WO2023040106A1 - 一种绿色的可见光催化的乙酰胺化合物的制备方法 - Google Patents
一种绿色的可见光催化的乙酰胺化合物的制备方法 Download PDFInfo
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- WO2023040106A1 WO2023040106A1 PCT/CN2021/139829 CN2021139829W WO2023040106A1 WO 2023040106 A1 WO2023040106 A1 WO 2023040106A1 CN 2021139829 W CN2021139829 W CN 2021139829W WO 2023040106 A1 WO2023040106 A1 WO 2023040106A1
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- -1 acetamide compound Chemical class 0.000 title claims abstract description 33
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 title claims abstract description 24
- 238000002360 preparation method Methods 0.000 title claims abstract description 16
- 238000006555 catalytic reaction Methods 0.000 title abstract description 5
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 claims abstract description 86
- 238000006243 chemical reaction Methods 0.000 claims abstract description 81
- 239000002994 raw material Substances 0.000 claims abstract description 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 108
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 78
- 150000001412 amines Chemical class 0.000 claims description 46
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 12
- 150000002576 ketones Chemical class 0.000 claims description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 6
- 150000003869 acetamides Chemical class 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- UBOXGVDOUJQMTN-UHFFFAOYSA-N 1,1,2-trichloroethane Chemical compound ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 claims description 4
- BVQVLAIMHVDZEL-UHFFFAOYSA-N 1-phenyl-1,2-propanedione Chemical compound CC(=O)C(=O)C1=CC=CC=C1 BVQVLAIMHVDZEL-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- MWVFCEVNXHTDNF-UHFFFAOYSA-N hexane-2,3-dione Chemical compound CCCC(=O)C(C)=O MWVFCEVNXHTDNF-UHFFFAOYSA-N 0.000 claims description 4
- TZMFJUDUGYTVRY-UHFFFAOYSA-N pentane-2,3-dione Chemical compound CCC(=O)C(C)=O TZMFJUDUGYTVRY-UHFFFAOYSA-N 0.000 claims description 4
- 230000035484 reaction time Effects 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 claims description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims 1
- 239000000758 substrate Substances 0.000 abstract description 14
- 239000003054 catalyst Substances 0.000 abstract description 13
- 238000000034 method Methods 0.000 abstract description 13
- 150000004982 aromatic amines Chemical class 0.000 abstract description 7
- 229910052751 metal Inorganic materials 0.000 abstract description 7
- 239000002184 metal Substances 0.000 abstract description 7
- 239000012024 dehydrating agents Substances 0.000 abstract description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 183
- 238000004458 analytical method Methods 0.000 description 68
- 239000000243 solution Substances 0.000 description 41
- 239000002904 solvent Substances 0.000 description 39
- 238000012360 testing method Methods 0.000 description 37
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 35
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 35
- 238000004440 column chromatography Methods 0.000 description 35
- 239000000741 silica gel Substances 0.000 description 35
- 229910002027 silica gel Inorganic materials 0.000 description 35
- 239000012044 organic layer Substances 0.000 description 34
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical class [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 34
- 238000003756 stirring Methods 0.000 description 34
- 238000006552 photochemical reaction Methods 0.000 description 12
- 125000002252 acyl group Chemical group 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 238000011160 research Methods 0.000 description 4
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 3
- 239000012346 acetyl chloride Substances 0.000 description 3
- 230000021736 acetylation Effects 0.000 description 3
- 238000006640 acetylation reaction Methods 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- NLRKCXQQSUWLCH-UHFFFAOYSA-N nitrosobenzene Chemical compound O=NC1=CC=CC=C1 NLRKCXQQSUWLCH-UHFFFAOYSA-N 0.000 description 3
- IYWJIYWFPADQAN-LNTINUHCSA-N (z)-4-hydroxypent-3-en-2-one;ruthenium Chemical compound [Ru].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O IYWJIYWFPADQAN-LNTINUHCSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000008430 aromatic amides Chemical group 0.000 description 2
- 150000001543 aryl boronic acids Chemical class 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000002360 explosive Substances 0.000 description 2
- GOTYRUGSSMKFNF-UHFFFAOYSA-N lenalidomide Chemical compound C1C=2C(N)=CC=CC=2C(=O)N1C1CCC(=O)NC1=O GOTYRUGSSMKFNF-UHFFFAOYSA-N 0.000 description 2
- 229960004942 lenalidomide Drugs 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 229910052707 ruthenium Inorganic materials 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WHQUHTXULUACFD-KRWDZBQOSA-N (3s)-4-[[2-(4-fluoro-3-methylphenyl)-4-methyl-6-propan-2-ylphenyl]methoxy-hydroxyphosphoryl]-3-hydroxybutanoic acid Chemical compound CC(C)C1=CC(C)=CC(C=2C=C(C)C(F)=CC=2)=C1COP(O)(=O)C[C@@H](O)CC(O)=O WHQUHTXULUACFD-KRWDZBQOSA-N 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
- MLDQJTXFUGDVEO-UHFFFAOYSA-N BAY-43-9006 Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=CC(NC(=O)NC=3C=C(C(Cl)=CC=3)C(F)(F)F)=CC=2)=C1 MLDQJTXFUGDVEO-UHFFFAOYSA-N 0.000 description 1
- 239000005511 L01XE05 - Sorafenib Substances 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 208000034578 Multiple myelomas Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 206010035226 Plasma cell myeloma Diseases 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 238000005910 aminocarbonylation reaction Methods 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 229940041181 antineoplastic drug Drugs 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- UREBDLICKHMUKA-CXSFZGCWSA-N dexamethasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)CO)(O)[C@@]1(C)C[C@@H]2O UREBDLICKHMUKA-CXSFZGCWSA-N 0.000 description 1
- 229960003957 dexamethasone Drugs 0.000 description 1
- 229940000406 drug candidate Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000011134 hematopoietic stem cell transplantation Methods 0.000 description 1
- 206010073071 hepatocellular carcinoma Diseases 0.000 description 1
- 231100000844 hepatocellular carcinoma Toxicity 0.000 description 1
- 208000027866 inflammatory disease Diseases 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000009115 maintenance therapy Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- JKDRQYIYVJVOPF-FDGPNNRMSA-L palladium(ii) acetylacetonate Chemical compound [Pd+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O JKDRQYIYVJVOPF-FDGPNNRMSA-L 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 229960003787 sorafenib Drugs 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- DUYAAUVXQSMXQP-UHFFFAOYSA-M thioacetate Chemical compound CC([S-])=O DUYAAUVXQSMXQP-UHFFFAOYSA-M 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/10—Preparation of carboxylic acid amides from compounds not provided for in groups C07C231/02 - C07C231/08
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B43/00—Formation or introduction of functional groups containing nitrogen
- C07B43/06—Formation or introduction of functional groups containing nitrogen of amide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Definitions
- the invention relates to a preparation method of a green visible light-catalyzed acetamide compound, which belongs to the technical field of organic synthesis.
- the amide bond is a basic functional group that widely exists in nature. According to statistics, about one-quarter of marketed drugs and two-thirds of drug candidates contain amide bonds. The formation of amide bonds is the most widely used organic chemical reaction in synthetic pharmaceutical chemistry. Therefore, it is particularly important to introduce amide bonds into organic molecules.
- the current methods for synthesizing amide compounds have some shortcomings, such as harsh reaction conditions, low yield, narrow substrate range, high reaction temperature, use of relatively expensive metal catalysts, and excessive acid-base additives.
- Olson's research group used pyridine as a base to achieve quantitative acetylation of acetamide and amine under thermal reaction conditions. However, this method requires high temperature and limited substrate range.
- the purpose of the present invention is to provide a green, environmentally friendly, energy-saving and efficient visible light catalytic method to synthesize acetamide compounds.
- the "light" in the photochemical reaction is a special reagent that can participate in the reaction. Metal complexes, organic dyes or semiconductors act as photosensitizers to trigger subsequent reactions.
- the photochemical reaction has the following characteristics: (1) The thermochemical reaction requires a large activation energy, which needs to be heated to a certain temperature for the reaction to occur; while the activation energy required for the photochemical reaction is very small, so at room temperature (2) Complex molecules often contain multiple active groups.
- thermochemical reaction to make one of the groups react, other groups need to be protected; and a photochemical reaction can specifically excite a group according to the position of the group in the molecule to trigger the reaction; (3)
- thermochemical reactions and photochemical reactions are different, so photochemical reactions can be used to synthesize products that cannot be synthesized by thermochemical reactions. Based on these properties of the photochemical reaction, the superiority of the present invention is obvious.
- the light source LED lamp is cheap and easy to obtain, the source of raw materials is abundant, and the reaction substrate has wide applicability (one, two, three, grade aliphatic amines and aromatic amines are all Compatible with this system), mild reaction conditions, no need for any acid-base additives, no catalyst, cheap 2,3-butanedione as the reaction raw material, and the reaction operation is simple.
- the technical solution adopted in the present invention is: a green visible light-catalyzed preparation method of acetamide compounds, which uses amines and ketones as raw materials to prepare acetamide compounds under visible light irradiation.
- R is selected from naphthyl, 7-azaindolyl, alkyl, benzothiazolyl, phenyl and monosubstituted or polysubstituted aryl, wherein the substituents are methyl, isopropyl, tert-butyl, methoxy, tert-butyl, nitro, hydroxyl, cyano, ester, phenyl, fluorine, chlorine, bromine, trifluoromethyl, trifluoromethoxy, acetoxy, amino, acetyl Amino, sulfonamido, etc.; R 2 is selected from hydrogen or alkyl.
- the visible light is LE light
- the LED light is white light, green light or blue light
- the wattage is 18W-60W.
- the LED lamp is a white lamp; the wattage of the white lamp is 40W.
- reaction time is 4 to 12 hours.
- the preferred reaction time is 6 hours.
- the ketone is 2,3-butanedione, 1-phenylpropane-1,2-dione, 2,3-pentanedione, 2,3-hexanedione, and acetone.
- the ketone is 2,3-butanedione.
- the reaction is carried out in an organic solvent;
- the organic solvent is petroleum ether, 1,2-dichloroethane, 1,1,1-trichloroethane, 1,1,2-trichloroethane , nitromethane, acetonitrile, ethyl acetate, acetone, isopropanol or 95% ethanol.
- the amount of ketone used is 5 to 7 times, preferably 6 times, the molar amount of amine.
- the invention adopts cheap aliphatic amine or aromatic amine as reaction substrate, economical and easily available LED lamp as light source, 2,3-butanedione as raw material, and ethanol (95%) solvent.
- the reaction of the present invention is carried out in air. After the reaction, dry with anhydrous sodium sulfate, remove the solvent with a rotary evaporator, adsorb on silica gel, and obtain the acetamide compound through simple column chromatography.
- the 2,3-butanedione used in this paper has a wide range of sources, and the mode of visible light catalysis that is green, mild and environmentally friendly is used to prepare acetamide compound.
- Photochemical reaction is a synthetic method with the goal of cleanliness, energy saving, and saving. Generally, photochemical reaction does not require activation energy, or only requires a small activation energy; at the same time, photochemical reaction can select the corresponding light source according to the absorption wavelength of each group in the molecule.
- the reaction mode is single in the existing technology for synthesizing bisamides ( Most of them are thermal reactions), the reaction substrate is narrow, the reaction yield is low, and excessive acid-base additives and metal catalysts are required.
- the invention has a reaction bottom It has a wide range of substances (one, two, three, grade aliphatic amines and aromatic amines are all compatible with this method), no dehydrating agent is needed, the reaction conditions are simple, the reaction yield is relatively high, and the reaction conditions are mild.
- the technology of the present invention does not need to use expensive and pre-prepared acyl sources, and 2,3-butanedione can directly participate in the reaction, thereby avoiding the problem of overly cumbersome operation.
- the technology of the present invention uses commercially available aromatic amines and aliphatic amine substrates as reaction raw materials. Compared with the prior art, the substrate does not need to be synthesized and is easy to operate. Compared with the prior art, it avoids the use of catalysts. In particular, expensive metals such as iridium, ruthenium, and palladium should be avoided.
- the present invention adopts the strategy of green, environmental protection, gentle, efficient, energy-saving visible light catalysis to synthesize acetamide compound
- the light source is an economical and easy-to-obtain LED lamp
- the reaction substrate amine Both ketones and organic solvents are commercial products and can be purchased directly. 95% ethanol means that the mass percentage of ethanol is 95%, and the rest is water.
- the product acetamide compound can be efficiently obtained only by reacting ketone and amine in an organic solvent under the irradiation of visible light under the condition of no catalyst. The following experiments were carried out in air at room temperature.
- Embodiment one Embodiment one: .
- Embodiment two Embodiment two: .
- Embodiment three Embodiment three: .
- Embodiment four Embodiment four: .
- Embodiment five Embodiment five: .
- Embodiment six Embodiment six: .
- Embodiment seven Embodiment seven: .
- Embodiment eight .
- Embodiment nine .
- Embodiment ten .
- Lenalidomide also known as lenalidomide
- MM myeloma Chemicalbook
- Maintenance therapy in MM after hematopoietic stem cell transplantation And it can also be used in hepatocellular carcinoma. Therefore, late modification of the drug molecule may change its efficacy.
- Compound 3j was derived from this drug molecule.
- Embodiment eleven .
- Embodiment 12 .
- Embodiment thirteen .
- Embodiment 14 .
- Embodiment fifteen .
- Embodiment sixteen .
- Embodiment seventeen .
- Embodiment eighteen .
- Embodiment nineteen .
- Embodiment 20 .
- Embodiment 21 .
- Embodiment 22 .
- Embodiment 23 .
- Embodiment 24 .
- Embodiment 25 .
- Embodiment twenty-six .
- Embodiment 27 .
- Embodiment twenty-eight .
- Embodiment 29 .
- Embodiment Thirty-one .
- Embodiment thirty-two .
- Embodiment thirty-three .
- Embodiment thirty-four .
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Abstract
本发明公开了一种绿色的可见光催化的乙酰胺化合物的制备方法,该方法以LED灯作为光源提供能量,经济易得的芳香胺、脂肪胺以及市场可购买的2,3-丁二酮作为反应底物。与现有技术相比较,本发明方法具有以下优点:1) 采用绿色、高效、节能、环境友好的可见光催化的反应模式;2) 反应体系简单且底物范围广,无需添加金属催化剂和脱水剂;3) 反应产率较高;4) 反应条件温和;5) 操作比较简单;6) 原料廉价易得。
Description
本发明涉及一种绿色的可见光催化的乙酰胺化合物的制备方法,属于有机合成技术领域。
酰胺键是一种广泛存在于自然界的基本官能团。据统计,约四分之一的上市药物与三分之二的候选药物含有酰胺键。酰胺键的形成是药物合成化学中应用最广泛的有机化学反应。因此,将酰胺键引入有机分子中显得尤为重要。通过文献调查发现,目前合成酰胺化合物的方法都存在一些不足之处,诸如反应条件苛刻,产率低、底物范围窄、反应高温、使用比较昂贵的金属催化剂、需要过量的酸碱添加剂等。例如:(1)
1937年,Olson课题组以吡啶作为碱,在热反应条件下实现乙酰胺和胺的定量乙酰化。但是,该方法需要较高的温度,底物范围比较局限。(参见:Olson,
V. R.; Feldman, H. B. Quantitative Acetylation of Amines by Means of Acetyl
Chloride and Pyridine.
J. Am. Chem. Soc.1937, 59, 10, 2003-2005.);(2) 2019年,严国兵课题组以醋酸铜为催化剂,乙腈为溶剂,在80℃条件下实现富电子的苯胺与硫代乙酸盐合成乙酰胺。该方法底物范围非常局限,仅适用于一级富电子芳胺。(参见:Yan,
G.; Huang, D.; Yu, J.; Zhang, J.; Ke, Q.; Tian, F.; Jiang, B.; Ji, C. A.;
Zhang, L. Copper-Catalyzed Acetylation of Electron-Rich Phenols and Anilines.
Synlett2019,
30, 06, 726-730.);(3) 2019年,Asachenko等人报道了苯酯胺解法来合成酰胺。该方法需要采用易制爆的氢化钠为碱;反应需要130℃的高温;底物比较局限,仅能合成二级芳酰胺;反应时间较长;反应条件比较危险。(参见:zhevskiy, S. A.;
Ageshina, A. A.; Chesnokov, G. A.; Gribanov, P. S.; Topchiy, M. A.; Nechaev, M.
S.; Asachenko, A. F. Solvent- and transition metal-free amide synthesis from
phenyl esters and aryl amines.
RSC Advances. 2019,
9, 3,
1536-1540.);(4)2019年,吴晓峰课题组利用乙酰丙酮钯为催化剂,六羰基钼为酰基源,过量的碳酸钾为碱,在110℃的高温下实现了由芳基硼酸和硝基苯制备二级芳香族酰胺。该体系新颖,但是操作复杂,不仅需要昂贵的催化剂和酰基源,还需要加入复杂的配体结构,很难在工业上有所应用。(参见:Peng,
J. B.; Li, D.; Geng, H. Q.; Wu, X. F. Palladium-Catalyzed Amide Synthesis via
Aminocarbonylation of Arylboronic Acids with Nitroarenes.
Org. Lett.
2019,
21, 12, 4878-4881.);(5)2007年,Adapa课题组,三(乙酰丙酮酸)钌为催化剂,乙酰氯为酰基源,成功制备乙酸酯类化合物。该方法虽然产率较高,但是使用了比较昂贵的金属催化剂,并且由于乙酰氯易水解,将不利于工业上的大规模合成应用。(参见:Varala,
R.; Nasreen, A.; Adapa, S. R., Ruthenium(III) acetylacetonate [Ru(acac)
3]
— An efficient recyclable catalyst for
the acetylation of phenols, alcohols, and amines under neat conditions.
Can.
J. Chem.
2007,
85, 148-152.);(6)2021年,姚秋丽课题组,以亚硝基苯为原料,过量的氯化钠为添加剂,2,3-丁二酮为乙酰基源,实现一级芳香族乙酰胺的制备。该方法采用了价格较昂贵的且易制爆、毒性大的亚硝基苯为原料。并且原料需要预制备,传统的亚硝基苯由苯胺氧化制备获得。除此之外,该方法底物普适性差,仅适用于一级芳胺。(参见:Ran,
M.; He, J.; Yan, B.; Liu, W.; Li, Y.; Fu, Y.; Li, C. J.; Yao, Q., Catalyst-free
generation of acyl radicals induced by visible light in water to construct C-N
bonds.
Org. Biomol. Chem.2021,
19, 1970-1975.)。
综上所述,目前报道的这些酰胺化合物的合成方法,反应过程比较繁琐,采用过量的碱、昂贵的金属催化剂以及酰基源、反应条件比较苛刻、反应模式比较单一(绝大多数为热反应)。因此,发展一种原料来源丰富、底物范围广、绿色、温和、高效、节能、环境友好的可见光催化的乙酰胺化方法显得尤为重要。
本发明的目的是提供一种绿色、环境友好、节能高效的可见光催化的方法来合成乙酰胺化合物,光化反应中的“光”是一种特殊的、能够参与反应的试剂,利用具有可见光吸收的金属配合物、有机染料或半导体作为光敏剂,引发后续的反应。与经典的热化学反应相比,光化学反应具有以下特点:(1)热化学反应需要较大的活化能,需要加热到一定温度反应才能发生;而光化学反应所需活化能很小,因此在室温下可以快速进行;(2)复杂的分子往往含有多个活性基团。热化学反应中要使其中某一个基团发生反应,需要将其它基团保护起来;而光化学反应可以根据基团在分子中的部位不同特定激发某一基团来引发反应的发生;(3)多数情况下热化学反应与光化学反应的产物不同,因此可利用光化学反应合成热化学反应不能合成的产物。基于光化学反应的这些性质,本发明的优越性显而易见,该反应体系中光源LED灯廉价易得、原料来源丰富、反应底物普适性广(一、二、三、级脂肪胺和芳香胺均兼容于该体系)、反应条件温和、无需任何酸碱添加剂、无催化剂、廉价的2,3-丁二酮作为反应原料,反应操作简便。
为达到上述发明目的,本发明采用的技术方案是:一种绿色的可见光催化的乙酰胺化合物的制备方法,在可见光照射下,以胺、酮为原料,反应制备乙酰胺化合物。
上述化学结构式中,R
1选自萘基、7-氮杂吲哚基、烷基、苯并噻唑基、苯基以及单取代或多取代芳基,其中取代基为甲基、异丙基、叔丁基、甲氧基、叔丁基、硝基、羟基、氰基、酯基、苯基、氟、氯、溴、三氟甲基、三氟甲氧基、乙酰氧基、氨基、乙酰氨基、磺酰胺基等;R
2选自氢或者烷基。
上述技术方案中,所述可见光为LE灯光,LED灯为白灯、绿灯或者蓝灯;瓦数为18W~60W。优选的技术方案中,所述的LED灯为白灯;白灯的瓦数为40W。
上述技术方案中,反应的时间为4~12小时。优选的反应时间为6小时。
上述技术方案中,所述酮为2,3-丁二酮、1-苯基丙烷-1,2-二酮、2,3-戊二酮、2,3-己二酮、丙酮。优选的技术方案中,酮为2,3-丁二酮。
上述技术方案中,反应在有机溶剂中进行;所述有机溶剂为石油醚、1,2-二氯乙烷、1,1,1-三氯乙烷、1,1,2-三氯乙烷、硝基甲烷、乙腈、乙酸乙酯、丙酮、异丙醇或者95%乙醇。
上述技术方案中,酮的用量为胺摩尔量的5~7倍,优选6倍。
本发明采用廉价的脂肪胺或芳香胺为反应底物、经济易得的LED灯为光源、2,3-丁二酮作为原料、乙醇(95%)溶剂。本发明的反应在空气中进行。反应结束后,用无水硫酸钠干燥,用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得乙酰胺化合物。
由于上述技术方案的运用,本发明与现有技术相比具有下列优点:1.本文所使用的2,3-丁二酮来源广泛,采用绿色、温和、环境友好的可见光催化的模式制备乙酰胺化合物。光化学反应是以洁净、节能、节约为目标的合成方法,光化学反应一般不需要活化能,或者只需要很小的活化能;同时光化学反应可以根据分子中各个基团吸收波长的不同选择对应的光源,选择性地激发某一基团引发反应的发生;巧妙利用光化学反应往往可以大幅度缩短目标产物的合成路线,基于光化学反应的性质,与现有的合成双胺化物的技术中反应模式单一(大多数为热反应),反应底物窄,反应产率低,需要过量的酸碱添加剂和金属催化剂、反应条件苛刻相比(需要高温,强还原剂,高能耗等),该发明具有反应底物范围广(一、二、三、级脂肪胺和芳香胺均兼容于该方法),无需脱水剂,反应条件简单,反应产率比较高,反应条件温和等特点。
2.本发明的技术不需要采用昂贵、预制备的酰基源,2,3-丁二酮可以直接参与反应,从而避免了操作上过于繁琐的问题。
3.本发明技术使用商业上可购买的芳香胺和脂肪胺底物作为反应原料,与现有的技术相比,底物无需合成,操作简便,与现有的技术相比,避免使用催化剂,尤其避免使用昂贵的铱、钌、钯等价格昂贵的金属。
下面结合实例对本发明作进一步描述:本发明采用了绿色、环保、温和、高效、节能的可见光催化的策略来合成乙酰胺化合物,在该发明中光源为经济易得的LED灯,反应底物胺与酮、有机溶剂皆商业化产品,可以直接购买获得,95%乙醇是指乙醇的质量百分数为95%,其余为水。本发明在无催化剂条件下,仅以酮、胺在有机溶剂中,可见光照射下反应,即可高效得到产物乙酰胺化合物。以下实验在空气中、室温下进行。
在25 mL Schlenk试管中依次加入胺1a
(0.2 mmol,34.2mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3a,收率为85%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.05 (s, 1H),
7.56 – 7.44 (m, 4H), 2.04 (s, 3H).
13C
NMR (100 MHz, DMSO) δ 168.4, 138.7,
131.4, 120.8, 114.5, 24.0. HRMS (ESI-TOF): Anal Calcd. For. C
8H
8
79BrNO+H
+:213.9862, Found: 213.9860; C
8H
8
81BrNO+H
+:
215.9842, Found: 215.9840. IR (neat, cm
-1): υ 3376, 2851, 1649, 1538, 1491, 1396, 1258, 1046, 991,
825, 763。
a反应条件: 空气氛围, 1a (0.2 mmol),2a (6.0 equiv.) ,溶剂 (0.5
mL) ,40 W 白色 LEDs
照射6h。
在25 mL Schlenk试管中依次加入胺1b
(0.2 mmol,24.6 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3b,收率为69%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.76 (s, 1H),
7.48 – 7.46 (m, 2H), 6.86 – 6.84 (m, 2H), 3.70 (s, 3H), 2.00 (s, 3H).
13C
NMR (100 MHz, DMSO) δ 167.7, 155.0,
132.5, 120.5, 113.8, 55.1, 23.8. HRMS (ESI-TOF): C
9H
11NO
2+H
+:
166.0863, Found: 166.0862. IR (neat, cm
-1): υ 3365, 1645, 1553, 1512, 1246, 1024, 990, 826, 763。
在25 mL Schlenk试管中依次加入胺1c
(0.2 mmol,22.2 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3c,收率为83%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.97 (s, 1H),
7.60 – 7.56 (m, 2H), 7.14-7.09 (m, 2H), 2.03
(s, 3H).
13C NMR (100 MHz, DMSO) δ
168.1, 157.8 (d,
J = 237.0 Hz), 135.7 (d,
J = 3.0 Hz), 120.7 (d,
J
= 7.0 Hz), 115.2 (d,
J = 22 Hz), 23.9.
19F NMR (377 MHz,
DMSO) δ -119.8 (s, 1F). HRMS (ESI-TOF): Anal
Calcd. For. C
8H
8FNO+H
+: 154.0663, Found:
154.0661. IR (neat, cm
-1): υ 3360, 1645, 1509, 1406, 1377, 1213, 1024, 989, 826。
在25 mL Schlenk试管中依次加入胺1d
(0.2 mmol,35.4 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3d,收率为90%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.14 (s, 1H),
7.69 – 7.67 (m, 2H), 7.28 – 7.25 (m, 2H), 2.05 (s, 3H).
13C NMR (100 MHz,
DMSO) δ 168.5, 143.3, 138.5, 121.5, 120.2,
23.9.
19F NMR (377 MHz, DMSO) δ
-57.1 (s, 1F). HRMS (ESI-TOF): Anal Calcd. For. C
9H
8F
3NO
2+H
+:
220.0580, Found: 220.0578. IR (neat, cm
-1): υ 3378, 3270, 1665, 1618, 1556, 1508, 1154, 992, 825, 762,
659。
在25 mL Schlenk试管中依次加入胺1e
(0.2 mmol,25.4 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇 (95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3e,收率为86%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.05 (s, 1H),
7.61 – 7.59 (m, 2H), 7.34 – 7.32 (m, 2H), 2.04 (s, 3H).
13C NMR (100 MHz,
DMSO) δ 168.4, 138.3, 128.5, 126.5, 120.5,
24.0. HRMS (ESI-TOF): Anal Calcd. For. C
8H
8
35ClNO+H
+:
170.0367, Found: 170.0366; C
8H
8
37ClNO+H
+:
172.0338, Found: 172.0340. IR (neat, cm
-1): υ 3393, 2920, 1658, 1547, 1487, 1392, 1258, 1092, 996,
821, 709。
在25 mL Schlenk试管中依次加入胺1f
(0.2 mmol,27.0 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3f,收率为94%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.50 (s, 1H),
7.16 – 7.14 (m, 2H), 6.83 – 6.81 (m, 2H), 2.19 – 2.18
(m, 1H), 1.70 (s, 3H), 0.85 (d,
J = 6.9 Hz, 6H).
13C NMR (100
MHz, DMSO) δ 168.0, 143.0, 137.1, 126.3, 119.1,
32.8, 23.9, 23.9. HRMS (ESI-TOF): Anal Calcd. For. C
11H
15NO+H
+:
178.1226, Found:178.1225. IR (neat, cm
-1): υ 3285, 2958, 1661, 1542, 1460, 1320, 1264, 1023, 835,
764, 608。
在25 mL Schlenk试管中依次加入胺1g
(0.2 mmol, 43.8 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3g,收率为77%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.01 (s, 1H),
7.62 – 7.60 (m, 2H), 7.43 – 7.40 (m, 2H), 2.03 (s, 3H).
13C NMR (100 MHz,
DMSO) δ 168.5, 139.1, 137.3, 121.2, 86.3, 24.0.
HRMS (ESI-TOF): Anal Calcd. For. C
8H
8INO+ H
+:
261.9723, Found: 261.9721. IR (neat, cm
-1): υ 3392, 2958, 2849, 1663, 1596, 1579, 1482, 1253, 1024,
992, 814, 731, 679。
在25 mL Schlenk试管中依次加入胺1h (0.2
mmol, 48.6 mg)、2,3-丁二酮 (1.2
mmol, 103.3 mg)、乙醇 (95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3h,收率为64%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。化合物1h为抗癌药索拉非尼中间体,对其进行修饰将有利于这类药物分子的进一步应用。
1H NMR
(400 MHz, DMSO) δ 10.10 (s, 1H),
8.79 – 8.76 (m, 1H), 8.50-8.49 (m, 1H), 7.70 – 7.69 (m, 2H), 7.36 (d,
J = 0.6 Hz 1H), 7.17 – 7.15 (m, 2H), 7.14 – 7.12
(m, 1H), 2.78 (d,
J = 4.9 Hz, 3H), 2.06 (s, 3H).
13C NMR (100
MHz, DMSO) δ 168.8, 166.3, 164.2, 152.9, 150.8,
148.5, 137.6, 121.8, 121.2, 114.5, 109.1, 100.0, 26.5, 24.4. HRMS (ESI-TOF):
Anal Calcd. For. C
15H
15N
3O
3+H
+:
286.1186, Found: 286.1184. IR (neat, cm
-1): υ 3354, 2921, 1672, 1538, 1454, 1369, 1254, 1065, 894,
758, 685。
在25 mL Schlenk试管中依次加入胺1i
(0.2 mmol, 30.6 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3i,收率为80%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 8.98 (s, 1H),
7.64 (d,
J = 8.7 Hz, 1H), 6.59 (d,
J = 2.6 Hz, 1H), 6.46 (dd,
J
= 8.7, 2.6 Hz, 1H), 3.79 (s, 3H), 3.73 (s, 3H), 2.02 (s, 3H).
13C
NMR (100 MHz, DMSO) δ 168.2, 156.7,
151.5, 123.9, 120.5, 104.0, 98.7, 55.6, 55.3, 23.5. HRMS (ESI-TOF): Anal Calcd.
For. C
10H
13NO
3+H
+: 196.0968, Found:
196.0968. IR (neat, cm
-1): υ
3421, 1731, 1670, 1528, 1455, 137, 1247, 1049, 822, 760。
在25 mL Schlenk试管中依次加入胺1j
(0.2 mmol, 51.8 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3j,收率为50%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。来那度胺(又称雷利度胺)已被成功地用于治疗炎症性疾病和癌症,其中FDA批准适应症为:合并地塞米松治疗多发性骨髓瘤Chemicalbook(MM);作为接受过自体造血干细胞移植的MM后的维持治疗。并且它也可以用在肝细胞肝癌上。因此,对该药物分子的后期修饰将可能改变其药效。化合物3j衍生于该药物分子。
1H NMR
(400 MHz, DMSO) δ 11.02 (s, 1H),
9.83 (s, 1H), 7.83-7.81 (m, 1H), 7.52 – 7.47
(m, 2H), 5.15 (dd,
J = 13.3, 5.1 Hz, 1H), 4.43 – 4.31 (q,
J = 17.5 Hz, 2H), 2.97 – 2.88 (m, 1H), 2.63 – 2.59
(m, 1H), 2.40 – 2.29 (m, 1H), 2.09 (s, 3H), 2.05 – 1.99 (m, 1H).
13C NMR (100 MHz, DMSO) δ 172.9, 171.1, 168.5, 167.9, 133.8, 133.7, 132.7, 128.7,
125.20, 119.1, 51.6, 46.5, 31.3, 23.5, 22.7. HRMS (ESI-TOF): Anal Calcd. For. C
15H
15N
3O
4+Na
+:
324.0955, Found: 324.0953. IR (neat, cm
-1): υ 3379, 2960, 1662, 1545, 1462, 1322, 1267, 1046, 991,
826, 763。
在25 mL Schlenk试管中依次加入胺1k
(0.2 mmol, 25.8 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3k,收率为97%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.29 (s, 1H),
7.31 – 7.26 (m, 2H), 6.87 – 6.81 (m, 1H), 2.06 (s, 3H).
13C NMR (100 MHz,
DMSO) δ 169.0, 162.44 (dd,
J = 242.8,
15.3 Hz), 141.77 (t,
J = 14.0 Hz), 101.69 (d,
J = 29.2 Hz), 98.03
(t,
J = 26.2 Hz), 24.07.
19F NMR (377 MHz, DMSO) δ -109.5 (s, 2F). HRMS (ESI-TOF): Anal Calcd. For. C
8H
7F
2NO+H
+:
172.0568, Found: 172.0568. IR (neat, cm
-1): υ 3450, 1700, 1653, 1500, 1051, 655。
在25 mL Schlenk试管中依次加入胺1l
(0.2 mmol, 37.2 mg)、2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3l,收率为74%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.98 (s, 1H),
9.72 (s, 1H), 7.50 – 7.49 (m, 1H),
7.35 – 7.32 (m, 1H), 7.24 – 7.20 (m, 1H), 6.87 – 6.85
(m, 1H), 2.96 (s, 3H), 2.02 (s, 3H).
13C NMR (100 MHz, DMSO) δ 168.4, 140.1, 138.7, 129.4, 114.5, 110.3, 54.9, 24.0.
HRMS (ESI-TOF): Anal Calcd. For. C
9H
12N
2O
3S+H
+:
229.0641, Found: 229.0640. IR (neat, cm
-1): υ 3398, 3274, 2240, 1674, 1608, 1542, 1471, 1301, 1200,
1053, 904, 820, 724, 648。
在25 mL Schlenk试管中依次加入胺1m
(0.2 mmol, 46.4 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3m,收率为57%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, CDCl
3) δ 8.44 (s, 1H),
7.66 (s, 1H), 7.54 (d,
J = 3.5 Hz, 1H), 7.44 (d,
J = 8.4 Hz, 1H),
7.30 (s, 1H), 6.50 (d,
J = 3.5 Hz, 1H), 2.18 (s, 3H), 1.67 (s, 9H).
13C
NMR (100 MHz, CDCl
3) δ
168.5, 149.7, 135.2, 134.7, 127.2, 125.9, 120.9, 115.8, 107.3, 107.0, 83.9,
28.1, 24.5. HRMS (ESI-TOF): Anal Calcd. For. C
15H
18N
2O
3+H
+:
275.1390, Found: 275.1388. IR (neat, cm
-1): υ 3300, 2933, 1731,1662, 1524, 1433, 1214, 1024, 906, 726,
647。
在25 mL Schlenk试管中依次加入胺1n
(0.2 mmol, 30.2 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3n,收率为60%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.54 (s, 1H),
8.22 – 8.20 (m, 1H), 7.90 – 7.88 (m, 1H), 7.61 – 7.56
(m, 1H), 7.20 – 7.15 (m, 1H), 3.85 (s, 3H), 2.11 (s,
3H).
13C NMR (100 MHz, DMSO) δ
168.5, 167.5, 139.6, 133.9, 130.4, 123.1, 121.2, 117.8, 52.4, 24.6. HRMS
(ESI-TOF): Anal Calcd. For. C
10H
11NO
3+H
+:
194.0812, Found: 194.0812. IR (neat, cm
-1): υ 3385, 2955, 1684, 1588, 1524, 1368, 1296, 993, 824, 760。
在25 mL Schlenk试管中依次加入胺1o
(0.2 mmol, 23.6 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3o,收率为73%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.36 (s, 1H),
7.75 (s, 4H), 2.09 (s, 3H).
13C NMR (100 MHz, DMSO) δ 169.2, 143.5, 133.2, 119.1, 118.9, 104.7, 24.2. HRMS
(ESI-TOF): Anal Calcd. For. C
9H
8N
2O+H
+:
161.0709, Found: 161.0710. IR (neat, cm
-1): υ 3301, 3257, 2924, 2221, 1666, 1596, 1403, 1319, 1203,
1024, 996, 818, 714, 648。
在25 mL Schlenk试管中依次加入胺1p
(0.2 mmol, 23.6 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3p,收率为63%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.17 (s, 1H),
9.35 (s, 1H), 8.47 (d,
J = 1.9 Hz, 1H), 8.03 (d,
J = 8.7 Hz, 1H),
7.58 (dd,
J = 8.7, 1.9 Hz, 1H), 2.09 (s, 3H).
13C NMR (100
MHz, DMSO) δ 168.6, 156.8, 153.6, 138.0, 127.7,
122.3, 117.9, 112.6, 24.1. HRMS (ESI-TOF): Anal Calcd. For. C
9H
8N
2OS+H
+:
193.0430, Found: 193.0430. IR (neat, cm
-1): υ 3414, 1731, 1665, 1526, 1444, 1374, 1247, 1023, 823, 760。
在25 mL Schlenk试管中依次加入胺1q
(0.2 mmol, 26.6 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3q,收率为55%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 11.51 (s, 1H),
9.93 (s, 1H), 8.25 (d,
J = 2.3 Hz, 1H), 8.22 (d,
J = 2.3 Hz, 1H),
7.43 – 7.31 (m, 1H), 6.40 (dd,
J = 3.4,
1.9 Hz, 1H), 2.06 (s, 3H).
13C NMR (100 MHz, DMSO) δ 168.3, 145.3, 136.0, 1128.9, 126.8, 119.1, 119., 99.8,
23.7. HRMS (ESI-TOF): Anal Calcd. For. C
9H
9N
3O+H
+:
176.0818, Found: 176.0817. IR (neat, cm
-1): υ 3415, 2922, 1620, 1548, 1210, 1005, 745。
在25 mL Schlenk试管中依次加入胺1r
(0.2 mmol, 18.6 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3r,收率为93%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.93 (s, 1H),
7.58 – 7.56 (m, 2H), 7.30 – 7.26 (m, 2H), 7.01 (t,
J = 7.4 Hz, 3H), 2.03 (s,
3H).
13C NMR (100 MHz, DMSO) δ
168.4, 139.4, 128.7, 123.0, 119.0, 24.1. HRMS (ESI-TOF): Anal Calcd. For. C
8H
9NO
+H
+: 136.0757, Found: 136.0757. IR (neat, cm
-1): υ 3587, 2900, 1732, 1683, 1598, 1496, 1373, 1023, 822,
759, 696。
在25 mL Schlenk试管中依次加入胺1s
(0.2 mmol, 21.4 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3s,收率为93%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.84 (s, 1H),
7.45 (d,
J = 8.4 Hz, 2H), 7.07 (d,
J = 8.4 Hz, 2H), 2.23 (s, 3H),
2.01 (s, 3H).
13C NMR (100 MHz, DMSO) δ
168.1, 136.9, 131.9, 129.1, 119.1, 24.0, 20.5. HRMS (ESI-TOF): Anal Calcd. For.
C
9H
11NO
2+H
+: 166.0863, Found:
166.0862. IR (neat, cm-1): υ 3298, 2976,
1662, 1590, 1488, 922, 816,729。
在25 mL Schlenk试管中依次加入胺1t
(0.2 mmol, 29.8 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3t,收率为71%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.85 (s, 1H),
7.48 (d,
J = 8.7 Hz, 2H), 7.28 (d,
J = 8.7 Hz, 2H), 2.01 (s, 3H),
1.24 (s, 9H).
13C NMR (100 MHz, DMSO) δ
168.1, 145.3, 136.8, 125.3, 118.8, 34.0, 31.2, 24.0. HRMS (ESI-TOF): Anal
Calcd. For. C
12H
17NO+H
+: 192.1383, Found: 192.1382.
IR (neat, cm
-1): υ 3396, 3253,
2949, 1689, 1543, 1495, 1375, 1267, 1022, 998, 834, 760。
在25 mL Schlenk试管中依次加入胺1u
(0.2 mmol, 28.6 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3u,收率为90%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.15 (s, 1H),
8.28 (d,
J = 2.0 Hz, 1H), 7.81 (dd,
J = 17.7, 8.8 Hz, 3H), 7.56
(dd,
J = 8.8, 2.0 Hz, 1H), 7.47 – 7.43
(m, 1H), 7.40 – 7.36 (m, 1H), 2.10 (s, 3H).
13C
NMR (100 MHz, DMSO) δ 168.7, 136.9,
133.5, 129.7, 128.3, 127.5, 127.3, 126.4, 124.5, 119.9, 114.9, 24.2. HRMS
(ESI-TOF): Anal Calcd. For. C
12H
11NO+H
+:
186.0913, Found: 186.0913. IR (neat, cm
-1): υ 3405, 3293, 1670, 1527, 1489, 1393, 1258, 1049, 823, 760。
在25 mL Schlenk试管中依次加入胺1v
(0.2 mmol, 30.0 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3v,收率为66%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.92 (s, 2H),
7.87 (s, 1H), 7.26 – 7.24 (m, 2H),
7.16 (dd,
J = 8.7, 7.2 Hz, 0H), 2.02 (s, 3H).
13C NMR (100
MHz, DMSO) δ 168.4, 139.6, 128.8, 113.9, 109.8,
24.1. HRMS (ESI-TOF): Anal Calcd. For. C
10H
12N
2O
2+H
+:
193.0972, Found: 193.0971. IR (neat, cm
-1): υ 3404, 1665, 1550, 1485, 1419, 1373, 1049, 823, 761。
在25 mL Schlenk试管中依次加入胺1w
(0.2 mmol, 30.0 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3w,收率为67%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.06 (s, 1H),
7.70 (d,
J = 8.7 Hz, 2H), 7.64 – 7.60
(m, 4H), 7.43 (t,
J = 7.7 Hz, 2H), 7.31 (t,
J = 7.7 Hz, 1H), 2.08
(s, 1H).
13C NMR (100 MHz, DMSO) δ
168.4, 139.8, 138.9, 134.7, 128.9, 127.0, 126.9, 126.2, 119.4, 24.1. HRMS
(ESI-TOF): Anal Calcd. For. C
14H
13NO+H
+:
212.1070, Found: 212.1069. IR (neat, cm
-1): υ 3354, 2963, 1672, 1600, 1538, 1452, 1199, 1007, 895,
758, 685。
在25 mL Schlenk试管中依次加入胺1x
(0.2 mmol, 30.0 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、异丙醇 (0.5
mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3x,收率为64%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.47 (s, 1H),
7.18 (d,
J = 8.7 Hz, 2H), 6.48 (d,
J = 8.7 Hz, 2H), 4.81 (s, 2H),
1.95 (s, 3H).
13C NMR (100 MHz, DMSO) δ
167.3, 144.6, 128.6, 120.9, 113.8, 23.7. HRMS (ESI-TOF): Anal Calcd. For. C
8H
10N
2O+H
+:
151.0866, Found: 151.0865. IR (neat, cm
-1): υ 3357, 3305, 1641, 1553, 1429, 1264, 1024, 989, 826。
在25 mL Schlenk试管中依次加入胺1y
(0.2 mmol, 30.0 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3y,收率为53%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.79 (s, 1H),
9.34 (s, 1H), 7.20 (t,
J = 2.0 Hz, 1H), 7.04 (t,
J = 8.1 Hz, 1H),
6.92 (d,
J = 8.1 Hz, 1H), 6.44 – 6.42
(m, 1H), 2.01 (s, 3H).
13C NMR (100 MHz, DMSO) δ 168.3, 157.6, 140.4, 129.4, 110.2, 109.8, 106.3, 24.1.
HRMS (ESI-TOF): Anal Calcd. For. C
8H
9NO
2+H
+:
152.0706, Found: 152.0706. IR (neat, cm
-1): υ 3299, 3261, 2926, 1661, 1513, 1453, 1371, 908, 816, 729,
647。
在25 mL Schlenk试管中依次加入胺1z
(0.2 mmol, 30.0 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3z,收率为64%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 9.46 (s, 1H),
7.67 – 7.58 (m, 2H), 7.27 – 7.33 (m, 1H), 7.13 – 7.09
(m, 1H), 2.07 (s, 3H).
13C NMR (100 MHz, DMSO) δ 168.5, 136.4, 132.6, 127.9, 127.3, 126.9, 117.9, 23.3.
HRMS (ESI-TOF): Anal Calcd. For. C
8H
8
79BrNO+H
+:
213.9862, Found: 213.9861; C
8H
8
81BrNO+H
+:
215.9842, Found: 215.9841. IR (neat, cm
-1): υ 3410, 1660, 1510, 1430, 1207, 1005, 785, 690。
在25 mL Schlenk试管中依次加入胺1aa
(0.2 mmol, 30.4 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3aa,收率为78%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 10.28 (s, 1H),
8.34 (d,
J = 2.2 Hz, 1H), 7.66 (dd,
J = 8.4, 2.2 Hz, 1H), 7.36
(d,
J = 8.4 Hz, 1H), 2.42 (s, 3H), 2.06 (s, 3H).
13C NMR (100
MHz, DMSO) δ 168.9, 148.5, 138.2, 133.0, 126.9,
123.5, 114.1, 24.0, 19.2. HRMS (ESI-TOF): Anal Calcd. For. C
9H
10N
2O
3+H
+:
195.0764, Found: 195.0764. IR (neat, cm
-1): υ 3353, 1672, 1537, 1489, 1392, 1198, 990, 894, 758, 684。
在25 mL Schlenk试管中依次加入胺1ab
(0.2 mmol, 29.2 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3ab,收率为45%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, CDCl
3) δ 7.47 (t,
J
= 7.5 Hz, 2H), 7.40 (t,
J = 7.5 Hz, 1H), 7.27 – 7.24 (m, 2H), 3.96 (t,
J = 6.8 Hz, 2H), 2.70 (t,
J
= 6.8 Hz, 2H), 1.88 (s, 3H).
13C NMR (100 MHz, CDCl
3) δ 170.9, 142.1, 130.0, 128.5, 127.8, 117.8, 45.2, 22.5,
16.4. HRMS (ESI-TOF): Anal Calcd. For. C
11H
12N
2O+H
+:
189.1022, Found: 189.1020. IR (neat, cm
-1): υ 2934, 2251, 1655, 1596, 1494, 1395, 1202, 1025, 908,
726, 646。
在25 mL Schlenk试管中依次加入胺1ac
(0.2 mmol, 31.4 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3ac,收率为52%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 8.06 – 8.03 (m, 1H), 8.00 – 7.98
(m, 1H), 7.75 – 7.73 (m, 1H), 7.66-7.52 (m, 4H), 3.22
(s, 3H), 1.61 (s, 3H).
13C NMR (100 MHz, DMSO) δ 169.6, 140.4, 134.3, 129.5, 128.4, 127.6, 126.7, 126.2,
125.8, 121.9, 36.5, 21.6. HRMS (ESI-TOF): Anal Calcd. For. C
13H
13NO+H
+:
200.1070, Found: 200.1067. IR (neat, cm
-1): υ 1652, 1541, 1488, 1379, 823, 761, 626。
在25 mL Schlenk试管中依次加入胺1ad
(0.2 mmol, 27.4 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3ad,收率为63%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 7.46 – 7.42 (m, 2H), 7.37 – 7.32
(m, 3H), 4.67 (s, 1H), 3.65 (t,
J = 6.5 Hz, 2H), 3.43 (dd,
J =
11.9, 6.5 Hz, 2H), 1.71 (s, 3H).
13C NMR (100 MHz, DMSO) δ 169.1, 143.4, 129.5, 128.2, 127.6, 57.9, 50.9, 22.6.
HRMS (ESI-TOF): Anal Calcd. For. C
10H
13NO
2+H
+:
180.1019, Found: 180.1016. IR (neat, cm
-1): υ 3384, 3063, 2927, 2878, 1716, 1630, 1593, 1494, 1397,
1279, 996, 852, 733。
在25 mL Schlenk试管中依次加入胺1ae
(0.2 mmol, 29.8 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3ae,收率为70%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, CDCl
3) δ 7.44 – 7.40 (m, 2H), 7.36 – 7.33
(m, 1H), 7.17 – 7.15 (m, 1H), 3.71 – 3.67 (m, 2H), 1.82 (s, 3H), 1.52 – 1.44 (m, 2H), 1.29 – 1.26
(m, 2H), 0.88 (t,
J = 7.3 Hz, 2H).
13C NMR (100 MHz, DMSO) δ 168.6, 142.8, 129.5, 128.0, 127.5, 47.6, 29.4, 22.5,
19.4, 13.6. HRMS (ESI-TOF): Anal Calcd. For. C
12H
17NO+H
+:
192.1383, Found: 192.1380. IR (neat, cm
-1): υ 2956, 1649, 1516, 1455, 1383, 1261, 1083, 908, 826, 732。
在25 mL Schlenk试管中依次加入胺1af
(0.2 mmol, 24.2 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3af,收率为73%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, DMSO) δ 7.47 – 7.44 (m, 2H), 7.38 – 7.35
(m, 1H), 7.29 – 7.27 (m, 1H), 3.63 (q,
J = 7.1
Hz, 2H), 1.70 (s, 3H), 0.98 (t,
J = 7.1 Hz, 3H).
13C NMR (100
MHz, DMSO) δ 168.4, 142.61, 129.6, 128.2, 127.6,
43.0, 22.5, 12.9. HRMS (ESI-TOF): Anal Calcd. For. C
10H
13NO+H
+:
164.1070, Found: 164.1068. IR (neat, cm
-1): υ 3368, 2932, 1640, 1594, 1496, 1300, 1259, 1046, 990,
826, 765。
在25 mL Schlenk试管中依次加入胺1af
(0.2 mmol, 36.6 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3af,收率为69%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, CDCl
3) δ 7.34 – 7.18 (m, 8H), 6.99 – 6.97
(m, 2H), 4.89 (s, 2H), 1.88 (s, 3H).
13C NMR (100 MHz, CDCl
3)
δ 170.3, 142.8, 137.4, 129.5, 128.7,
128.3, 128.2, 127.8, 127.3, 52.7, 22.7. HRMS (ESI-TOF): Anal Calcd. For. C
15H
15NO+H
+:
226.1226, Found:226.1222. IR (neat, cm
-1): υ 2931, 1650, 1596, 1496, 1397, 1212, 1029, 906, 726, 647。
在25 mL Schlenk试管中依次加入胺1ah
(0.2 mmol, 37.0 mg)、 2,3-丁二酮 (1.2 mmol, 103.3 mg)、乙醇
(95%, 0.5 mL);然后在40W白色LED照射下常规搅拌6小时后,反应体系用饱和亚硫酸钠溶液淬灭,用乙酸乙酯萃取3次,合并有机层,用无水硫酸钠干燥。用旋转蒸发仪除去溶剂、硅胶吸附,通过简单的柱层析即可得产物3ah,收率为80%。所制得产物的主要测试数据如下,通过分析可知,实际合成产物与理论分析一致。
1H NMR
(400 MHz, CDCl
3) δ 7.55 (d,
J
= 8.4 Hz, 2H), 7.10 (d,
J = 8.4 Hz, 2H), 3.25 (s, 3H), 1.88 (s, 3H).
13C
NMR (100 MHz, CDCl
3) δ
170.0, 143.4, 132.7, 128.6, 121.2, 36.9, 22.2. HRMS (ESI-TOF): Anal Calcd. For.
C
9H
10
79BrNO+H
+: 228.0019, Found:
228.0014; C
9H
10
81BrNO+H
+: 229.9998,
Found: 229.9994. IR (neat, cm
-1): υ
3395, 3060, 2932, 1649, 1587, 1484, 1371, 1179, 1084, 837, 722, 643。
Claims (10)
- 一种绿色的可见光催化的乙酰胺化合物的制备方法,其特征在于,在可见光照射下,以胺、酮为原料,反应制备乙酰胺化合物。
- 根据权利要求1所述绿色的可见光催化的乙酰胺化合物的制备方法,其特征在于,所述可见光为LED灯光。
- 根据权利要求1所述绿色的可见光催化的乙酰胺化合物的制备方法,其特征在于,反应的时间为4~12小时。
- 根据权利要求1所述绿色的可见光催化的乙酰胺化合物的制备方法,其特征在于,所述酮为2,3-丁二酮、1-苯基丙烷-1,2-二酮、2,3-戊二酮、2,3-己二酮或者丙酮。
- 根据权利要求1所述绿色的可见光催化的乙酰胺化合物的制备方法,其特征在于,反应在有机溶剂中进行。
- 根据权利要求6所述绿色的可见光催化的乙酰胺化合物的制备方法,其特征在于,所述有机溶剂为石油醚、1,2-二氯乙烷、1,1,1-三氯乙烷、1,1,2-三氯乙烷、硝基甲烷、乙腈、乙酸乙酯、丙酮、异丙醇或者95%乙醇。
- 根据权利要求1所述绿色的可见光催化的乙酰胺化合物的制备方法,其特征在于,酮的用量为胺摩尔量的5~7倍。
- 根据权利要求1所述绿色的可见光催化的乙酰胺化合物的制备方法制备的乙酰胺化合物。
- 以胺、酮为原料,在可见光照射下,反应制备乙酰胺化合物的应用。
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