンが2個置換されたダイホスフィン骨格を有し、且つ、該ダイホスフィン骨格が、ニッケル原子に結合(特に配位結合)している、化合物であり、文献未記載の新規化合物である。このニッケル錯体は、より安価なフェノール誘導体を用いた場合であっても、カルボニル化合物又はチオカルボニル化合物のアリール化(特にαアリール化)に用いる触媒として利用できる。また、本発明のニッケル錯体を触媒として使用すると、カルボニル化合物又はチオカルボニル化合物のアリール化(特にαアリール化)を高収率に行わせることができるとともに、保存安定性にも優れるため、カルボニル化合物又はチオカルボニル化合物のアリール化(特にαアリール化)に用いる触媒として特に有用である。
で示される化合物が好ましい。
で示される化合物が好ましく、一般式(2A1):
で示される化合物が好ましい。
で示される化合物が好ましく、一般式(2B1):
で示される化合物がより好ましい。
等が挙げられる。
一般式(1)で示される配位子化合物及び一般式(2)で示されるニッケル錯体は、例えば、次の反応式:
にしたがって製造することができる。
一般式(1)で示される本発明の配位子化合物は、例えば、一般式(4)で表される化合物に、塩基の存在下に、一般式(5):
R1R2P−X5
[式中、R1及びR2は前記に同じ;X5はハロゲン原子である。]
で表されるリン化合物を反応させて、製造することができる。
一般式(1)で示される本発明の配位子化合物又はその塩に、ニッケル(Ni)化合物を反応させて、一般式(2)で表されるニッケル錯体(本発明のニッケル錯体)を製造することができる。
本発明のニッケル錯体(触媒)は、カルボニル化合物又はチオカルボニル化合物とフェノール誘導体とを効果的にカップリング反応させて、アリール(チオ)カルボニル化合物(特にαアリール(チオ)カルボニル化合物)を得るための触媒として有用である。なお、本明細書において、アリール(チオ)カルボニル化合物とは、アリールカルボニル化合物又はアリールチオカルボニル化合物を意味し、αアリール(チオ)カルボニル化合物とは、αアリールカルボニル化合物又はαアリールチオカルボニル化合物を意味する。
で示される化合物を採用できる。
を採用することもできる。
で示される化合物が好ましく、一般式(7A1):
で示される化合物がより好ましい。
等を使用することができる。
で示される化合物を採用できる。
で示される化合物が好ましく、一般式(6A1):
で示される化合物がより好ましい。
で示される化合物が好ましい。
で示される化合物を意味する。
等を使用することができる。
で示される化合物がより好ましく、収率の観点から、一般式(2)で示される本発明のニッケル錯体(触媒)が特に好ましい。最も好ましいのは、上記ニッケル錯体(3B1)である。
後述の実施例においても説明するように、以下の式:
で示されるニッケル錯体(触媒)と、以下の式:
が得られる。
[合成例1−1:フェノール誘導体2a〜2f、2h〜2j及び2n〜2t]
以下の表1に記載の化合物を、以下の表1に記載の文献の方法にしたがって得た。
2a、2c、2e、2h、2i: J. Am. Chem. Soc., 2008, 130, 14422-14423
2b、2j: J. Am. Chem. Soc., 2012, 134, 169-172
2d:T. Bull. Chem. Soc. Jpn., 2004, 77, 569-574
2f:Tetrahedron, 2005, 61, 6652-6656
2n:J. Org. Chem., 2006, 71, 5785-5788
2o:J. Am. Chem. Soc., 2009, 131, 17748-17749
2p:J. Am. Chem. Soc., 2008, 130, 13848-13849
2q:Synth. Commun., 1997, 27, 3035
2r:J. Phys. Org. Chem., 2011, 24, 1081-1087
2s: J. Am. Chem. Soc., 2012, 134, 8298-8301
2t:Tetrahedron, 2002, 58, 2965-2972。
1H NMR (400 MHz, CDCl3) δ 7.60-7.54 (m, 4H), 7.46-7.41 (m, 2H), 7.34 (tt, J = 7.2, 5.2 Hz, 1H), 7.13 (d, J = 8.8 Hz, 1H), 1.38 (s, 9H); 13C NMR (100 MHz, CDCl3) δ 177.1, 150.5, 140.4, 138.7, 128.8, 128.1, 127.3, 127.1, 121.7, 39.1, 27.1; HRMS (ESI) m/z calcd for C17H19O2 + [M+H]+: 255.1380 found 255.1369。
1H NMR (600 MHz, CDCl3) δ 7.28 (d, J = 8.4 Hz, 1H), 7.46-7.41 (m, 2H), 7.34 (tt, J = 7.2, 1.2 Hz, 1H), 7.13 (d, J = 8.8 Hz, 2H), 1.38 (s, 9H); 13C NMR (150 MHz, CDCl3) δ 220.8, 177.3, 149.0, 137.9, 137.1, 126.3, 121.5, 118.6, 50.4, 47.9, 44.1, 39.0, 38.0, 35.9, 31.5, 29.4, 27.1, 26.3, 25.8, 21.6, 13.8; HRMS (ESI) m/z calcd for C23H30NaO3 +[M+Na]+: 377.2087 found 377.2077。
[合成例2−1:ニッケル錯体3bの合成]
グリニャール試薬として、適切な材料を用いること以外は合成例2−1と同様の手法により、以下の表1に示す化合物を得た。
1H NMR (600 MHz, C6D6) δ 2.47-2.35 (m, 4H), 2.29-2.13 (m, 4H), 2.13-1.86 (m, 16H), 1.86-1.72 (m, 4H), 1.04 (d, J = 10.8 Hz, 4H); 13C NMR (150 MHz, C6D6) δ 204.3, 33.5 (t, JPC = 8.6 Hz), 25.7, 24.8, 24.1 (t, JPC = 20.1 Hz), 21.3 (t, JPC = 8.6 Hz); 31P NMR (160 MHz, C6D6) δ60.9; IR (neat): 1984.4, 1912.1 cm-1; HRMS (FAB+): m/z calcd for C19H32NiOP2 [M-CO]+: 396.1282; found 396.1287。
1H NMR (400 MHz, C6D6) δ 2.03-1.60 (m, 20H), 1.60-1.20 (m, 36H). 13C NMR (100 MHz, C6D6) δ 204.3, 37.1 (t, JPC = 7.2 Hz), 30.6 (d, JPC = 8.6 Hz), 29.3-29.0 (m), 28.2 (d, JPC = 21.1 Hz), 24.3 (t, JPC = 18.2 Hz); 31P NMR (160 MHz, C6D6) δ 74.9; IR (neat): 1980.5, 1916.9 cm-1; HRMS (FAB+): m/z calcd for C31H56NiOP2[M-CO]+: 564.3160; found 564.3158。
[実施例1−1]
磁気撹拌子を入れた50 mLの丸底ガラスフラスコに、3,4−ジブロモチオフェン(1.1 mL, 9.92 mmol)、及び乾燥ジエチルエーテル(10 mL)を加えた。-78℃に冷却した後、n−ブチルリチウムのヘキサン溶液(1.6 M, 6.1 mL, 1.0当量)を-78℃で10分間かけて添加した。-78℃で1時間攪拌した後、クロロジシクロヘキシルホスフィン(2.3 mL, 10.4 mmol, 1.05当量)のジエチルエーテル(5.0 mL)溶液を-78℃で15分間かけて添加した。-78℃で30分間攪拌した後、n−ブチルリチウムのヘキサン溶液(1.6 M, 6.1 mL, 1.0当量)を-78℃で10分間かけて添加した。-78℃で1時間攪拌した後、クロロジシクロヘキシルホスフィン(2.3 mL, 10.4 mmol, 1.05当量)のジエチルエーテル(5.0 mL)溶液を-78℃で10分間かけて添加した。その後、反応混合物を-78℃で30分間攪拌した。室温まで温めた後、反応混合物を水でクエンチし、ヘキサンで抽出し、食塩水で洗浄し、Na2SO4で乾燥し、減圧下に濃縮した。粗生成物をトルエン(1.0 mL)による再沈殿により精製し、3,4−ビス(ジシクロヘキシルホスフィノ)チオフェン(dcypt;配位子3f’)を白色固体として得た(3.05 g, 65%)。
[実施例2−1]
[実施例3−1]
原料として、カルボニル化合物(1a)及びフェノール誘導体(2a)の代わりに種々の原料を使用して実施例3−1と同様の手法により(必要に応じて精製方法を適宜変更して)、以下の表2に示す化合物を得た。
1H NMR (400 MHz, CDCl3) δ 8.87 (dd, J = 4.4, 1.6 Hz, 1H), 8.10-8.02 (m, 4H), 7.66 (m, 2H), 7.52 (t, J = 8.0 Hz, 1H), 7.42 (t, J = 8.0 Hz, 2H), 7.38-7.31 (m, 5H), 7.29-7.25 (m, 1H), 6.24 (s, 1H); 13C NMR (100 MHz, CDCl3) δ 197.9, 150.4, 147.4, 138.4, 137.6, 136.5, 136.0, 133.2, 131.0, 129.8, 129.1, 129.0, 128.9, 128.7, 128.1, 127.5, 127.4, 121.3, 59.1; HRMS (ESI) m/z calcd for C23H18NO+[M+H]+: 324.1383 found 324.1373。
1H NMR (400 MHz, CDCl3) δ 8.56 (s, 1H), 8.06-8.00 (m, 3H), 7.92 (d, J = 8.4 Hz, 1H), 7.79 (d, J = 8.4 Hz, 1H), 7.71 (s, 1H), 7.56-7.46 (m, 2H), 7.42 (t, J = 8.0 Hz, 2H), 7.37-7.31 (m, 4H), 7.31-7.27 (m, 1H), 6.22 (s, 1H), 3.97 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 197.9, 167.2, 139.4, 138.5, 136.6, 135.5, 133.3, 131.5, 130.7, 129.8, 129.2, 129.0, 128.9, 128.7, 128.22, 128.19, 127.6, 127.4, 125.6, 59.5, 52.2; HRMS (ESI) m/z calcd for C26H21O3 + [M+H]+: 381.1485 found 381.1473。
1H NMR (600 MHz, CDCl3) δ 8.00 (dd, J = 7.2, 1.2 Hz, 2H), 7.51 (tt, J = 7.2, 1.2 Hz, 1H), 7.41 (t, J = 7.8 Hz, 2H), 7.34-7.30 (m, 4H), 7.30-7.22 (m, 6H), 6.04 (s, 1H); 13C NMR (150 MHz, CDCl3) δ 198.2, 139.1, 136.8, 133.0, 129.1, 128.9, 128.7, 128.6, 127.1, 59.4; HRMS (ESI) m/z calcd for C20H17O+ [M+H]+: 273.1274 found 273.1265。
1H NMR (400 MHz, CDCl3) δ 8.00 (d, J = 7.6 Hz, 2H), 7.50 (t, J = 7.2 Hz, 1H), 7.40 (t, J = 8.0 Hz, 2H), 7.35-7.28 (m, 2H), 7.28-7.22 (m, 3H), 7.19 (d, J = 9.2 Hz, 2H), 6.86 (d, J = 8.4 Hz, 2H), 5.99 (s, 1H), 3.77 (s, 3H); 13C NMR (150 MHz, CDCl3) δ 198.4, 158.6, 139.4, 136.8, 133.0, 131.1, 130.1, 129.0, 128.9, 128.7, 128.6, 127.0, 114.1, 58.6, 55.2; HRMS (ESI) m/z calcd for C21H19O2 +[M+H]+: 303.1380 found 303.1371。
1H NMR (400 MHz, CDCl3) δ 8.01-7.97 (m, 4H), 7.53 (tt, J = 7.6, 1.2 Hz, 1H), 7.42 (t, J = 7.6 Hz, 2H), 7.36-7.31 (m, 4H), 7.29-7.26 (m, 3H), 6.08 (s, 1H), 3.89 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 197.5, 166.8, 144.3, 138.2, 136.5, 133.3, 129.9, 129.2, 129.1, 128.9, 128.7, 127.5, 59.3, 52.1; HRMS (ESI) m/z calcd for C22H19O3 +[M+H]+: 331.1329 found 331.1319。
1H NMR (400 MHz, CDCl3) δ 8.03 (d, J = 7.6 Hz, 2H), 7.58-7.50 (m, 5H), 7.45-7.38 (m, 4H), 7.37-7.30 (m, 7H), 7.30-7.26 (m, 1H), 6.08 (s, 1H); 13C NMR (100 MHz, CDCl3) δ 198.2, 140.7, 140.0, 139.0, 138.1, 136.8, 133.1, 129.5, 129.1, 129.0, 128.8, 128.7, 128.6, 127.4, 127.3, 127.2, 127.1, 59.1; HRMS (ESI) m/z calcd for C26H21O+[M+H]+: 349.1587 found 349.1579。
1H NMR (600 MHz, CDCl3) δ 7.98 (dd, J = 8.4, 1.2 Hz, 2H), 7.79-7.77 (m, 3H), 7.72 (s, 1H), 7.45-7.39 (m, 4H), 7.34 (t, J = 7.8 Hz, 2H), 4.84 (q, J = 6.6 Hz, 1H), 1.61 (d, J = 6.6 Hz, 3H); 13C NMR (150 MHz, CDCl3) δ 200.2, 139.0, 136.4, 133.6, 132.8, 132.3, 128.8, 128.5, 127.7, 127.6, 126.4, 126.1, 125.9, 125.8, 48.0, 19.5; HRMS (ESI) m/z calcd for C19H16NaO+ [M+Na]+: 283.1093 found 283.1085。
1H NMR (400 MHz, CDCl3) δ 8.01 (dd, J = 8.4, 1.6 Hz, 2H), 7.80-7.75 (m, 4H), 7.53-7.35 (m, 6H), 4.38 (d, J = 10.4 Hz, 1H), 2.77-2.65 (m, 1H), 1.06 (d, J = 6.4 Hz, 3H), 0.77 (d, J = 6.4 Hz, 3H); 13C NMR (150 MHz, CDCl3) δ 200.5, 137.6, 136.1, 133.5, 132.8, 132.5, 128.5, 128.4, 127.74, 127.69, 127.6, 126.7, 126.0, 125.7, 61.4, 31.9, 22.0, 20.6; HRMS (ESI) m/z calcd for C21H21O+ [M+H]+: 289.1587 found 289.1578。
1H NMR (600 MHz, CDCl3) δ 8.06 (d, J = 9.0 Hz, 2H), 7.91-7.85 (m, 2H), 7.78 (d, J = 8.4 Hz, 1H), 7.51-7.46 (m, 2H), 7.42 (t, J = 7.8 Hz, 1H), 7.35 (d, J = 6.6 Hz, 1H), 6.95 (d, J = 9.0 Hz, 2H), 4.69 (s, 2H), 3.87 (s, 3H); 13C NMR (150 MHz, CDCl3) δ 196.2, 163.6, 133.9, 132.3, 131.7, 130.8, 129.8, 128.8, 127.9, 127.7, 126.3, 125.7, 125.5, 123.9, 113.8, 55.5, 42.8; HRMS (ESI) m/z calcd for C19H17O2 +[M+H]+: 277.1223 found 277.1213。
1H NMR (600 MHz, CDCl3) δ 7.98 (d, J = 8.4 Hz, 2H), 7.89-7.84 (m, 2H), 7.78 (d, J = 8.4 Hz, 1H), 7.50-7.46 (m, 2H), 7.42 (dd, J = 8.4, 7.2 Hz, 1H), 7.35 (d, J = 7.2 Hz, 1H), 7.27 (d, J = 8.4 Hz, 2H), 4.71 (s, 2H), 2.42 (s, 3H); 13C NMR (150 MHz, CDCl3) δ 197.3, 144.1, 134.2, 133.9, 132.2, 131.6, 129.4, 128.8, 128.6, 127.9, 127.8, 126.3, 125.7, 125.4, 123.9, 43.0, 21.7; HRMS (ESI) m/z calcd for C19H17O+[M+H]+: 261.1274 found 261.1268。
1H NMR (600 MHz, CDCl3) δ 8.00 (d, J = 9.0 Hz, 2H), 7.94 (dd, J = 7.2, 2.4 Hz, 1H), 7.85 (dd, J = 7.2, 2.4 Hz, 1H), 7.76 (d, J = 7.8 Hz, 1H), 7.50-7.45 (m, 2H), 7.41 (t, J =7.8 Hz, 1H), 7.36 (d, J = 6.6 Hz, 1H), 6.66 (d, J = 9.0 Hz, 2H), 4.65 (s, 2H), 3.06 (s, 6H). 13C NMR (150 MHz, CDCl3) δ 195.7, 153.4. 133.8, 132.5, 132.3, 130.8, 128.7, 127.8, 127.5, 126.1, 125.6, 125.5, 124.7, 124.1, 110.7, 42.4, 40.0; HRMS (ESI) m/z calcd for C20H20NO+ [M+H]+: 290.1539 found 290.1529。
1H NMR (600 MHz, CDCl3) δ 7.93 (d, J = 8.4 Hz, 1H), 7.88 (dd, J = 7.2, 2.4 Hz, 1H), 7.80 (d, J = 8.4 Hz, 1H), 7.53-7.47 (m, 2H), 7.43 (dd, J = 8.4, 7.2 Hz, 1H), 7.38 (d, J = 7.2 Hz, 1H), 7.31 (s, 2H), 4.70 (s, 2H), 3.91 (s, 3H), 3.84 (s, 6H); 13C NMR (150 MHz, CDCl3) δ 196.4, 153.0, 142.6, 133.9, 132.1, 131.8, 131.5, 128.9, 127.90, 127.85, 126.4, 125.8, 125.5, 123.7, 106.0, 60.9, 56.2, 43.2; HRMS (ESI) m/z calcd for C21H21O4 +[M+H]+: 337.1434 found 337.1424。
1H NMR (600 MHz, CDCl3) δ 8.12-8.08 (m, 2H), 7.89-7.85 (m, 2H), 7.80 (d, J = 8.4 Hz, 1H), 7.52-7.47 (m, 2H), 7.43 (dd, J = 7.8, 6.6 Hz, 1H), 7.35 (d, J = 7.2 Hz, 1H), 7.17-7.12 (m, 2H), 4.71 (s, 2H); 13C NMR (150 MHz, CDCl3) δ 196.1, 165.8 (d, JCF = 256.4 Hz), 133.9, 133.1, 132.2, 131.2 (d, JCF = 10.1 Hz), 131.1, 128.6, 127.98, 127.95, 126.4, 125.8, 125.5, 123.7, 115.8 (d, JCF = 23.1 Hz), 43.1; HRMS (ESI) m/z calcd for C18H14FO+ [M+H]+: 265.1023 found 265.1016。
1H NMR (400 MHz, CDCl3) δ8.16 (d, J = 8.4 Hz, 2H), 7.90-7.84 (m, 2H), 7.81 (d, J = 8.4 Hz, 1H), 7.74 (d, J = 8.4 Hz, 2H), 7.53-7.49 (m, 2H), 7.44 (dd, J = 8.4, 7.2 Hz, 1H), 7.36 (d, J = 7.2 Hz, 1H), 4.76 (s, 2H); 13C NMR (150 MHz, CDCl3) δ 196.7, 139.3, 134.4 (q, JCF = 33.2 Hz), 133.9, 132.1, 130.5, 128.9, 128.8, 128.2, 128.0, 126.5, 125.8 (q, JCF = 2.9 Hz), 125.5, 123.6, 123.5 (q, JCF= 273.6 Hz), 44.4; HRMS (ESI) m/z calcd for C19H14F3O+[M+H]+: 315.0991 found 315.0981。
1H NMR (600 MHz, CDCl3) δ 9.31 (d, J = 1.2 Hz, 1H), 8.78 (dd, J = 7.2, 1.8 Hz, 1H), 8.28 (dt, J = 8.4, 1.8 Hz, 1H), 7.89-7.85 (m, 2H), 7.80 (d, J = 7.8 Hz, 1H), 7.53-7.47 (m, 2H), 7.44-7.38 (m, 2H), 7.37 (d, J = 7.2 Hz, 1H), 4.73 (s, 2H); 13C NMR (150 MHz, CDCl3) δ 196.5, 153.6, 149.9, 135.8, 133.9, 132.1, 131.9, 130.3, 128.9, 128.2, 128.1, 126.5, 125.8, 125.4, 123.7, 123.6, 43.5; HRMS (ESI) m/z calcd for C17H14NO+[M+H]+: 248.1070 found 248.1064。
1H NMR (400 MHz, CDCl3) δ 7.99 (d, J = 8.0 Hz, 1H), 7.85 (dd, J = 7.2, 2.0 Hz, 1H), 7.78 (dd, J = 7.2, 2.4 Hz, 1H), 7.58 (dd, J = 2.0, 0.8 Hz, 1H), 7.53-7.40 (m, 4H), 7.22 (d, J = 3.6 Hz, 1H), 6.54 (dd, J = 3.6, 2.0 Hz, 1H), 4.59 (s, 2H); 13C NMR (100 MHz, CDCl3) δ 186.5, 152.4, 146.4, 133.8, 132.2, 130.6, 128.7, 128.2, 127.9, 126.3, 125.7, 125.4, 117.7, 112.4, 43.0; HRMS (ESI) m/z calcd for C16H13O2 +[M+H]+: 237.0910 found 237.0904。
1H NMR (600 MHz, CDCl3) δ 7.97 (d, J = 7.8 Hz, 1H), 7.86 (dd, J = 7.8, 1.8 Hz, 1H), 7.84 (dd, J = 4.2, 1.2 Hz, 1H), 7.80 (m, 1H), 7.64 (dd, J = 4.8, 1.2 Hz, 1H), 7.53-7.46 (m, 2H), 7.45-7.41 (m, 2H), 7.12 (dd, J = 4.8, 4.2 Hz, 1H), 4.65 (s, 2H); 13C NMR (150 MHz, CDCl3) δ 190.4, 143.8, 133.9, 133.9, 132.4, 132.2, 130.9, 128.7, 128.1, 128.0, 126.4, 125.8, 125.4, 123.9, 44.1; HRMS (ESI) m/z calcd for C16H13OS+[M+H]+: 253.0682 found 253.0672。
1H NMR (600 MHz, CDCl3) δ: 7.99 (d, J = 7.8 Hz, 1H), 7.84 (dd, J = 7.2, 2.4 Hz, 1H), 7.76 (d, J = 7.8 Hz, 1H), 7.50-7.43 (m, 2H), 7.43-7.38 (m, 2H), 7.28 (t, J = 1.8 Hz, 1H), 6.66 (dd, J = 3.0, 1.8 Hz, 1H), 6.56 (t, J = 2.4 Hz, 1H), 4.47 (s, 2H), 3.65 (s, 3H); 13C NMR (150 MHz, CDCl3) δ: 192.8, 133.8, 132.4, 132.3, 128.6, 127.8, 127.5, 126.9, 126.1, 125.6, 125.4, 124.2, 123.2, 109.8, 44.3, 36.6; HRMS (ESI) m/z calcd for C17H16NO+ [M+H]+: 250.1226 found 250.1220。
1H NMR (400 MHz, CDCl3) δ 8.43-8.39 (m, 1H), 8.05-8.00 (m, 1H), 7.88-7.84 (m, 1H), 7.81 (s, 1H), 7.78 (dd, J = 6.4, 3.2 Hz, 1H), 7.50-7.40 (m, 4H), 7.35-7.27 (m, 3H), 4.61 (s, 2H), 3.81 (s, 3H); 13C NMR (150 MHz, CDCl3) δ 192.6, 137.4, 135.5, 133.9, 132.5, 132.4, 128.7, 127.8, 127.6, 126.6, 126.2, 125.7, 125.5, 124.1, 123.5, 122.8, 122.7, 116.2, 109.6, 44.6, 33.5; HRMS (ESI) m/z calcd for C21H18NO+[M+H]+: 300.1383 found 300.1372。
1H NMR (600 MHz, CDCl3) δ 7.84 (dd, J = 7.8, 1.8 Hz, 1H), 7.76 (d, J = 8.4 Hz, 1H), 7.73 (dd, J = 7.8, 1.8 Hz, 1H), 7.49-7.43 (m, 2H), 7.40 (dd, J = 8.4, 7.2 Hz, 1H), 7.25 (d, 6.6 Hz, 1H), 4.26 (s, 2H), 1.30 (s, 9H); 13C NMR (150 MHz, CDCl3) δ 212.6, 133.8, 132.4, 131.6, 128.7, 127.9, 127.6, 126.0, 125.5, 125.3, 123.7, 44.7, 41.0, 26.8; HRMS (ESI) m/z calcd for C16H19O+ [M+H]+: 227.1430 found 227.1422。
1H NMR (600 MHz, CDCl3) δ 7.82-7.76 (m, 3H), 7.63 (s, 1H), 7.46-7.41 (m, 2H), 7.31 (dd, J = 8.4, 1.8 Hz, 1H), 3.96 (s, 2H), 1.23 (s, 9H); 13C NMR (150 MHz, CDCl3) δ 212.9, 133.4, 132.5, 132.3, 128.1, 127.9, 127.8, 127.61, 127.57, 125.9, 125.5, 44.7, 43.5, 26.5; HRMS (ESI) m/z calcd for C16H18NaO+[M+Na]+: 249.1250 found 249.1241。
1H NMR (400 MHz, CDCl3) δ 8.31 (dd, J = 7.2, 1.6 Hz, 1H), 8.05 (dd, J = 8.8 Hz, 2H), 7.82 (dd, J = 7.2, 1.6 Hz, 1H), 7.53-7.44 (m, 2H), 7.25 (d, J = 8.0 Hz, 1H), 6.94 (d, J = 8.8 Hz, 2H), 6.76 (d, J = 8.0 Hz, 1H), 4.60 (s, 2H), 3.98 (s, 3H), 3.86 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 196.6, 163.5, 154.9, 133.0, 130.8, 129.8, 127.7, 126.7, 126.0, 125.0, 123.7, 123.6, 122.6, 113.8, 103.4, 55.5, 42.4; HRMS (ESI) m/z calcd for C20H19O3 + [M+H]+: 307.1329 found 307.1320。
1H NMR (600 MHz, CDCl3) δ 8.92 (dd, J = 4.2, 1.8 Hz, 1H), 8.25 (d, J = 8.4 Hz, 1H), 8.08-8.04 (m, 3H), 7.67 (dd, J = 8.4, 7.2 Hz, 1H), 7.44 (d, J = 7.2 Hz, 1H), 7.41 (dd, J = 8.4, 4.2 Hz, 1H), 6.97 (d, J = 9.0 Hz, 2H), 4.70 (s, 2H), 3.89 (s, 3H); 13C NMR (150 MHz, CDCl3) δ 195.5, 163.8, 150.1, 148.7, 132.6, 132.1, 130.8, 129.4, 129.2, 129.0, 128.4, 127.6, 121.1, 113.9, 55.5, 42.2; HRMS (ESI) m/z calcd for C18H16NO2 +[M+H]+: 278.1176 found 278.1170。
1H NMR (600 MHz, CDCl3) δ 8.90 (dd, J = 4.2, 1.8 Hz, 1H), 8.16-8.12 (m, 3H), 7.75 (dd, J = 8.4, 1.2 Hz, 1H), 7.65 (d, J = 7.2 Hz, 1H), 7.50 (dd, J = 8.4, 7.2 Hz, 1H), 7.40 (dd, J = 9.0, 4.2 Hz, 1H), 6.91 (d, J = 9.0 Hz, 2H), 4.95 (s, 2H), 3.85 (s, 3H); 13C NMR (150 MHz, CDCl3) δ 197.1, 163.3, 149.6, 146.5, 136.3, 134.5, 131.0, 130.3, 130.1, 128.5, 127.1, 126.3, 121.1, 113.6, 55.4, 40.4; HRMS (ESI) m/z calcd for C18H16NO2 + [M+H]+: 278.1176 found 278.1168。
1H NMR (600 MHz, CDCl3) δ 8.58 (s, 1H), 8.05-8.01 (m, 3H), 7.91 (d, J = 8.4 Hz, 1H), 7.82 (d, J = 9.0 Hz, 1H), 7.76 (s, 1H), 7.46 (dd, J = 8.4, 1.8 Hz, 1H), 6.94 (d, J = 9.0 Hz, 2H), 4.42 (s, 2H), 3.97 (s, 3H), 3.86 (s, 3H); 13C NMR (150 MHz, CDCl3) δ 195.8, 167.2, 163.7, 135.6, 135.3, 131.4, 130.9, 130.8, 129.6, 128.5, 127.92, 127.85, 127.2, 125.5, 113.9, 55.5, 52.2, 45.4; HRMS (ESI) m/z calcd for C21H19O4 +[M+H]+: 337.1434 found 337.1424。
1H NMR (400 MHz, DMSO-d6, 120℃) δ 8.32 (s, 1H), 8.22 (d, J = 8.4 Hz, 1H), 7.49 (d, J = 8.4 Hz, 1H), 7.30-7.17 (m, 7H), 7.15 (d, J = 7.2 Hz, 2H), 6.97 (d, J = 8.0 Hz, 2H), 4.63 (d, J = 16.8 Hz, 1H), 4.21 (d, J = 16.8 Hz, 1H), 4.10 (s, 2H), 3.91 (t, J = 6.4 Hz, 1H), 3.87 (s, 3H), 3.54 (s, 3H), 3.30 (dd, J = 14.4, 6.4 Hz, 1H), 3.02 (dd, J = 14.4, 6.4 Hz, 1H), 1.23 (s, 9H); 13C NMR (100 MHz, DMSO-d6, 120℃) δ 191.2, 176.7, 169.8, 137.0, 136.8, 136.2, 135.8, 133.9, 128.51, 128.48, 127.5, 127.0, 126.4, 125.9, 122.2, 121.3, 121.0, 114.8, 109.6, 61.3, 51.6, 50.6, 45.2, 38.1, 34.5, 32.4, 27.7. HRMS (ESI) m/z calcd for C33H37N2O4 [M+H]+: 525.2748 found. 525.2737。
1H NMR (400 MHz, DMSO-d6, 120℃) δ 7.98 (d, J = 8.8 Hz, 2H), 7.30-7.24 (m, 3H), 7.17-7.11 (m, 4H), 7.03-6.94 (m, 4H), 4.63 (d, J = 16.4 Hz, 1H) 4.23 (s, 2H), 4.13 (d, J = 16.4 Hz, 1H), 3.90 (t, J = 7.6 Hz, 1H), 3.84 (s, 3H), 3.54 (s, 3H), 3.28 (dd, J = 14.4, 7.6 Hz, 1H), 3.03 (dd, J = 14.4, 7.6 Hz, 1H), 1.22 (s, 9H); 13C NMR (100 MHz, DMSO-d6, 120℃) δ 195.4, 176.6, 169.8, 162.7, 136.2, 136.0, 133.0, 130.0, 129.2, 128.6, 127.5, 127.0, 126.5, 113.4, 61.2, 54.9, 51.6, 50.6, 43.7, 38.1, 34.4, 27.7. HRMS (ESI) m/z calcd for C31H35NNaO3[M+Na]+: 524.2407 found. 524.2394。
1H NMR (400 MHz, CDCl3) δ 8.00 (d, J = 8.8 Hz, 2H), 7.24 (d, J = 8.0 Hz, 1H), 7.05 (dd, J = 8.0, 2.0 Hz, 1H), 7.00 (d, J = 2.0 Hz, 1H), 6.93 (d, J = 8.8 Hz, 2H) 4.17 (s, 2H), 3.86 (s, 3H), 2.89 (dd, J = 8.8, 4.0 Hz, 2H), 2.50 (dd, J = 19.6, 8.8 Hz, 1H), 2.44-2.36 (m, 1H), 2.28 (td, J = 10.4, 4.0 Hz, 1H), 2.19-1.91 (m, 4H), 1.68-1.35 (m, 6H), 0.90 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 220.9, 196.4, 163.5, 138.2, 136.7, 132.2, 130.9, 129.9, 129.6, 126.8, 125.6, 113.7, 55.4, 50.4, 47.9, 44.7, 44.2, 38.0, 35.8, 31.5, 29.3, 26.4, 25.6, 21.5, 13.8; HRMS (ESI) m/z calcd for C27H31O3[M+H]+: 403.2268 found 403.2257。
各化合物のスペクトルデータは以下のとおりであった。
HRMS (ESI): calculated for C20H17FNaO2[M+Na]+ = 331.1105, found: 331.1099。
実施例2−1で得たニッケル錯体3f及び試験例1で得たニッケル錯体5の結晶をミネラルオイルに浸し、グラスファイバー上に置き、ゴニオメーターであるリガク社製CCD単結晶自動X線構造解析装置「Saturn」(商品名)に移した。グラファイト単色光Mo Kα放射線(λ= 0.71070 Å)を用いた。結果を表12に示す。また、それぞれの熱振動楕円体作画ソフト(ORTEP)による構造を図1〜2に示す。
Claims (14)
- 5員環又は6員環のヘテロ環に、ジアルキルホスフィン及び/又はジシクロアルキルホスフィンが2個置換されたダイホスフィン骨格を有する化合物、又はその塩。
- 一般式(1)において、R1〜R4は同じか又は異なり、それぞれ置換されていてもよいシクロアルキル基である、請求項2に記載の化合物又はその塩。
- カルボニル化合物とフェノール誘導体とのカップリング反応用の触媒を製造するために使用される、請求項1〜3のいずれかに記載の化合物又はその塩。
- 5員環又は6員環のヘテロ環に、ジアルキルホスフィン及び/又はジシクロアルキルホスフィンが2個置換されたダイホスフィン骨格を有し、且つ、該ダイホスフィン骨格が、ニッケル原子に結合している、化合物。
- 一般式(2)において、R1〜R4は同じか又は異なり、それぞれ置換されていてもよいシクロアルキル基である、請求項5又は6に記載の化合物。
- カルボニル化合物とフェノール誘導体とのカップリング反応用の触媒である、請求項5〜7のいずれかに記載の化合物。
- 請求項5〜8のいずれかに記載の化合物の存在下に、カルボニル化合物とフェノール誘導体とをカップリング反応に供する工程を含むことを特徴とする、アリール化カルボニル化合物の製造方法。
- 請求項5〜8のいずれかに記載の化合物の存在下に、カルボニル化合物とフェノール誘導体とを反応させることを特徴とする、カップリング方法。
- カルボニル化合物とフェノール誘導体とをカップリング反応に供する工程を含むアリールカルボニル化合物の製造方法であって、
前記カップリング反応は、単座又は二座のジアルキルホスフィン及び/又はジシクロアルキルホスフィン骨格を有するニッケル化合物の存在下で行う、製造方法。 - カルボニル化合物とフェノール誘導体とを反応させるカップリング方法であって、
前記反応は、単座又は二座のジアルキルホスフィン及び/又はジシクロアルキルホスフィン骨格を有するニッケル化合物の存在下で行う、方法。
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014142721A JP6399540B2 (ja) | 2014-03-11 | 2014-07-10 | 配位子、該配位子を含むニッケル錯体、及び該ニッケル錯体を用いた反応 |
US14/643,365 US20160074853A1 (en) | 2014-03-11 | 2015-03-10 | Ligand, nickel complex comprising the ligand, and reaction using the nickel complex |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014048094 | 2014-03-11 | ||
JP2014048094 | 2014-03-11 | ||
JP2014142721A JP6399540B2 (ja) | 2014-03-11 | 2014-07-10 | 配位子、該配位子を含むニッケル錯体、及び該ニッケル錯体を用いた反応 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2015187092A true JP2015187092A (ja) | 2015-10-29 |
JP6399540B2 JP6399540B2 (ja) | 2018-10-03 |
Family
ID=54429575
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2014142721A Active JP6399540B2 (ja) | 2014-03-11 | 2014-07-10 | 配位子、該配位子を含むニッケル錯体、及び該ニッケル錯体を用いた反応 |
Country Status (2)
Country | Link |
---|---|
US (1) | US20160074853A1 (ja) |
JP (1) | JP6399540B2 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107353312A (zh) * | 2017-07-12 | 2017-11-17 | 四川理工学院 | 一种含dppf骨架和O‑烷基二硫代磷酸配体的[镍铁]氢化酶模型物及其制备方法 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112110801B (zh) * | 2020-10-09 | 2022-07-19 | 浙江工业大学 | 一种γ-芳基取代酮类化合物的合成方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03188091A (ja) * | 1989-12-18 | 1991-08-16 | Fuji Yakuhin Kogyo Kk | 光学活性3,4―ビスホスフィノピロリジン化合物 |
US6133387A (en) * | 1998-11-17 | 2000-10-17 | Nova Chemicals (International) S.A. | Group 8, 9 or 10 olefin copolymerization catalyst |
EP1046647A2 (en) * | 1999-04-22 | 2000-10-25 | Nova Chemicals (International) S.A. | Group 8,9 or 10 transition metal catalyst for olefin polymerization |
US20100093920A1 (en) * | 2008-10-01 | 2010-04-15 | Pawlow James H | Nickel catalyst system for the preparation of high cis polybutadiene |
-
2014
- 2014-07-10 JP JP2014142721A patent/JP6399540B2/ja active Active
-
2015
- 2015-03-10 US US14/643,365 patent/US20160074853A1/en not_active Abandoned
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03188091A (ja) * | 1989-12-18 | 1991-08-16 | Fuji Yakuhin Kogyo Kk | 光学活性3,4―ビスホスフィノピロリジン化合物 |
US6133387A (en) * | 1998-11-17 | 2000-10-17 | Nova Chemicals (International) S.A. | Group 8, 9 or 10 olefin copolymerization catalyst |
EP1046647A2 (en) * | 1999-04-22 | 2000-10-25 | Nova Chemicals (International) S.A. | Group 8,9 or 10 transition metal catalyst for olefin polymerization |
US20100093920A1 (en) * | 2008-10-01 | 2010-04-15 | Pawlow James H | Nickel catalyst system for the preparation of high cis polybutadiene |
Non-Patent Citations (4)
Title |
---|
AI, PENGFEI, ET AL., CHEMICAL COMMUNICATIONS, vol. 2014, 50(1), JPN6018003520, 24 October 2013 (2013-10-24), pages pp. 103-105 * |
AL-BENNA, SARAH, ET AL., JOURNAL OF THE CHEMICAL SOCIETY, DALTON TRANSACTIONS, vol. 23, JPN7018000325, 2000, pages pp. 4247-4257 * |
KINTING, ANNEGRET, ET AL., JOURNAL OF ORGANOMETALLIC CHEMISTRY, vol. 370, JPN6018003519, 1989, pages pp. 351-356 * |
MUTO, KEI, ET AL., JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 135, JPN6018003518, 2013, pages pp. 16384-16387 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107353312A (zh) * | 2017-07-12 | 2017-11-17 | 四川理工学院 | 一种含dppf骨架和O‑烷基二硫代磷酸配体的[镍铁]氢化酶模型物及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
JP6399540B2 (ja) | 2018-10-03 |
US20160074853A1 (en) | 2016-03-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Xu et al. | Cu (OAc) 2· H2O-catalyzed N-arylation of nitrogen-containing heterocycles | |
JP6290788B2 (ja) | 4−クロロ−2−フルオロ−3−置換−フェニルボロン酸ピナコールエステルの形成方法およびその使用方法 | |
Chen et al. | Acetonitrile-dependent oxyphosphorylation: A mild one-pot synthesis of β-ketophosphonates from alkenyl acids or alkenes | |
Yang et al. | Mn-Catalyzed 1, 6-conjugate addition/aromatization of para-quinone methides | |
Harinath et al. | Aluminium complex-catalysed hydroboration of alkenes and alkynes | |
CN106146454B (zh) | Negishi偶联制备多氟联芳烃类化合物的方法 | |
JP6393322B2 (ja) | 新規なキラル窒素−リン配位子及びアルケン類の不斉水素化のためのその使用 | |
JPWO2008093637A1 (ja) | 有機トリオールボレート塩を含んでなる有機合成反応用試薬 | |
CN101671365A (zh) | 手性螺环胺基膦配体化合物与合成方法及其应用 | |
JPWO2014136795A1 (ja) | 配位子、その配位子を含む金属錯体、及びその金属錯体を用いた反応 | |
Ling et al. | Copper-catalyzed N-alkylation of indoles by N-tosylhydrazones | |
JP6399540B2 (ja) | 配位子、該配位子を含むニッケル錯体、及び該ニッケル錯体を用いた反応 | |
Wen et al. | Iron-catalyzed decarbonylative borylation enables the one-pot diversification of (Hetero) Aryl and alkyl carboxylic acids | |
Pandiri et al. | Synthesis of quinolinyl-based pincer copper (II) complexes: an efficient catalyst system for Kumada coupling of alkyl chlorides and bromides with alkyl Grignard reagents | |
JP4864342B2 (ja) | ビアリール化合物の製造方法 | |
JP5915607B2 (ja) | チオノカルボン酸アリールエステルの製造方法 | |
WO2013028132A9 (en) | Chiral phosphines for palladium-catalyzed asymmetric alpha-arylation of ester enolates to produce tertiary stereocenters in high enantioselectivity | |
Pal et al. | One-pot synthesis of dimerized arenes and heteroarenes under mild conditions using Co (I) as an active catalyst | |
JP2017519755A (ja) | ボリル化アーレンを製造する方法 | |
Zhang et al. | Lanthanide-catalyzed deamidative cyclization of secondary amides and ynones through tandem C–H and C–N activation | |
Li et al. | Nickel-catalyzed regioselective arylation of aromatic amides with aryl iodides enabled by an N, O-bidentate directing group | |
Toffano et al. | Synthesis of Enantiopure 1‐r‐Aryl‐2‐c, 5‐t‐diphenylphospholane Oxides and Boranes by Pd‐Catalyzed C–P Bond Formation | |
Bush et al. | Development of a palladium catalyzed addition of boronic acids to alkynyl esters: synthesis of trisubstituted olefins as single isomers | |
CN114907404A (zh) | 5-(2-(二取代膦基)苯基)-1-烷基-1h-吡唑膦配体及其制备方法和应用 | |
JPWO2016027809A1 (ja) | クロスカップリング方法、及び該クロスカップリング方法を用いた有機化合物の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20170523 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20180131 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20180206 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20180406 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20180731 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20180829 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6399540 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
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 |