CN106831867A - A kind of aryl oxidized phosphine P2Y12 receptor antagonists of cyano-thiophene and application thereof - Google Patents
A kind of aryl oxidized phosphine P2Y12 receptor antagonists of cyano-thiophene and application thereof Download PDFInfo
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- CN106831867A CN106831867A CN201710070042.6A CN201710070042A CN106831867A CN 106831867 A CN106831867 A CN 106831867A CN 201710070042 A CN201710070042 A CN 201710070042A CN 106831867 A CN106831867 A CN 106831867A
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- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 title abstract description 7
- 229940127424 P2Y12 Receptor Antagonists Drugs 0.000 title abstract description 6
- 125000003118 aryl group Chemical group 0.000 title abstract description 5
- 229910000073 phosphorus hydride Inorganic materials 0.000 title description 2
- CUPOOAWTRIURFT-UHFFFAOYSA-N thiophene-2-carbonitrile Chemical compound N#CC1=CC=CS1 CUPOOAWTRIURFT-UHFFFAOYSA-N 0.000 title description 2
- 208000007536 Thrombosis Diseases 0.000 claims abstract description 16
- 238000011282 treatment Methods 0.000 claims abstract description 11
- 239000003814 drug Substances 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims description 45
- 238000006243 chemical reaction Methods 0.000 claims description 9
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims description 4
- XGRJZXREYAXTGV-UHFFFAOYSA-N chlorodiphenylphosphine Chemical compound C=1C=CC=CC=1P(Cl)C1=CC=CC=C1 XGRJZXREYAXTGV-UHFFFAOYSA-N 0.000 claims description 4
- 239000000543 intermediate Substances 0.000 claims description 4
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 4
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 claims description 3
- 230000008859 change Effects 0.000 claims description 3
- -1 aryl lithium Chemical compound 0.000 claims description 2
- 150000002081 enamines Chemical class 0.000 claims description 2
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 239000007800 oxidant agent Substances 0.000 claims description 2
- 230000009467 reduction Effects 0.000 claims description 2
- 230000002194 synthesizing effect Effects 0.000 claims 1
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 abstract description 6
- 125000002560 nitrile group Chemical group 0.000 abstract description 3
- 229930192474 thiophene Natural products 0.000 abstract description 3
- 229940079593 drug Drugs 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 abstract description 2
- 238000003756 stirring Methods 0.000 description 14
- 238000000605 extraction Methods 0.000 description 12
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- XTWYTFMLZFPYCI-UHFFFAOYSA-N Adenosine diphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(O)=O)C(O)C1O XTWYTFMLZFPYCI-UHFFFAOYSA-N 0.000 description 7
- 210000004369 blood Anatomy 0.000 description 7
- XTWYTFMLZFPYCI-KQYNXXCUSA-N 5'-adenylphosphoric acid Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O XTWYTFMLZFPYCI-KQYNXXCUSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 102100026171 P2Y purinoceptor 12 Human genes 0.000 description 6
- 239000008280 blood Substances 0.000 description 6
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 238000010898 silica gel chromatography Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
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- 241000282414 Homo sapiens Species 0.000 description 5
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- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000002792 vascular Effects 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 208000005189 Embolism Diseases 0.000 description 3
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- 239000005552 B01AC04 - Clopidogrel Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 102100037600 P2Y purinoceptor 1 Human genes 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
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- 229960000583 acetic acid Drugs 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 230000008485 antagonism Effects 0.000 description 2
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- 229960003009 clopidogrel Drugs 0.000 description 2
- GKTWGGQPFAXNFI-HNNXBMFYSA-N clopidogrel Chemical compound C1([C@H](N2CC=3C=CSC=3CC2)C(=O)OC)=CC=CC=C1Cl GKTWGGQPFAXNFI-HNNXBMFYSA-N 0.000 description 2
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- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
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- 238000010792 warming Methods 0.000 description 2
- 206010003178 Arterial thrombosis Diseases 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 208000037260 Atherosclerotic Plaque Diseases 0.000 description 1
- PGOOKXHNNARJSC-WKTDWESFSA-N C/C=C(\C=C/C=C)/P(c1cc(C#N)c(CN2CCCCC2)[s]1)(c1ccccc1)=O Chemical compound C/C=C(\C=C/C=C)/P(c1cc(C#N)c(CN2CCCCC2)[s]1)(c1ccccc1)=O PGOOKXHNNARJSC-WKTDWESFSA-N 0.000 description 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N C1CCNCC1 Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
- NPVOXZBGVIJKNC-UHFFFAOYSA-N CC1C(C#N)=C(CN2CCCCC2)SC1P(c1ccccc1)(c1ccccc1)=O Chemical compound CC1C(C#N)=C(CN2CCCCC2)SC1P(c1ccccc1)(c1ccccc1)=O NPVOXZBGVIJKNC-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 208000024172 Cardiovascular disease Diseases 0.000 description 1
- 206010008088 Cerebral artery embolism Diseases 0.000 description 1
- 206010008190 Cerebrovascular accident Diseases 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
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- 206010011084 Coronary artery embolism Diseases 0.000 description 1
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- 108091006068 Gq proteins Proteins 0.000 description 1
- 102000052606 Gq-G11 GTP-Binding Protein alpha Subunits Human genes 0.000 description 1
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- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- 241000699660 Mus musculus Species 0.000 description 1
- NVQITKGOOWQJFS-UHFFFAOYSA-N N#Cc1c(C=O)[s]c(Cl)c1 Chemical compound N#Cc1c(C=O)[s]c(Cl)c1 NVQITKGOOWQJFS-UHFFFAOYSA-N 0.000 description 1
- SPTLXLAJDJGBFW-UHFFFAOYSA-N N#Cc1c(CN2CCCCC2)[s]c(Cl)c1 Chemical compound N#Cc1c(CN2CCCCC2)[s]c(Cl)c1 SPTLXLAJDJGBFW-UHFFFAOYSA-N 0.000 description 1
- 108050008996 P2Y purinoceptor 1 Proteins 0.000 description 1
- 208000018262 Peripheral vascular disease Diseases 0.000 description 1
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 description 1
- 102000003993 Phosphatidylinositol 3-kinases Human genes 0.000 description 1
- 102000007074 Phospholipase C beta Human genes 0.000 description 1
- 108010047834 Phospholipase C beta Proteins 0.000 description 1
- 208000010378 Pulmonary Embolism Diseases 0.000 description 1
- 108010014270 Purinergic P2Y12 Receptors Proteins 0.000 description 1
- 206010063544 Renal embolism Diseases 0.000 description 1
- 208000007718 Stable Angina Diseases 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- 201000007023 Thrombotic Thrombocytopenic Purpura Diseases 0.000 description 1
- 208000007814 Unstable Angina Diseases 0.000 description 1
- 206010047249 Venous thrombosis Diseases 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 206010000891 acute myocardial infarction Diseases 0.000 description 1
- 108060000200 adenylate cyclase Proteins 0.000 description 1
- 102000030621 adenylate cyclase Human genes 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 238000002399 angioplasty Methods 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 210000001367 artery Anatomy 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 238000013172 carotid endarterectomy Methods 0.000 description 1
- 208000026106 cerebrovascular disease Diseases 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 210000003040 circulating cell Anatomy 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 210000004351 coronary vessel Anatomy 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 208000009190 disseminated intravascular coagulation Diseases 0.000 description 1
- 208000002296 eclampsia Diseases 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 201000010849 intracranial embolism Diseases 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 230000010118 platelet activation Effects 0.000 description 1
- 201000011461 pre-eclampsia Diseases 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 229940002612 prodrug Drugs 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- DBDCNCCRPKTRSD-UHFFFAOYSA-N thieno[3,2-b]pyridine Chemical compound C1=CC=C2SC=CC2=N1 DBDCNCCRPKTRSD-UHFFFAOYSA-N 0.000 description 1
- 229940125670 thienopyridine Drugs 0.000 description 1
- 239000002175 thienopyridine Substances 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- 238000011830 transgenic mouse model Methods 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65586—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system at least one of the hetero rings does not contain nitrogen as ring hetero atom
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The present invention relates to the drug field related to angiocardiopathy.Specifically, the present invention relates to a kind of nitrile group-containing thiophene the P2Y12 receptor antagonists of aryl oxidized phosphine structure, its preparation method and its application of the treatment angiocardiopathy especially in thrombotic disease medicine is being prepared.
Description
Technical field
The present invention relates to the drug field for the treatment of cardiovascular disease.In particular it relates to outstanding to angiocardiopathy
It is that thrombotic disease has a kind of medicative P2Y12 receptor antagonists of the aryl oxidized phosphine structure of nitrile group-containing thiophene
Agent, Preparation Method And The Use.
Background technology
The medical complication relevant with there is thrombosis represents a kind of main cause of death.Some and development thrombus shape
Include that acute myocardial infarction, unstable angina pectoris and chronic stable angina pectoris, transience lack into relevant pathology example
Blood breaking-out, cerebrovas-cularaccident, peripheral vascular disease, pre-eclampsia and eclampsia, dvt formed, embolism (cerebral embolism,
Pulmonary embolism, coronary embolism, renal embolism etc.), disseminated intravascular coagulation or thrombotic thrombocytopenic purpura.Invading
Still there are the danger that thrombosis and ISR complication occur, the invasive surgical operation during and after entering property surgical operation
Such as angioplasty, carotid endarterectomy, aortocoronary by-pass grafting or support or the peace of vascular endoprostheses
Put.
Arterial thrombosis can occur after vascular damaged or atheromatous plaque rupture.Blood platelet is in these thrombus
Necessary effect is played in formation.Blood platelet can be by following substance activating：In blood flow circulating cells or along vascular wall present
The amboceptor that is discharged of damaging endothelial cell, or during injury of blood vessel exposed sub-endothelial matrix (such as collagen) blood
Bolt forms molecule.Additionally, blood platelet can also be observed such as in narrow blood vessel under the blood flow conditions with shearing force
As activate.After activation, the circulation platelet adhesion reaction is simultaneously accumulated at injury of blood vessel, forms thrombus.In this process, blood
Produced thrombus is sufficiently large volume to blood flow in pipe, so that it is partially or completely blocked.
In vein, thrombus can also be located to be formed slowly in obstruction or blood flow.Due to the property of these phlebothrombosises, it can be produced
The embolus moved in vascular system.These emboluses can thus block the blood flow in more remote blood vessel, the blood vessel such as lung
Artery or coronary artery.
Verified 5'- adenosine diphosphate (ADP)s (ADP) are platelet activation and the principal mediator assembled for many researchs, in thrombus
Played in the startup of formation and progress decisive role (Maffrand et al., Thromb.Haemostas., 1988,59,
225-230).ADP is discharged into circulation by the red blood cell and the endothelial cell of atherosclerosis wall for damaging, it is more specific and
Speech, as secreted by the activation blood platelet with compacted grains in place of very high concentration storage ADP.The platelet aggregation of ADP- inductions
The combination of two species specificity the purinergic receptor P2Y1 and P2Y12 by it and in the endoglin expression of human blood platelets is triggered.Institute
P2Y1 acceptors are stated, combine with stimulating through the PLC β of G α q, be responsible for mobilization, the change of platelet shape and in ADP that internal calcium is stored
On moment aggregation.The P2Y12, the activation of suppression and PI-3 kinases with the adenyl cyclase through G α i2 is combined, and is responsible for
The amplification of response and the stabilisation of aggregation.P2Y1-/- transgenic mice (Gachet et al., J.Clin.Invest., 1999,
104,1731-1737) proved with using for P2Y12-/- mouse (Conley et al., Nature, 2001,409,202-207)
Described two acceptors thrombus developing importance in vivo.In the mankind, P2Y12 gene defects and bleeding table are had been described above
Type is relevant with the notable decline of the platelet aggregation that ADP- is induced.Human clinical put into practice in use clopidogrel it has been proved that
The critical therapeutic strategy for the treatment of angiocardiopathy is represent by Antagonist block P2Y12 acceptors.Clopidogrel is thienopyridine
The prodrug of family, its active metabolite is covalently bond to P2Y12 acceptors, and cause internal biologically active pdgf can not retroactive inhibition
(Savi et al., Biochem.Biophys.Res.Commun., 2001,283,379-383), the medicine is in some clinical examinations
Middle its efficiency of display is tested, that is, is reduced dangerous patient and cardiovascular unexpected danger is occurred.
The invention discloses a kind of P2Y12 receptor antagonists of the aryl oxidized phosphine structure of nitrile group-containing thiophene, these compounds
Can be used to prepare the medicine for the treatment of angiocardiopathy especially thrombotic disease.
The content of the invention
It is an object of the present invention to provide a kind of P2Y12 receptor antagonists of the excellent activity with Formulas I.
Method it is a further object to provide the compound with Formulas I is prepared.
It is it is also another object of the present invention to provide the compound containing Formulas I as active ingredient and its cardiovascular in treatment
Disease application especially in terms of thrombotic disease.
Present invention is specifically described in conjunction with the purpose of the present invention.
Compound of the present invention with Formulas I has following structural formula：
Compound of formula I of the present invention can be synthesized by following route：
Compound II and compound III first react generation enamine intermediates, and the latter obtains compound IV by reduction；Chemical combination
Thing IV first at low temperature with n-BuLi treatment, the aryl lithium intermediate for obtaining again with diphenyl phosphine chloride reaction, obtain compound
V；Compound V oxidizer treatments obtain compound I.
Compound of formula I of the present invention has the antagonism of P2Y12 acceptors, can be used to prepare painstaking effort as active ingredient
Pipe disease especially thrombotic disease medicine.The activity of compound of formula I of the present invention is by external human blood blood
The suppression of platelet aggregation is tested to verify.
Compound of formula I of the invention is effective in comparatively wide dosage range.The dosage for example taken daily about exists
In the range of 1mg-700mg/ people, it is divided into and once or is for several times administered.The dosage for actually taking formula I can be by doctor's root
Determined according to relevant situation.
Specific embodiment
With reference to embodiment, the present invention is further illustrated.It should be noted that following embodiments are only for
Illustrate, and be not intended to limit the present invention.The various change that those skilled in the art's training centre of the invention is made all should
Within the protection domain required by the application claim.
The synthesis of the compound I-1 of embodiment 1
The synthesis of step 1. compound IV-1
Compound II (0.85g, 10mmol) and compound III-1 (1.47g, 10mmol) are dissolved in 10mL methyl alcohol, room temperature
Under be stirred overnight, then add NaCNBH3(1.26g, 20mmol), is stirred for 5 hours at room temperature, and TLC display reactions are completed.
Reactant mixture is carefully poured into 200mL frozen water, stirring, with 50mL × 3CH2Cl2Extraction, merges extraction phase, is washed with salt
Wash, anhydrous sodium sulfate drying.Suction filtration removes drier, and filtrate is evaporated on a rotary evaporator, and residue uses silica gel column chromatography
Purifying, obtains compound IV-1, white solid.ESI-MS, m/z=216 ([M+H]+)。
The synthesis of step 2. compound V-1
Compound IV-1 (1.29g, 6mmol) is dissolved in the dry THF of 15mL, stirring, and -78 are cooled in nitrogen atmosphere
DEG C, the hexane solution (3.75mL, 6mmol) of the n-BuLi of 1.6M is then slowly added dropwise with syringe, after completion of dropping, reaction
Mixture continues stirring 1 hour at such a temperature.Diphenyl phosphorus chloride (1.32g, 6mmol) is slowly added dropwise again with syringe to be dissolved in
The solution that the dry THF of 7mL are made, after completion of dropping, reactant mixture is stirred half an hour at such a temperature, is then warming up to room
Temperature is stirred for overnight.Reactant mixture is carefully poured into 200mL frozen water, stirring, with 50mL × 3CH2Cl2Extraction, merges extraction
Phase, uses salt water washing, anhydrous sodium sulfate drying.Suction filtration removes drier, and filtrate is evaporated on a rotary evaporator, and residue is used
Silica gel column chromatography is purified, and obtains compound V-1, white solid.ESI-MS, m/z=366 ([M+H]+)。
The synthesis of step 3. compound I-1
Compound V-1 (0.73g, 2mmol) is dissolved in 10mL glacial acetic acid, is stirred at room temperature, and 30% H is slowly added dropwise2O2Water
Solution (1mL), after completion of dropping, stirring was continued at room temperature overnight for reactant mixture, and TLC has found that reaction is completed.Reaction mixing
Thing is carefully poured into 200mL frozen water, stirring, with 50mL × 3CH2Cl2Extraction, merges extraction phase, uses salt water washing, anhydrous sulphur
Sour sodium is dried.Suction filtration removes drier, and filtrate is evaporated on a rotary evaporator, and residue is purified using silica gel column chromatography, is obtained
Compound I-1, white solid, 212-214 DEG C of fusing point, ESI-MS, m/z=382 ([M+H]+)。
The synthesis of the compound I-2 of embodiment 2
The synthesis of step 1. compound IV-2
Compound II (0.85g, 10mmol) and compound III-2 (1.71g, 10mmol) are dissolved in 10mL methyl alcohol, room temperature
Under be stirred overnight, then add NaCNBH3(1.26g, 20mmol), is stirred for 5 hours at room temperature, and TLC display reactions are completed.
Reactant mixture is carefully poured into 200mL frozen water, stirring, with 50mL × 3CH2Cl2Extraction, merges extraction phase, is washed with salt
Wash, anhydrous sodium sulfate drying.Suction filtration removes drier, and filtrate is evaporated on a rotary evaporator, and residue uses silica gel column chromatography
Purifying, obtains compound IV-2, white solid.ESI-MS, m/z=241 ([M+H]+)。
The synthesis of step 2. compound V-2
Compound IV-2 (1.45g, 6mmol) is dissolved in the dry THF of 15mL, stirring, and -78 are cooled in nitrogen atmosphere
DEG C, the hexane solution (3.75mL, 6mmol) of the n-BuLi of 1.6M is then slowly added dropwise with syringe, after completion of dropping, reaction
Mixture continues stirring 1 hour at such a temperature.Diphenyl phosphorus chloride (1.32g, 6mmol) is slowly added dropwise again with syringe to be dissolved in
The solution that the dry THF of 7mL are made, after completion of dropping, reactant mixture is stirred half an hour at such a temperature, is then warming up to room
Temperature is stirred for overnight.Reactant mixture is carefully poured into 200mL frozen water, stirring, with 50mL × 3CH2Cl2Extraction, merges extraction
Phase, uses salt water washing, anhydrous sodium sulfate drying.Suction filtration removes drier, and filtrate is evaporated on a rotary evaporator, and residue is used
Silica gel column chromatography is purified, and obtains compound V-2, white solid, ESI-MS, m/z=391 ([M+H]+)。
The synthesis of step 3. compound I-2
Compound V-2 (0.78g, 2mmol) is dissolved in 10mL glacial acetic acid, is stirred at room temperature, and 30% H is slowly added dropwise2O2Water
Solution (1mL), after completion of dropping, stirring was continued at room temperature overnight for reactant mixture, and TLC has found that reaction is completed.Reaction mixing
Thing is carefully poured into 200mL frozen water, stirring, with 50mL × 3CH2Cl2Extraction, merges extraction phase, uses salt water washing, anhydrous sulphur
Sour sodium is dried.Suction filtration removes drier, and filtrate is evaporated on a rotary evaporator, and residue is purified using silica gel column chromatography, is obtained
Compound I-2, white solid, 186-187 DEG C of fusing point, ESI-MS, m/z=407 ([M+H]+)。
The Compound ira vitro of embodiment 3 is to the hematoblastic inhibitory action of human blood
Using the 20mL syringes of the sodium citrate buffered containing 2mL, blood is gathered from healthy volunteer.Blood is shifted
Into PA tube, and (100g) 5 minutes (not using the braking of centrifuge) is centrifuged in room temperature.Then supernatant richness is collected
Thrombocyte plasma (PRP), dilution, and carried out platelet count before aggregation measurement is used it for.
37 DEG C of measurements (platelet aggregation instrument) for carrying out platelet aggregation in glass tube.By 4 μ L test compounds (than needing
The DMSO solution of dense 100 times of the final concentration wanted) mix with the PRP of 392 μ L brand-news, and be incubated 1 minute with stirring.Then to mixed
The ADP solution of 250 μM of 4 μ L is added in compound.Lasting stirring, by the method recording light variable density according to G.V.R.Born
(Born, Nature, 1962,194,927), monitors the measurement of aggregation 6 to 8 minutes.Use the aggregation amplitude meter represented with height
Result is calculated, and is represented with suppression percentage.(inhibition on platelet aggregation) IC of the compounds of this invention50It is as shown in the table.
| Compound | |
| The compound of embodiment 1 | 328 |
| The compound of embodiment 2 | 63 |
Can be seen that compound of the invention from upper table result has very strong antagonism to P2Y12, can be as system
The medicine of standby treatment angiocardiopathy especially thrombotic disease.
Claims (3)
1. there is the compound of Formulas I structure,
2. the method for synthesizing compound described in claim 1：
Compound II and compound III first react generation enamine intermediates, and the latter obtains compound IV by reduction；Compound IV
First at low temperature with n-BuLi treatment, the aryl lithium intermediate for obtaining again with diphenyl phosphine chloride reaction, obtain compound V；Change
Compound V oxidizer treatments obtain compound I.
3. application of the compound described in claim 1 in terms for the treatment of thrombotic disease medicine is prepared.
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN101868469A (en) * | 2007-11-29 | 2010-10-20 | 埃科特莱茵药品有限公司 | Phosphonic acid derivates and their use as P2Y12 receptor antagonists |
| CN102405220A (en) * | 2009-04-22 | 2012-04-04 | 埃科特莱茵药品有限公司 | Thiazole derivatives and their use as p2y12 receptor antagonists |
| CN104447867A (en) * | 2013-09-17 | 2015-03-25 | 天士力控股集团有限公司 | Thienopiperidine derivative, preparation method and application thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101868469A (en) * | 2007-11-29 | 2010-10-20 | 埃科特莱茵药品有限公司 | Phosphonic acid derivates and their use as P2Y12 receptor antagonists |
| CN102405220A (en) * | 2009-04-22 | 2012-04-04 | 埃科特莱茵药品有限公司 | Thiazole derivatives and their use as p2y12 receptor antagonists |
| CN104447867A (en) * | 2013-09-17 | 2015-03-25 | 天士力控股集团有限公司 | Thienopiperidine derivative, preparation method and application thereof |
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