JP4727880B2 - Ｎ−ピラゾールａ２ａ受容体アゴニスト - Google Patents
Ｎ−ピラゾールａ２ａ受容体アゴニスト Download PDFInfo
- Publication number
- JP4727880B2 JP4727880B2 JP2001515876A JP2001515876A JP4727880B2 JP 4727880 B2 JP4727880 B2 JP 4727880B2 JP 2001515876 A JP2001515876 A JP 2001515876A JP 2001515876 A JP2001515876 A JP 2001515876A JP 4727880 B2 JP4727880 B2 JP 4727880B2
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- JP
- Japan
- Prior art keywords
- alkyl
- aryl
- group
- halo
- heteroaryl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 229940044601 receptor agonist Drugs 0.000 title description 5
- 239000000018 receptor agonist Substances 0.000 title description 5
- 101150051188 Adora2a gene Proteins 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims description 214
- 125000003118 aryl group Chemical group 0.000 claims description 175
- 125000001072 heteroaryl group Chemical group 0.000 claims description 109
- 125000005843 halogen group Chemical group 0.000 claims description 84
- 150000001875 compounds Chemical class 0.000 claims description 80
- 229910052739 hydrogen Inorganic materials 0.000 claims description 76
- 239000001257 hydrogen Substances 0.000 claims description 71
- 125000000623 heterocyclic group Chemical group 0.000 claims description 58
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 52
- 125000001424 substituent group Chemical group 0.000 claims description 50
- 230000024883 vasodilation Effects 0.000 claims description 37
- -1 CF 3 Chemical group 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 27
- 125000000304 alkynyl group Chemical group 0.000 claims description 23
- 125000003342 alkenyl group Chemical group 0.000 claims description 20
- 150000002431 hydrogen Chemical class 0.000 claims description 19
- 229910052799 carbon Inorganic materials 0.000 claims description 18
- 239000003814 drug Substances 0.000 claims description 12
- 125000003107 substituted aryl group Chemical group 0.000 claims description 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 7
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 7
- 125000006260 ethylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])C([H])([H])[H] 0.000 claims description 7
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 241000124008 Mammalia Species 0.000 claims description 6
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 6
- VPCVILCDKKECPL-VXHCAWKWSA-N (2r,3r,4s,5r)-2-[6-amino-2-[4-(4-methoxyphenyl)-1h-pyrazol-5-yl]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C1=CC(OC)=CC=C1C1=CNN=C1C1=NC(N)=C(N=CN2[C@H]3[C@@H]([C@H](O)[C@@H](CO)O3)O)C2=N1 VPCVILCDKKECPL-VXHCAWKWSA-N 0.000 claims description 5
- RCZJMXUMKREDMI-PZGKNFOESA-N (3R,4S,5R)-2-[6-amino-2-[4-(4-chlorophenyl)pyrazol-1-yl]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C1=NC=2C(N)=NC(N3N=CC(=C3)C=3C=CC(Cl)=CC=3)=NC=2N1C1O[C@H](CO)[C@@H](O)[C@H]1O RCZJMXUMKREDMI-PZGKNFOESA-N 0.000 claims description 5
- NLDXPPQYALPBFB-WOUKDFQISA-N 1-[6-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-2-yl]pyrazole-4-carboxylic acid Chemical compound C1=NC=2C(N)=NC(N3N=CC(=C3)C(O)=O)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O NLDXPPQYALPBFB-WOUKDFQISA-N 0.000 claims description 5
- 125000005842 heteroatom Chemical group 0.000 claims description 5
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- LZPZPHGJDAGEJZ-AKAIJSEGSA-N regadenoson Chemical compound C1=C(C(=O)NC)C=NN1C1=NC(N)=C(N=CN2[C@H]3[C@@H]([C@H](O)[C@@H](CO)O3)O)C2=N1 LZPZPHGJDAGEJZ-AKAIJSEGSA-N 0.000 claims description 5
- HGPFIABPLAGCNQ-ORXWAGORSA-N 1-[6-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-2-yl]-n,n-dimethylpyrazole-4-carboxamide Chemical compound C1=C(C(=O)N(C)C)C=NN1C1=NC(N)=C(N=CN2[C@H]3[C@@H]([C@H](O)[C@@H](CO)O3)O)C2=N1 HGPFIABPLAGCNQ-ORXWAGORSA-N 0.000 claims description 4
- NQRSQXXWXGXYDU-HTVVRFAVSA-N 1-[6-amino-9-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-2-yl]pyrazole-4-carboxamide Chemical compound C1=C(C(=O)N)C=NN1C1=NC(N)=C(N=CN2[C@H]3[C@@H]([C@H](O)[C@@H](CO)O3)O)C2=N1 NQRSQXXWXGXYDU-HTVVRFAVSA-N 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 230000004936 stimulating effect Effects 0.000 claims description 4
- 238000006467 substitution reaction Methods 0.000 claims description 4
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 2
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- 230000037396 body weight Effects 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 125000004545 purin-9-yl group Chemical group N1=CN=C2N(C=NC2=C1)* 0.000 claims 1
- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 description 59
- 229940126142 compound 16 Drugs 0.000 description 59
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- 239000000556 agonist Substances 0.000 description 54
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 description 50
- 239000002126 C01EB10 - Adenosine Substances 0.000 description 33
- 229960005305 adenosine Drugs 0.000 description 29
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
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- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 17
- 125000000753 cycloalkyl group Chemical group 0.000 description 17
- 239000003379 purinergic P1 receptor agonist Substances 0.000 description 17
- 102000005962 receptors Human genes 0.000 description 17
- 108020003175 receptors Proteins 0.000 description 17
- 125000003545 alkoxy group Chemical group 0.000 description 16
- 125000004414 alkyl thio group Chemical group 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- PAOANWZGLPPROA-RQXXJAGISA-N CGS-21680 Chemical compound O[C@@H]1[C@H](O)[C@@H](C(=O)NCC)O[C@H]1N1C2=NC(NCCC=3C=CC(CCC(O)=O)=CC=3)=NC(N)=C2N=C1 PAOANWZGLPPROA-RQXXJAGISA-N 0.000 description 15
- 125000004104 aryloxy group Chemical group 0.000 description 15
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 14
- 241001465754 Metazoa Species 0.000 description 14
- 238000002474 experimental method Methods 0.000 description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 14
- 239000012528 membrane Substances 0.000 description 14
- FFBDFADSZUINTG-UHFFFAOYSA-N DPCPX Chemical compound N1C=2C(=O)N(CCC)C(=O)N(CCC)C=2N=C1C1CCCC1 FFBDFADSZUINTG-UHFFFAOYSA-N 0.000 description 13
- 230000009471 action Effects 0.000 description 13
- 229910052736 halogen Inorganic materials 0.000 description 13
- 230000001404 mediated effect Effects 0.000 description 13
- 229910052757 nitrogen Inorganic materials 0.000 description 13
- 238000002360 preparation method Methods 0.000 description 13
- 235000002639 sodium chloride Nutrition 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- 150000002367 halogens Chemical class 0.000 description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 12
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- 230000001746 atrial effect Effects 0.000 description 11
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 11
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- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/338,185 US6403567B1 (en) | 1999-06-22 | 1999-06-22 | N-pyrazole A2A adenosine receptor agonists |
| US09/338,185 | 1999-06-22 | ||
| PCT/US2000/040281 WO2000078779A2 (en) | 1999-06-22 | 2000-06-21 | N-pyrazole a2a receptor agonists |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003506461A JP2003506461A (ja) | 2003-02-18 |
| JP2003506461A5 JP2003506461A5 (US20050276830A1-20051215-C00018.png) | 2007-08-09 |
| JP4727880B2 true JP4727880B2 (ja) | 2011-07-20 |
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| JP2001515876A Expired - Lifetime JP4727880B2 (ja) | 1999-06-22 | 2000-06-21 | Ｎ−ピラゾールａ２ａ受容体アゴニスト |
Country Status (27)
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