CN112824373A - Method for preparing chiral amine by iridium-catalyzed asymmetric hydrogenation of imine - Google Patents
Method for preparing chiral amine by iridium-catalyzed asymmetric hydrogenation of imine Download PDFInfo
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- CN112824373A CN112824373A CN201911147145.3A CN201911147145A CN112824373A CN 112824373 A CN112824373 A CN 112824373A CN 201911147145 A CN201911147145 A CN 201911147145A CN 112824373 A CN112824373 A CN 112824373A
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- iridium
- imine
- chiral amine
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- asymmetric hydrogenation
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- 150000002466 imines Chemical class 0.000 title claims abstract description 39
- 238000000034 method Methods 0.000 title claims abstract description 23
- 150000001412 amines Chemical class 0.000 title claims abstract description 19
- 238000009876 asymmetric hydrogenation reaction Methods 0.000 title claims abstract description 18
- 229910052741 iridium Inorganic materials 0.000 claims abstract description 28
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000003054 catalyst Substances 0.000 claims abstract description 27
- VURFVHCLMJOLKN-UHFFFAOYSA-N diphosphane Chemical compound PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000003446 ligand Substances 0.000 claims abstract description 20
- 238000002360 preparation method Methods 0.000 claims abstract description 10
- 238000011065 in-situ storage Methods 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 claims description 28
- -1 amine compound Chemical class 0.000 claims description 21
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 17
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 239000000758 substrate Substances 0.000 claims description 10
- 229910052717 sulfur Inorganic materials 0.000 claims description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 239000007810 chemical reaction solvent Substances 0.000 claims description 6
- 125000004185 ester group Chemical group 0.000 claims description 6
- 125000000524 functional group Chemical group 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 4
- BXMJNGVLZAWGJH-UHFFFAOYSA-N [Ir].C1CCC=CC=CC1 Chemical compound [Ir].C1CCC=CC=CC1 BXMJNGVLZAWGJH-UHFFFAOYSA-N 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000001624 naphthyl group Chemical group 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 238000010898 silica gel chromatography Methods 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims description 2
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 229930192474 thiophene Chemical group 0.000 claims description 2
- 238000001291 vacuum drying Methods 0.000 claims description 2
- JJVKJJNCIILLRP-UHFFFAOYSA-N 2-ethyl-6-methylaniline Chemical compound CCC1=CC=CC(C)=C1N JJVKJJNCIILLRP-UHFFFAOYSA-N 0.000 abstract description 4
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- 239000002243 precursor Substances 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- 239000012454 non-polar solvent Substances 0.000 abstract 1
- 239000002798 polar solvent Substances 0.000 abstract 1
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 24
- 238000004128 high performance liquid chromatography Methods 0.000 description 24
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
- 238000005160 1H NMR spectroscopy Methods 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 238000005481 NMR spectroscopy Methods 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000001514 detection method Methods 0.000 description 6
- YMWUJEATGCHHMB-DICFDUPASA-N dichloromethane-d2 Chemical compound [2H]C([2H])(Cl)Cl YMWUJEATGCHHMB-DICFDUPASA-N 0.000 description 6
- 238000004817 gas chromatography Methods 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- 238000004440 column chromatography Methods 0.000 description 5
- 208000012839 conversion disease Diseases 0.000 description 5
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 4
- WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 description 3
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 3
- 238000004679 31P NMR spectroscopy Methods 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 238000006555 catalytic reaction Methods 0.000 description 3
- XGRJZXREYAXTGV-UHFFFAOYSA-N chlorodiphenylphosphine Chemical compound C=1C=CC=CC=1P(Cl)C1=CC=CC=C1 XGRJZXREYAXTGV-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- CUZLJOLBIRPEFB-UHFFFAOYSA-N 1-methoxypropan-2-one Chemical compound COCC(C)=O CUZLJOLBIRPEFB-UHFFFAOYSA-N 0.000 description 1
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 1
- 239000004287 Dehydroacetic acid Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000005617 S-Metolachlor Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- GZNDMPGAAUXELR-UHFFFAOYSA-N [Cl-].CC=1C=C(C=C(C=1)C)[PH2+]C1=CC(=CC(=C1)C)C Chemical compound [Cl-].CC=1C=C(C=C(C=1)C)[PH2+]C1=CC(=CC(=C1)C)C GZNDMPGAAUXELR-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- OEYYXYIGOCGWMI-UHFFFAOYSA-N bis[3,5-bis(trifluoromethyl)phenyl]phosphane hydrochloride Chemical compound Cl.FC(F)(F)C1=CC(C(F)(F)F)=CC(PC=2C=C(C=C(C=2)C(F)(F)F)C(F)(F)F)=C1 OEYYXYIGOCGWMI-UHFFFAOYSA-N 0.000 description 1
- 230000002153 concerted effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 235000019258 dehydroacetic acid Nutrition 0.000 description 1
- JEQRBTDTEKWZBW-UHFFFAOYSA-N dehydroacetic acid Chemical compound CC(=O)C1=C(O)OC(C)=CC1=O JEQRBTDTEKWZBW-UHFFFAOYSA-N 0.000 description 1
- 229940061632 dehydroacetic acid Drugs 0.000 description 1
- PGRHXDWITVMQBC-UHFFFAOYSA-N dehydroacetic acid Natural products CC(=O)C1C(=O)OC(C)=CC1=O PGRHXDWITVMQBC-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
Classifications
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- 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
-
- 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
-
- 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
-
- 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
- B01J2231/60—Reduction reactions, e.g. hydrogenation
- B01J2231/64—Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
- B01J2231/641—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
-
- 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
- B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
- B01J2531/0202—Polynuclearity
- B01J2531/0205—Bi- or polynuclear complexes, i.e. comprising two or more metal coordination centres, without metal-metal bonds, e.g. Cp(Lx)Zr-imidazole-Zr(Lx)Cp
-
- 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
- B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
- B01J2531/0225—Complexes comprising pentahapto-cyclopentadienyl analogues
-
- 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
- B01J2531/82—Metals of the platinum group
- B01J2531/827—Iridium
-
- 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
- B01J2531/842—Iron
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention discloses a method for preparing chiral amine by iridium-catalyzed asymmetric hydrogenation of imine. The iridium catalyst adopted by the method is generated in situ in various polar and nonpolar solvents by a metal iridium precursor and a chiral diphosphine ligand, and the dosage (by mol) of the catalyst is as follows: the raw material imine/catalyst (S/C) is equal to 300000-1000000. The ligand of the invention has simple preparation, low catalyst consumption and simple and convenient operation, can realize continuous operation, is suitable for preparing chiral amine on a large scale, and has an enantiomeric excess value (ee value) of the product of more than 80 percent. The invention has low consumption of the synthetic catalyst of the key intermediate of the metolachlor, the 2-ethyl-6-methylaniline/the catalyst (S/C) is 500000, the yield can reach 95 percent, the enantioselectivity is 91 percent, and the invention has good industrial application range.
Description
Technical Field
The invention belongs to the field of organic synthesis, and particularly relates to a method for preparing chiral amine by catalyzing asymmetric hydrogenation of imine with iridium/chiral diphosphine ligand.
Background
Chiral amine compounds are organic synthetic building blocks with important application values, and are widely applied to the synthesis of biology, agriculture and pharmaceutical preparations. The efficient preparation of highly optical homochiral amine compounds has also become a research hotspot for organic chemists. Among many synthetic strategies, the asymmetric hydrogenation reaction of imine is undoubtedly the simplest and most efficient method, and the catalytic system mainly includes three types of transition metal catalysis, organic catalysis and metal-organic concerted catalysis [ (a) Li, w ]; zhang, x.top.curr.chem.2013,343, 103-144; (b) verendel, j.j.; pamies, o.; di guez, M.; andersson, P.G.chem.Rev.2014,114, 2130-2169; (c) etayo, p.; Vidal-Ferran, A.chem.Soc.Rev.2013,42, 728-754; (d) xie, j. -h.; zhu, s. -f.; zhou, q. — l.chem.rev.2011,111, 1713-1760; (e) faisca Phillips, a.m.; pomberiro, a.j.l.org.biomol.chem.2017,15, 2307-; (f) rueping, m.; dufour, j.; schoepke, F.R.Green chem.2011,13, 1084-1105; (g) tang, w.; xiao, j.synthesis 2014,46, 1297-1302; (h) du, z.; shao, Z.chem.Soc.Rev.2013,42, 1337-1378; (i) stegbauer, l.; sladojevich, F.; dixon, d.j.chem.sci.2012,3,942-958 ]. However, these catalytic systems still have many disadvantages and limitations, such as large amount of catalyst, relatively low S/C, narrow substrate range, and harsh reaction conditions. The subject group of the inventors has been devoted for many years to the design and development of asymmetric hydrogenation catalytic systems and research of their application in the synthesis of the broad-spectrum herbicide (S) -metolachlor. The key step of the existing industrial production technology is to realize the oriented synthesis of the (S) -metolachlor intermediate by asymmetrically hydrogenating and reducing (2-methyl-6-ethyl aniline) -imine, but chiral amine with 76% ee can only be obtained, the synthesis of the used ligand is difficult, and the requirement of the reaction condition on equipment is high. Therefore, the development of novel, efficient and universal chiral catalysts becomes the key to solve the difficulties of chiral amine synthesis and practical application.
Disclosure of Invention
Aiming at the defects in the prior art, the invention provides a method for preparing chiral amine by catalyzing asymmetric hydrogenation of imine by an iridium/chiral diphosphine ligand, and the method has the advantages of cheap and easily prepared catalyst, high activity, high stereoselectivity, greenness, simplicity and convenience and the like.
The technical scheme of the invention comprises the following specific steps:
(1) preparation of chiral iridium catalyst: under the protection of nitrogen, stirring the iridium-cyclooctadiene complex and chiral diphosphine ligand in a reaction medium for 2 hours to prepare a chiral iridium catalyst by in-situ coordination;
(2) preparation of chiral amine compound: dissolving substrate imine in a reaction medium, adding the substrate imine into the stirred chiral iridium catalyst solution, placing the solution in a high-pressure reaction kettle, performing hydrogen replacement for 3 times, introducing hydrogen to 20-100 bar, and reacting for 1-24 hours at 20-100 ℃; after the reaction is finished, slowly releasing hydrogen, concentrating under reduced pressure until no solvent exists basically, separating by silica gel column chromatography, concentrating under reduced pressure, and drying under vacuum to obtain chiral amine compound;
the imine (1) and the chiral amine compound (2) have the following structures:
in the formula: r1Is C1~C10Alkyl radicals such as CH3、CH3CH2Etc. C3~C12Cycloalkyl radicals such as cyclopentyl, cyclohexyl, etc., or C containing one or more functional groups of N, S, O, P1~C10Alkyl such as methoxymethyl, ethoxymethyl, etc., or C containing one or more functional groups of N, S, O, P3~C10Cycloalkyl groups such as 2-tetrahydrofuryl, 4-tetrahydrofuryl, etc.; or aryl or the like C6~C30Aromatic groups such as phenyl, 4-methoxyphenyl, etc., which may or may not contain N, S, O, P, etc.; or ester groups such as COOCH3、COOCH2CH3Etc.; r2Is H, C1~C40Alkyl or aryl within; ar is C such as phenyl, 2-substituted, 3-substituted, 4-substituted, 2, 6-disubstituted, 2,4, 6-trisubstituted aryl, etc6~C30Aromatic groups containing or not containing N, S, O, P functional groups such as 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 2-methyl-6-ethylphenyl, thiophene, etc.
The iridium-cyclooctadiene complex is [ Ir (COD) Cl]2、Ir(COD)2BARF or Ir (COD)2BF4。
The structural general formula of the chiral diphosphine ligand is as follows:
wherein: r is C1-C40 alkyl and C3-C12 cycloalkyl, phenyl and substituted phenyl, naphthyl and substituted naphthyl, contains one or more than two five-membered or six-membered heterocyclic aromatic groups of oxygen, sulfur and nitrogen atoms, and has 1-5 substituents of C1-C40 alkyl, C1-C40 alkoxy, halogen, nitro, ester group or cyano;
ar is one of phenyl or substituted phenyl, the substituent is one or more of C1-C40 alkyl, C1-C40 alkoxy, halogen, nitro, ester group or cyano, and the number of the substituents is 1-5.
The concentration of iridium in the reaction system is 0.0001-0.01 mol/L, and the molar ratio of the chiral diphosphine ligand to iridium is 1-5: 1;
the molar ratio of the imine substrate to the iridium catalyst is 300000-500000: 1;
the solvent is at least one of dichloromethane, 1, 2-dichloroethane or toluene;
the hydrogen pressure is 20-100 bar;
the reaction temperature is 20-100 ℃;
the reaction time is 1-24 hours.
In order to achieve the purpose, the technical scheme of the invention is as follows:
in the above reaction formula, the general formula (1) represents a reaction substrate imine, and the general formula (2) represents a chiral amine compound.
The invention has the beneficial effects that:
compared with other methods for synthesizing chiral amine, the method has the advantages that the preparation of the ligand is simple, the dosage of the catalyst is low, and the dosage (by mol) of the catalyst is as follows: the imine/catalyst (S/C) as the raw material is equal to 300000-1000000, the operation is simple and convenient, the continuous operation can be realized, the method is suitable for preparing the chiral amine on a large scale, and the enantiomeric excess value (ee value) of the product reaches more than 80%. The invention has low consumption of the synthetic catalyst of the key intermediate of the metolachlor, the 2-ethyl-6-methylaniline/the catalyst (S/C) is 500000, the yield can reach 95 percent, the enantioselectivity is 91 percent, and the invention has good industrial application range.
Detailed Description
The following examples further illustrate the invention but are not intended to limit the invention thereto. NMR was measured by Bruker NMR and High Performance Liquid Chromatography (HPLC) was measured by Agilent1100 series HPLC. GC analysis conditions were as follows: SE-54, injection port temperature: 250 ℃, detector temperature: column temperature 250 ℃ initial temperature 50 ℃ held for 2 minutes, then 10 degrees/minute to 250 ℃, held for 5 minutes.
The ligand synthesis method related by the invention is shown as the following reaction equation:
example 1
Ligand (R)c,Sp) Preparation of-L1
Under the protection of nitrogen, (R) isc,Sp) -3a (3mmol) and benzimidazole (24mmol) were dissolved in 15mL dehydroacetic acid and heated to 80 ℃ for 8 hours. Cooling, neutralizing with excessive saturated sodium bicarbonate solution, extracting with dichloromethane (3 × 50mL), mixing organic phases, washing with saturated brine, drying over anhydrous sodium sulfate, concentrating under reduced pressure to substantially no solvent, separating with silica gel column chromatography (n-hexane/ethyl acetate/triethylamine: 10/10/1), concentrating under reduced pressure, and vacuum drying to obtain brown crystal (R)c,Sp)-4a。
Under the protection of nitrogen, (R) isc,Sp) -4a (0.5mmol) was dissolved in 15mL of anhydrous ether, 0.47mL of n-BuLi (1.6M n-hexane solution) was slowly added dropwise, the reaction mixture gradually turned into a deep red clear solution, and the reaction was continued for one hour. Then continuously dropwise adding 0.13mL of diphenyl phosphine chloride, reacting for two hours, adding a saturated sodium bicarbonate solution, separating, washing an organic phase with saturated saline solution, drying with anhydrous sodium sulfate, concentrating under reduced pressure until no solvent exists basically, separating by silica gel column chromatography (normal hexane/ethyl acetate: 10/1), and recrystallizing normal hexane to obtain an orange red crystal (R)c,Sp) -L1, yield 50%.
Ligand (R)c,Sp) Structural formula and nmr spectral data of L1 are as follows:
1H NMR(400MHz,CD2Cl2):δ7.64(m,2H),7.38(m,2H),7.08(m,2H),6.95(m,10H),6.83(m,1H),6.61(m,2H),6.36(m,2H),6.06(m,2H),5.46(m,2H),4.58(s,1H),4.19(s,1H),3.66(m,6H),2.50(m,1H),1.12(d,J=6.4Hz,3H),0.01(d,J=6.4Hz,3H);13C NMR(100MHz,CD2Cl2):δ136.3(d,J=9Hz),135.9,135.5,134.3(dd,J=15,21Hz),133.0(d,J=21Hz),129.7(d,J=11Hz),127.9,127.5(d,J=13Hz),137.5(d,J=10Hz),127.0(d,J=8Hz),126.6(d,J=8Hz),126.4(d,J=8Hz),125.3(d,J=6Hz),125.1,120.7,120.1,118.9,111.9,91.7(d,J=27Hz),74.3(d,J=15Hz),71.3(d,J=4Hz),69.8,69.2,68.6,60.2(d,J=20Hz),30.7,21.9,19.3;31P NMR(162MHz,CD2Cl2):δ-36.89(d,J=62.0Hz),-27.94(d,J=62.4Hz).
example 2
Ligand (R)c,Sp) Preparation of-L2
The procedure of example 1 was repeated except that imidazole was used instead of benzimidazole and bis (3, 5-dimethylphenyl) phosphine chloride was used instead of diphenylphosphine chloride in example 1 to obtain an orange-colored solid (R)c,Sp) -L2, yield 49%.
Ligand (R)c,Sp) Structural formula and nmr spectral data of L2 are as follows:
1H NMR(400MHz,CDCl3):δ7.92(m,1H),7.56(s,2H),7.43(d,J=8.4Hz,2H),7.35(s,3H),7.11(m,6H),6.91(d,J=12.4Hz,4H),5.80(m,1H),4.57(s,1H),4.35(s,1H),4.00(s,1H),3.54(s,5H),2.41(m,1H),2.23(s,12H),0.67(d,J=5.2Hz,3H),0.53(d,J=6.4Hz,3H);13C NMR(100MHz,CDCl3):δ138.4,138.0(d,J=9Hz),137.5,135.2(d,J=22Hz),132.7(t,J=17Hz),131(d,J=20Hz),130.3,129.1,128.0(d,J=8Hz),127.8,127.6(d,J=7Hz),121.6(d,J=20Hz),95.44,73.8,73.5,72.6,70.0,69.1,62.3(d,J=11Hz),34.4,21.7,21.4,20.3;31P NMR(162MHz,CDCl3):δ-36.03,-25.34.
example 3
Ligand (R)c,Sp) Preparation of-L3
Orange-colored crystals (R) were obtained in the same manner as in example 1 except that benzimidazole was used instead of benzimidazole and bis (3, 5-bistrifluoromethylphenyl) phosphine chloride was used instead of diphenylphosphine chloride in example 1c,Sp) -L3, yield 47%.
Ligand (R)c,Sp) Structural formula and nmr spectral data of L3 are as follows:
1H NMR(400MHz,CDCl3):δ8.17(m,1H),7.80(m,1H),7.75(m,2H),7.51(m,4H),7.41(m,1H),7.33(m,4H),7.22(m,1H),7.01(m,1H),6.93(m,3H),6.41(t,J=7.4Hz,2H),6.15(m,1H),4.67(s,1H),4.34(s,1H),4.04(s,1H),3.79(s,5H),2.61(m,1H),0.98(d,J=5.2Hz,3H),0.63(d,J=6.6Hz,3H);13C NMR(100MHz,CDCl3):δ142.8,138.5(d,J=8Hz),137.7(d,J=8Hz),137.2,136.7(d,J=16Hz),135.3(d,J=23Hz),131.7(d,J=18Hz),131.0,130.8(d,J=9Hz),130.3(d,J=12Hz),129.3,128.8(dd,J=6,11Hz),128.1(d,J=8Hz),127.4(d,J=6Hz),126.0,125.5,122.7(d,J=7Hz),121.8,75.3(d,J=14Hz),72.6(d,J=4Hz),71.1,70.1,69.8,61.7,33.4,22.5,20.1;31P NMR(162MHz,CDCl3):δ-39.31(d,J=33.5Hz),-25.49(d,J=35.0Hz).
example 4
Iridium catalyzed asymmetric hydrogenation of imines: a metal precursor [ Ir (COD) Cl]2Stirring the solution and chiral diphosphine ligand in 2L dichloromethane at room temperature for 2h to prepare the chiral iridium catalyst (10)-3mol/L). A200 mL autoclave was replaced three times with nitrogen, the freshly prepared imine 1a was injected, and then the in situ prepared chiral iridium catalyst Ir-L1(S/C ═ 5X 10)5). The reaction mixture was replaced three times with hydrogen, the pressure was adjusted to 60bar and the reaction was carried out at room temperature for 24 hours. After the reaction, the pressure was released, the reaction conversion was greater than 99% by GC analysis, the hydrogenated product 2a was obtained in 99% yield by column chromatography separation, and 93% ee was obtained by HPLC analysis. The detection data of the product of the nuclear magnetic resonance hydrogen spectrum and the high performance liquid chromatography are as follows:1H NMR(400MHz,CDCl3):δ7.20–7.36(m,5H),7.05–7.09(m,2H),6.61–6.65(m,1H),6.48–6.50(m,2H),4.46(q,J=8.0Hz,1H),4.02(br,1H),1.49(d,J=8.0Hz,3H).HPLC(OJ-H,n-hexane/i-PrOH=97/3,1.0mL/min,254nm,40℃):tR(minor)=20.9min,tR(major)=25.5min.
the structural formulas of 1a and 2a are as follows:
example 5
The chiral catalyst Ir-L1 in example 4 was replaced with Ir-L2, and the reaction was performed as in example 4 to obtain a reaction conversion of greater than 99% by GC analysis and 80% ee by HPLC analysis.
Example 6
The chiral catalyst Ir-L1 in example 4 was replaced with Ir-L3, and the reaction was carried out as in example 4 to obtain a reaction conversion of more than 99% by GC analysis and 75% ee by HPLC analysis.
Example 7
The reaction solvent dichloromethane in example 4 was replaced by tetrahydrofuran, and the rest of the example 4 was carried out, giving a reaction conversion of more than 99% by GC analysis and 90% ee by HPLC analysis.
Example 8
The reaction solvent dichloromethane in example 4 was replaced with ethyl acetate as in example 4, and the reaction gave a reaction conversion of greater than 99% by GC analysis and 86% ee by HPLC analysis.
Example 9
Imine 1a in example 4 was replaced with 1b, the remainder being as in example 4, the reaction was complete and 2b was isolated by column chromatography in 99% yield and 92% ee by HPLC. The detection data of the product of the nuclear magnetic resonance hydrogen spectrum and the high performance liquid chromatography are as follows:1H NMR(400MHz,CDCl3):δ7.33(d,J=8.0Hz,2H),7.15(t,J=8.0Hz,2H),6.90(d,J=8.0Hz,2H),6.70(t,J=8.0Hz,1H),6.56(d,J=8.0Hz,2H),4.50(q,J=8.0Hz,1H),4.09(br,1H),3.82(s,3H),1.54(d,J=8.0Hz,3H).HPLC(OD-H,n-hexane/i-PrOH=90/10,1.0mL/min,254nm,40℃):tR(minor)=7.4min,tR(major)=8.1min.
the structural formulas of 1b and 2b are as follows:
example 10
Imine 1a from example 4 was replaced with 1c, the remainder being as in example 4, and the reaction was completed and 2c was isolated by column chromatography in 98% yield and 93% ee by HPLC. The detection data of the product of the nuclear magnetic resonance hydrogen spectrum and the high performance liquid chromatography are as follows:1H NMR(400MHz,CDCl3):δ8.17(d,J=8.0Hz,2H),7.54(d,J=8.0Hz,2H),7.10(t,J=8.0Hz,2H),6.70(t,J=8.0Hz,1H),6.46(d,J=8.0Hz,2H),4.57(q,J=8.0Hz,1H),4.30(br,1H),1.55(d,J=8.0Hz,3H).HPLC(OD-H,n-hexane/i-PrOH=90/10,1.0mL/min,254nm,40℃):tR(minor)=25.7min,tR(major)=27.9min.
the structural formulae of 1c, 2c are as follows:
example 11
Imine 1a from example 4 was replaced with 1d, the remainder being as in example 4, and the reaction was completed and column chromatography gave 2d in 98% yield and 96% ee by HPLC. The detection data of the product of the nuclear magnetic resonance hydrogen spectrum and the high performance liquid chromatography are as follows:1H NMR(400MHz,CDCl3):δ7.31–7.32(m,4H),7.25–7.27(m,1H),6.97(d,J=8.0Hz,2H),6.81(t,J=8.0Hz,1H),4.34(q,J=6.8Hz,1H),3.22(br,1H),2.19(s,6H),1.54(d,J=8.0Hz,3H).HPLC(OJ-H,n-hexane/i-PrOH=90/10,1.0mL/min,254nm,40℃):tR(minor)=4.9min,tR(major)=5.4min.
the structural formulae of 1d, 2d are as follows:
example 12
Imine 1a from example 4 was replaced with 1e, the rest of the same as example 4, reaction was complete, column chromatography gave 2e in 95% yield, and HPLC gave 95% ee. The detection data of the product of the nuclear magnetic resonance hydrogen spectrum and the high performance liquid chromatography are as follows:1H NMR(400MHz,CDCl3):δ7.28–7.35(m,4H),7.19–7.24(m,1H),6.78(t,J=8.0Hz,2H),6.40–6.43(m,2H),4.40(q,J=8.0Hz,1H),3.97(br,1H),1.49(d,J=8.0Hz,3H).HPLC(OD-H,n-hexane/i-PrOH=99/1,1.0mL/min,254nm,40℃):tR(minor)=12.3min,tR(major)=15.5min.
the structural formulae of 1e, 2e are as follows:
example 13
The imine 1a from example 4 was replaced with the s-metolachlor key intermediate 1f (generated from 2-methyl-6-ethylaniline and methoxyacetone), the reaction solvent was dichloroethane, and the hydrogen pressure was 50bar, reaction temperature 80 ℃, the rest of the example 4, 2f obtained after the reaction is finished, yield 95% and 91% ee obtained after HPLC analysis. The detection data of the product of the nuclear magnetic resonance hydrogen spectrum and the high performance liquid chromatography are as follows:1H NMR(400MHz,CDCl3):δ7.02(dd,J=7.6,15.2Hz,2H),6.89(t,J=7.6Hz,1H),3.36-3.40(m,6H),2.67(q,J=7.6Hz,2H),2.31(s,3H),1.25(t,J=7.6Hz,3H),1.20(d,J=5.6Hz,3H).HPLC(OJ-H,n-hexane/i-PrOH=98/2,1.0mL/min,254nm,40℃):tR(minor)=3.9min,tR(major)=4.3min.
the structural formulas of 1f and 2f are as follows:
Claims (9)
1. a method for preparing chiral amine by iridium-catalyzed asymmetric hydrogenation of imine is characterized by comprising the following steps: the method comprises the following steps: imine is taken as a substrate, and asymmetric hydrogenation is carried out on the imine in a reaction solvent under the action of a chiral iridium catalyst under certain hydrogen pressure and temperature to obtain a chiral amine compound.
2. The method for preparing chiral amine by asymmetric hydrogenation of imine catalyzed by iridium as claimed in claim 1, wherein: the method comprises the following specific steps:
(1) preparation of chiral iridium catalyst: under the protection of nitrogen, stirring the iridium-cyclooctadiene complex and chiral diphosphine ligand in a reaction solvent for 2 hours to prepare a chiral iridium catalyst by in-situ coordination;
(2) preparation of chiral amine compound: dissolving substrate imine in a reaction solvent, adding the substrate imine into the stirred chiral iridium catalyst solution, placing the solution in a high-pressure reaction kettle, replacing the solution with hydrogen for 3 times, and then introducing hydrogen; after the reaction, slowly releasing hydrogen, concentrating under reduced pressure until no solvent exists, separating by silica gel column chromatography, concentrating under reduced pressure, and vacuum drying to obtain chiral amine compound.
3. The method for preparing chiral amine by asymmetric hydrogenation of imine catalyzed by iridium as claimed in claim 2, wherein: the imine (1) and the chiral amine compound (2) have the following structures:
in the formula: r1Is C1~C10Alkyl radicals such as CH3、CH3CH2Etc. C3~C12Cycloalkyl radicals such as cyclopentyl, cyclohexyl, etc., or C containing one or more functional groups of N, S, O, P1~C10Alkyl such as methoxymethyl, ethoxymethyl, etc., or C containing one or more functional groups of N, S, O, P3~C10Cycloalkyl groups such as 2-tetrahydrofuryl, 4-tetrahydrofuryl, etc.; or aryl or the like C6-C30Aromatic groups such as phenyl, 4-methoxyphenyl, etc., which may or may not contain N, S, O, P, etc.; or ester groups such as COOCH3、COOCH2CH3Etc.; r2Is H, C1-C40Alkyl or aryl within; ar is C such as phenyl, 2-substituted, 3-substituted, 4-substituted, 2, 6-disubstituted, 2,4, 6-trisubstituted aryl, etc6-C30Aromatic groups containing or not containing N, S, O, P functional groups such as 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 2-methyl-6-ethylphenyl, thiophene, etc.
4. The method for preparing chiral amine by asymmetric hydrogenation of imine catalyzed by iridium as claimed in claim 2, wherein: the iridium-cyclooctadiene complex is [ Ir (COD) Cl]2、Ir(COD)2BARF or Ir (COD)2BF4One kind of (1).
5. The method for preparing chiral amine by asymmetric hydrogenation of imine catalyzed by iridium as claimed in claim 2, wherein: the structural general formula of the chiral diphosphine ligand is as follows:
wherein: r is C1-C40 alkyl and C3-C12 cycloalkyl, phenyl and substituted phenyl, naphthyl and substituted naphthyl, contains one or more than two five-membered or six-membered heterocyclic aromatic groups of oxygen, sulfur and nitrogen atoms, and has 1-5 substituents of C1-C40 alkyl, C1-C40 alkoxy, halogen, nitro, ester group or cyano;
ar is one of phenyl or substituted phenyl, the substituent is one or more of C1-C40 alkyl, C1-C40 alkoxy, halogen, nitro, ester group or cyano, and the number of the substituents is 1-5.
6. The method for preparing chiral amine by asymmetric hydrogenation of imine catalyzed by iridium as claimed in claim 1, wherein:
the solvent is at least one of dichloromethane, 1, 2-dichloroethane or toluene.
7. The method for preparing chiral amine by asymmetric hydrogenation of imine catalyzed by iridium as claimed in claim 2, wherein:
the iridium concentration in the reaction solution is 0.0001-0.01 mol/L;
the molar ratio of the chiral diphosphine ligand to iridium is 1-5: 1;
the molar ratio of the imine substrate to the iridium catalyst is 300000-500000: 1.
8. The method for preparing chiral amine by asymmetric hydrogenation of imine catalyzed by iridium according to claim 1 or 2, wherein: the reaction conditions were controlled as follows:
the hydrogen pressure is 20-100 bar;
the reaction temperature is 20-100 ℃;
the reaction time is 1-24 hours.
9. The method for preparing chiral amine by asymmetric hydrogenation of imine catalyzed by iridium as claimed in claim 1, wherein: the technical route of the invention is as follows:
in the above reaction formula, the general formula (1) represents a reaction substrate imine, and the general formula (2) represents a chiral amine compound.
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Citations (3)
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---|---|---|---|---|
CN108929345A (en) * | 2018-07-18 | 2018-12-04 | 中国人民解放军第四军医大学 | Chiral ferrocene biphosphine ligand and its preparation method and application |
CN109422603A (en) * | 2017-08-29 | 2019-03-05 | 中国科学院大连化学物理研究所 | A kind of method of iridium catalysis asymmetric hydrogenation imines synthesis of chiral amine compounds |
CN110551037A (en) * | 2018-05-31 | 2019-12-10 | 中国科学院大连化学物理研究所 | Method for catalyzing asymmetric hydrogenation of imine by iridium/chiral diphosphine system |
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CN110551037A (en) * | 2018-05-31 | 2019-12-10 | 中国科学院大连化学物理研究所 | Method for catalyzing asymmetric hydrogenation of imine by iridium/chiral diphosphine system |
CN108929345A (en) * | 2018-07-18 | 2018-12-04 | 中国人民解放军第四军医大学 | Chiral ferrocene biphosphine ligand and its preparation method and application |
Non-Patent Citations (3)
Title |
---|
DAO-YONG WANG,ET. AL: "Enantioselective Rh-Catalyzed Hydrogenation of 3-Aryl-2-phosphonomethylpropenoates by a New Class of Chiral Ferrocenyl Diphosphine Ligands", 《ORGANIC LETTERS》 * |
HU, JUAN,ET AL.: "Ir-Catalyzed Enantioselective Hydrogenation of 2H-1,4-Benzoxazines with a Chiral 1,2,3,4-Tetrahydro-1-naphthylamine Derived Phosphine-aminophosphine Ligand", 《CHIN. J. CHEM.》 * |
王东等: "亚胺的不对称催化氢化研究进展", 《有机化学》 * |
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