WO2016141840A1 - Procédé de synthèse d'un composé intermédiaire pharmaceutique de phénanthrène dans un environnement d'hydroxyde de sodium - Google Patents
Procédé de synthèse d'un composé intermédiaire pharmaceutique de phénanthrène dans un environnement d'hydroxyde de sodium Download PDFInfo
- Publication number
- WO2016141840A1 WO2016141840A1 PCT/CN2016/075446 CN2016075446W WO2016141840A1 WO 2016141840 A1 WO2016141840 A1 WO 2016141840A1 CN 2016075446 W CN2016075446 W CN 2016075446W WO 2016141840 A1 WO2016141840 A1 WO 2016141840A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compound
- formula
- organic
- synthesizing
- phenanthrene
- Prior art date
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- VGBASMXDKFZLAK-UHFFFAOYSA-N CC1NCNC1 Chemical compound CC1NCNC1 VGBASMXDKFZLAK-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B37/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving either the formation of a carbon-to-carbon bond between two carbon atoms not directly linked already or the disconnection of two directly linked carbon atoms
- C07B37/10—Cyclisation
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/266—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions of hydrocarbons and halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
- C07C17/275—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of hydrocarbons and halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/42—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons homo- or co-oligomerisation with ring formation, not being a Diels-Alder conversion
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/86—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon
- C07C2/861—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only halogen as hetero-atoms
-
- 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
- C07D213/06—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 containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
- C07D213/16—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 containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing only one pyridine ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/20—Polycyclic condensed hydrocarbons
- C07C15/27—Polycyclic condensed hydrocarbons containing three rings
- C07C15/30—Phenanthrenes
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/18—Polycyclic aromatic halogenated hydrocarbons
- C07C25/22—Polycyclic aromatic halogenated hydrocarbons with condensed rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- C07C2531/22—Organic complexes
-
- 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
- C07D213/06—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 containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
- C07D213/127—Preparation from compounds containing pyridine rings
Definitions
- the present inventors have aimed to provide a novel catalytic synthesis method for phenanthrene compounds through a large number of experimental studies, and achieve the purpose of high yield and rapid reaction, and have a wide range of industrial application prospects.
- the halogen may be, for example, fluorine, chlorine, bromine or iodine.
- the molar ratio of the compound of the formula (II) to the compound of the formula (III) is 1:2-4, and may be, for example, 1:2, 1:3 or 1:4.
- the ligand L1 used is a ligand represented by the above formula L1 unless otherwise specified.
- a suitable solvent consisting of PEG-400 and 1-allyl-3-methylimidazolium tetrafluoroborate (1:0.3 by volume) was added to the reactor, and then replaced with nitrogen twice.
- the inside of the reactor was a nitrogen atmosphere; then 100 mmol of the compound of the above formula (II) 2-bromobiphenyl, 400 mmol of the compound of the above formula (III) 1-vinylnaphthalene, 3 mmol of PdCl 2 (dppf) and 12 mmol of copper hexafluorophosphate tetraacetonitrile were added.
- the composite catalyst, 20 mmol of ligand L1 and 300 mmol of diisopropylethanolamine were heated to 80 ° C with stirring and reacted at this temperature for 8 hours.
- Examples 25-28 Except that PdCl 2 (dppf) was replaced with bis(triphenylphosphine)palladium chloride (PdCl 2 (PPh 3 ) 2 ), respectively, the other operations were unchanged, and Examples 1-4 Examples 25-28 were carried out in the same manner.
- Examples 29-32 The operation was the same except that copper hexafluorophosphate tetraacetonitrile was replaced with copper triflate (Cu(OTf) 2 ), respectively, in the same manner as in Example 1-4. Examples 29-32 were implemented.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
La présente invention concerne un procédé de synthèse d'un composé de phénanthrène dans un environnement d'hydroxyde de sodium, le composé de phénanthrène étant présenté par la formule (I). Le procédé consiste à : sous un environnement de gaz inerte, lorsqu'un catalyseur, un ligand organique et de l'hydroxyde de sodium sont présents, faire réagir un composé de formule (II) et un composé de formule (III) dans un solvant pour obtenir un composé de formule (I), dans laquelle R1 et R2 représentent, indépendamment H, alkyle en C1-C6, alkyloxy en C1-C6 ou halogène. R3 représente aryle en C6-C10 ou hétéroaryle en C5-C8, éventuellement substitué par 1 à 3 groupes substituants et les groupes substituants sont alkyle en C1-C6 ou halogène. Le procédé permet d'obtenir un bon effet par la sélection d'un catalyseur, d'un ligand organique, d'une base et d'un solvant appropriés et présente de grandes perspectives pour des applications industrielles.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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CN201510100568.5A CN104692986B (zh) | 2015-03-06 | 2015-03-06 | 一种医药中间体菲类化合物的合成方法 |
CN201510100568.5 | 2015-03-06 |
Publications (1)
Publication Number | Publication Date |
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WO2016141840A1 true WO2016141840A1 (fr) | 2016-09-15 |
Family
ID=53340585
Family Applications (22)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2016/075403 WO2016141826A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un composé de phénanthrène intermédiaire pharmaceutique dans un environnement tert-butoxyde de potassium |
PCT/CN2016/075438 WO2016141838A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement de carbonate de sodium |
PCT/CN2016/075449 WO2016141841A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement d'hydroxyde de potassium |
PCT/CN2016/075402 WO2016141825A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, dans un environnement d'acétate de sodium |
PCT/CN2016/075452 WO2016141842A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un composé de phénanthrène intermédiaire pharmaceutique dans un environnement de phosphate de potassium |
PCT/CN2016/075437 WO2016141837A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène faisant appel à l'acétate de cuivre |
PCT/CN2016/075417 WO2016141832A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, à l'aide de pdcl2(cod) |
PCT/CN2016/075401 WO2016141824A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, dans un environnement d'acétate de sodium |
PCT/CN2016/075414 WO2016141829A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, à l'aide d'acétate de palladium |
PCT/CN2016/075413 WO2016141828A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux |
PCT/CN2016/075400 WO2016141823A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, dans un environnement de bicarbonate de potassium |
PCT/CN2016/075434 WO2016141834A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un composé phénanthrène, intermédiaire pharmaceutique, à l'aide de pdcl2(pph3)2 |
PCT/CN2016/075454 WO2016141844A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement de bicarbonate de sodium |
PCT/CN2016/075453 WO2016141843A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement de phosphate de sodium |
PCT/CN2016/075446 WO2016141840A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un composé intermédiaire pharmaceutique de phénanthrène dans un environnement d'hydroxyde de sodium |
PCT/CN2016/075436 WO2016141836A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène faisant appel à un acétylacétonate de cuivre |
PCT/CN2016/075416 WO2016141831A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires pharmaceutiques, à l'aide d'acétylacétonate de palladium |
PCT/CN2016/075435 WO2016141835A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène faisant appel à un trifluométhanesulfonate de cuivre |
PCT/CN2016/075415 WO2016141830A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé d'application de chlorure de palladium pour synthétiser un composé de phénanthrène interméaire pharmaceutique |
PCT/CN2016/075404 WO2016141827A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène en présence de diisopropylamine |
PCT/CN2016/075439 WO2016141839A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement de carbonate de potassium |
PCT/CN2016/075418 WO2016141833A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, à l'aide de trifluoroacétate de palladium |
Family Applications Before (14)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2016/075403 WO2016141826A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un composé de phénanthrène intermédiaire pharmaceutique dans un environnement tert-butoxyde de potassium |
PCT/CN2016/075438 WO2016141838A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement de carbonate de sodium |
PCT/CN2016/075449 WO2016141841A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement d'hydroxyde de potassium |
PCT/CN2016/075402 WO2016141825A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, dans un environnement d'acétate de sodium |
PCT/CN2016/075452 WO2016141842A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un composé de phénanthrène intermédiaire pharmaceutique dans un environnement de phosphate de potassium |
PCT/CN2016/075437 WO2016141837A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène faisant appel à l'acétate de cuivre |
PCT/CN2016/075417 WO2016141832A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, à l'aide de pdcl2(cod) |
PCT/CN2016/075401 WO2016141824A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, dans un environnement d'acétate de sodium |
PCT/CN2016/075414 WO2016141829A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, à l'aide d'acétate de palladium |
PCT/CN2016/075413 WO2016141828A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux |
PCT/CN2016/075400 WO2016141823A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, dans un environnement de bicarbonate de potassium |
PCT/CN2016/075434 WO2016141834A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un composé phénanthrène, intermédiaire pharmaceutique, à l'aide de pdcl2(pph3)2 |
PCT/CN2016/075454 WO2016141844A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement de bicarbonate de sodium |
PCT/CN2016/075453 WO2016141843A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement de phosphate de sodium |
Family Applications After (7)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CN2016/075436 WO2016141836A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène faisant appel à un acétylacétonate de cuivre |
PCT/CN2016/075416 WO2016141831A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires pharmaceutiques, à l'aide d'acétylacétonate de palladium |
PCT/CN2016/075435 WO2016141835A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène faisant appel à un trifluométhanesulfonate de cuivre |
PCT/CN2016/075415 WO2016141830A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé d'application de chlorure de palladium pour synthétiser un composé de phénanthrène interméaire pharmaceutique |
PCT/CN2016/075404 WO2016141827A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène en présence de diisopropylamine |
PCT/CN2016/075439 WO2016141839A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse d'un intermédiaire pharmaceutique de type composé de phénanthrène dans un environnement de carbonate de potassium |
PCT/CN2016/075418 WO2016141833A1 (fr) | 2015-03-06 | 2016-03-03 | Procédé de synthèse de composés phénanthrène, intermédiaires médicaux, à l'aide de trifluoroacétate de palladium |
Country Status (2)
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CN (3) | CN105801338B (fr) |
WO (22) | WO2016141826A1 (fr) |
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US9996386B2 (en) | 2014-07-23 | 2018-06-12 | Intel Corporation | Mid-thread pre-emption with software assisted context switch |
CN105801338B (zh) * | 2015-03-06 | 2018-08-14 | 胡淑婷 | 一种应用乙酰丙酮钯合成医药中间体菲类化合物的方法 |
CN105153152B (zh) * | 2015-08-28 | 2017-06-13 | 泉州奔众空气过滤网有限公司 | 一种咪唑类稠环化合物的合成方法 |
Citations (2)
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CN102827077A (zh) * | 2012-09-07 | 2012-12-19 | 浙江大学 | 一种菲啶衍生物的制备方法 |
CN104692986A (zh) * | 2015-03-06 | 2015-06-10 | 翟学研 | 一种医药中间体菲类化合物的合成方法 |
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2015
- 2015-03-06 CN CN201610216414.7A patent/CN105801338B/zh active Active
- 2015-03-06 CN CN201610216366.1A patent/CN105801336A/zh not_active Withdrawn
- 2015-03-06 CN CN201510100568.5A patent/CN104692986B/zh active Active
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2016
- 2016-03-03 WO PCT/CN2016/075403 patent/WO2016141826A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075438 patent/WO2016141838A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075449 patent/WO2016141841A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075402 patent/WO2016141825A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075452 patent/WO2016141842A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075437 patent/WO2016141837A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075417 patent/WO2016141832A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075401 patent/WO2016141824A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075414 patent/WO2016141829A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075413 patent/WO2016141828A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075400 patent/WO2016141823A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075434 patent/WO2016141834A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075454 patent/WO2016141844A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075453 patent/WO2016141843A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075446 patent/WO2016141840A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075436 patent/WO2016141836A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075416 patent/WO2016141831A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075435 patent/WO2016141835A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075415 patent/WO2016141830A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075404 patent/WO2016141827A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075439 patent/WO2016141839A1/fr active Application Filing
- 2016-03-03 WO PCT/CN2016/075418 patent/WO2016141833A1/fr active Application Filing
Patent Citations (2)
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CN102827077A (zh) * | 2012-09-07 | 2012-12-19 | 浙江大学 | 一种菲啶衍生物的制备方法 |
CN104692986A (zh) * | 2015-03-06 | 2015-06-10 | 翟学研 | 一种医药中间体菲类化合物的合成方法 |
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WO2016141823A1 (fr) | 2016-09-15 |
WO2016141836A1 (fr) | 2016-09-15 |
WO2016141844A1 (fr) | 2016-09-15 |
WO2016141842A1 (fr) | 2016-09-15 |
WO2016141837A1 (fr) | 2016-09-15 |
WO2016141828A1 (fr) | 2016-09-15 |
WO2016141830A1 (fr) | 2016-09-15 |
CN104692986A (zh) | 2015-06-10 |
WO2016141833A1 (fr) | 2016-09-15 |
CN105801336A (zh) | 2016-07-27 |
WO2016141824A1 (fr) | 2016-09-15 |
CN105801338A (zh) | 2016-07-27 |
WO2016141826A1 (fr) | 2016-09-15 |
WO2016141827A1 (fr) | 2016-09-15 |
WO2016141825A1 (fr) | 2016-09-15 |
CN105801338B (zh) | 2018-08-14 |
WO2016141832A1 (fr) | 2016-09-15 |
WO2016141835A1 (fr) | 2016-09-15 |
WO2016141834A1 (fr) | 2016-09-15 |
WO2016141843A1 (fr) | 2016-09-15 |
WO2016141831A1 (fr) | 2016-09-15 |
WO2016141841A1 (fr) | 2016-09-15 |
WO2016141839A1 (fr) | 2016-09-15 |
WO2016141829A1 (fr) | 2016-09-15 |
WO2016141838A1 (fr) | 2016-09-15 |
CN104692986B (zh) | 2016-05-25 |
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