JP2011504497A5 - - Google Patents
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- Publication number
- JP2011504497A5 JP2011504497A5 JP2010534916A JP2010534916A JP2011504497A5 JP 2011504497 A5 JP2011504497 A5 JP 2011504497A5 JP 2010534916 A JP2010534916 A JP 2010534916A JP 2010534916 A JP2010534916 A JP 2010534916A JP 2011504497 A5 JP2011504497 A5 JP 2011504497A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- amino
- acetate
- phenyl
- pentylamino
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 35
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 25
- -1 cyano, hydroxyl Chemical group 0.000 claims 23
- RUZLIIJDZBWWSA-INIZCTEOSA-N methyl 2-[[(1s)-1-(7-methyl-2-morpholin-4-yl-4-oxopyrido[1,2-a]pyrimidin-9-yl)ethyl]amino]benzoate Chemical group COC(=O)C1=CC=CC=C1N[C@@H](C)C1=CC(C)=CN2C(=O)C=C(N3CCOCC3)N=C12 RUZLIIJDZBWWSA-INIZCTEOSA-N 0.000 claims 14
- 150000003839 salts Chemical class 0.000 claims 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 11
- 229910052736 halogen Inorganic materials 0.000 claims 10
- 150000002367 halogens Chemical class 0.000 claims 9
- 125000000623 heterocyclic group Chemical group 0.000 claims 9
- 125000001424 substituent group Chemical group 0.000 claims 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- BYZABNXKJHIPDN-UHFFFAOYSA-N 4-(dimethylamino)butyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OCCCCN(C)C)C=C1 BYZABNXKJHIPDN-UHFFFAOYSA-N 0.000 claims 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 6
- 229910052760 oxygen Inorganic materials 0.000 claims 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 229910052717 sulfur Inorganic materials 0.000 claims 5
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 239000001301 oxygen Substances 0.000 claims 4
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000002619 bicyclic group Chemical group 0.000 claims 3
- 125000005843 halogen group Chemical group 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 3
- 125000002950 monocyclic group Chemical group 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 208000035143 Bacterial infection Diseases 0.000 claims 2
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 2
- 206010010744 Conjunctivitis allergic Diseases 0.000 claims 2
- 206010012438 Dermatitis atopic Diseases 0.000 claims 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 206010039085 Rhinitis allergic Diseases 0.000 claims 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims 2
- 208000002205 allergic conjunctivitis Diseases 0.000 claims 2
- 201000010105 allergic rhinitis Diseases 0.000 claims 2
- 208000006673 asthma Diseases 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 208000024998 atopic conjunctivitis Diseases 0.000 claims 2
- 201000008937 atopic dermatitis Diseases 0.000 claims 2
- 208000022362 bacterial infectious disease Diseases 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 208000006454 hepatitis Diseases 0.000 claims 2
- 231100000283 hepatitis Toxicity 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- VSFWCPUMFWQQEE-UHFFFAOYSA-N (1-methylpiperidin-4-yl)methyl 2-[3-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-4-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC(CC(=O)OCC2CCN(C)CC2)=CC=C1OC VSFWCPUMFWQQEE-UHFFFAOYSA-N 0.000 claims 1
- TZVVODMWZXRQIJ-UHFFFAOYSA-N (1-methylpiperidin-4-yl)methyl 2-[3-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=CC(CC(=O)OCC2CCN(C)CC2)=C1 TZVVODMWZXRQIJ-UHFFFAOYSA-N 0.000 claims 1
- JSBYGNLUEWJVOE-UHFFFAOYSA-N (1-methylpiperidin-4-yl)methyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-hydroxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC(C(=C1)O)=CC=C1CC(=O)OCC1CCN(C)CC1 JSBYGNLUEWJVOE-UHFFFAOYSA-N 0.000 claims 1
- WHHYIHVELBUKCN-UHFFFAOYSA-N (1-methylpiperidin-4-yl)methyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC(C(=C1)OC)=CC=C1CC(=O)OCC1CCN(C)CC1 WHHYIHVELBUKCN-UHFFFAOYSA-N 0.000 claims 1
- IVBJQWBZUWGOLK-UHFFFAOYSA-N (1-methylpiperidin-4-yl)methyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC(C=C1)=CC=C1CC(=O)OCC1CCN(C)CC1 IVBJQWBZUWGOLK-UHFFFAOYSA-N 0.000 claims 1
- DKRNYHYMUISKST-NRFANRHFSA-N (1-methylpiperidin-4-yl)methyl 2-[4-[[2-amino-4-[[(2s)-1-hydroxypentan-2-yl]amino]-6-methylpyrimidin-5-yl]methyl]-3-hydroxyphenyl]acetate Chemical compound CCC[C@@H](CO)NC1=NC(N)=NC(C)=C1CC(C(=C1)O)=CC=C1CC(=O)OCC1CCN(C)CC1 DKRNYHYMUISKST-NRFANRHFSA-N 0.000 claims 1
- VYLRUZOQUXMGDS-UHFFFAOYSA-N (1-methylpiperidin-4-yl)methyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC(C=C1)=CC=C1CC(=O)OCC1CCN(C)CC1 VYLRUZOQUXMGDS-UHFFFAOYSA-N 0.000 claims 1
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims 1
- 125000006699 (C1-C3) hydroxyalkyl group Chemical group 0.000 claims 1
- 125000004484 1-methylpiperidin-4-yl group Chemical group CN1CCC(CC1)* 0.000 claims 1
- KJBVRNQINPTFRU-UHFFFAOYSA-N 2-(1-methylpiperidin-4-yl)ethyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC(C=C1)=CC=C1CC(=O)OCCC1CCN(C)CC1 KJBVRNQINPTFRU-UHFFFAOYSA-N 0.000 claims 1
- JZCKKOIBKLTZBS-UHFFFAOYSA-N 2-(4-methyl-1,3-thiazol-5-yl)ethyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC(C(=C1)OC)=CC=C1CC(=O)OCCC1=C(C)N=CS1 JZCKKOIBKLTZBS-UHFFFAOYSA-N 0.000 claims 1
- DMNPBOQSEXIFDT-UHFFFAOYSA-N 2-(4-methylpiperazin-1-yl)ethyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC(C=C1)=CC=C1CC(=O)OCCN1CCN(C)CC1 DMNPBOQSEXIFDT-UHFFFAOYSA-N 0.000 claims 1
- XPQGDFIMNJFDAE-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OCCN(C)C)C=C1 XPQGDFIMNJFDAE-UHFFFAOYSA-N 0.000 claims 1
- NODMYIIFUPVNHX-UHFFFAOYSA-N 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetic acid Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(O)=O)C=C1 NODMYIIFUPVNHX-UHFFFAOYSA-N 0.000 claims 1
- CTBDABLNTBKPOJ-UHFFFAOYSA-N 2-hydroxyethyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OCCO)C=C1OC CTBDABLNTBKPOJ-UHFFFAOYSA-N 0.000 claims 1
- GISXEBIPMHPZOX-UHFFFAOYSA-N 3-(4-methylpiperazin-1-yl)propyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC(C=C1)=CC=C1CC(=O)OCCCN1CCN(C)CC1 GISXEBIPMHPZOX-UHFFFAOYSA-N 0.000 claims 1
- FXQAXZWSLMXANH-UHFFFAOYSA-N 3-(dimethylamino)propyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OCCCN(C)C)C=C1 FXQAXZWSLMXANH-UHFFFAOYSA-N 0.000 claims 1
- HJEDJKUWIHVYHM-UHFFFAOYSA-N 3-hydroxypropyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OCCCO)C=C1OC HJEDJKUWIHVYHM-UHFFFAOYSA-N 0.000 claims 1
- CRXIWMAAFKVAFF-UHFFFAOYSA-N 3-methylsulfonylpropyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OCCCS(C)(=O)=O)C=C1OC CRXIWMAAFKVAFF-UHFFFAOYSA-N 0.000 claims 1
- XXCBTNBISJVEMK-UHFFFAOYSA-N 4-(4-methylpiperazin-1-yl)butyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC(C=C1)=CC=C1CC(=O)OCCCCN1CCN(C)CC1 XXCBTNBISJVEMK-UHFFFAOYSA-N 0.000 claims 1
- MNVAEQPGCYDFTH-UHFFFAOYSA-N 4-(dimethylamino)butyl 2-[3-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-4-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC(CC(=O)OCCCCN(C)C)=CC=C1OC MNVAEQPGCYDFTH-UHFFFAOYSA-N 0.000 claims 1
- LBDLBLLLGLBLIK-UHFFFAOYSA-N 4-(dimethylamino)butyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-hydroxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OCCCCN(C)C)C=C1O LBDLBLLLGLBLIK-UHFFFAOYSA-N 0.000 claims 1
- DBUUCTYRHBFWBP-UHFFFAOYSA-N 4-[4-(dimethylamino)piperidin-1-yl]butyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC(C(=C1)OC)=CC=C1CC(=O)OCCCCN1CCC(N(C)C)CC1 DBUUCTYRHBFWBP-UHFFFAOYSA-N 0.000 claims 1
- UXAHLYRNZDNLHI-UHFFFAOYSA-N 4-[4-(dimethylamino)piperidin-1-yl]butyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC(C=C1)=CC=C1CC(=O)OCCCCN1CCC(N(C)C)CC1 UXAHLYRNZDNLHI-UHFFFAOYSA-N 0.000 claims 1
- PSFJKCHBPPPDNC-UHFFFAOYSA-N 4-hydroxybutyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OCCCCO)C=C1OC PSFJKCHBPPPDNC-UHFFFAOYSA-N 0.000 claims 1
- INPUDRNJVKURSZ-UHFFFAOYSA-N 4-pyrrolidin-1-ylbutyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-hydroxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC(C(=C1)O)=CC=C1CC(=O)OCCCCN1CCCC1 INPUDRNJVKURSZ-UHFFFAOYSA-N 0.000 claims 1
- 208000015898 Bacterial Skin disease Diseases 0.000 claims 1
- ZHCQROYXCQEBBP-UHFFFAOYSA-N C(C)(=O)OC1=CC=C(C=C1)CC=1C(=NC(=NC=1NCCCCC)N)C Chemical compound C(C)(=O)OC1=CC=C(C=C1)CC=1C(=NC(=NC=1NCCCCC)N)C ZHCQROYXCQEBBP-UHFFFAOYSA-N 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 1
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims 1
- 125000004406 C3-C8 cycloalkylene group Chemical group 0.000 claims 1
- 102000009410 Chemokine receptor Human genes 0.000 claims 1
- 108050000299 Chemokine receptor Proteins 0.000 claims 1
- 206010048768 Dermatosis Diseases 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 208000005176 Hepatitis C Diseases 0.000 claims 1
- 208000022361 Human papillomavirus infectious disease Diseases 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 claims 1
- ICWSJROJTWUNSE-UHFFFAOYSA-N NC1=NC(=C(C(=N1)C)CCCNS(=O)(=O)C=1N=CN(C1)C)NCCCCC Chemical compound NC1=NC(=C(C(=N1)C)CCCNS(=O)(=O)C=1N=CN(C1)C)NCCCCC ICWSJROJTWUNSE-UHFFFAOYSA-N 0.000 claims 1
- 108091000080 Phosphotransferase Proteins 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- SJUSUUSNSBJWMG-UHFFFAOYSA-N [1-(2-methoxyethyl)piperidin-4-yl]methyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC(C=C1)=CC=C1CC(=O)OCC1CCN(CCOC)CC1 SJUSUUSNSBJWMG-UHFFFAOYSA-N 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 239000000048 adrenergic agonist Substances 0.000 claims 1
- 229940126157 adrenergic receptor agonist Drugs 0.000 claims 1
- 239000000443 aerosol Substances 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 229940082638 cardiac stimulant phosphodiesterase inhibitors Drugs 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000000812 cholinergic antagonist Substances 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 229940112141 dry powder inhaler Drugs 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 239000003862 glucocorticoid Substances 0.000 claims 1
- 229940124750 glucocorticoid receptor agonist Drugs 0.000 claims 1
- 208000002672 hepatitis B Diseases 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- LIXABKAVBPBYBQ-UHFFFAOYSA-N methyl 2-[3-[2-[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propylamino]-2-oxoethyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCNC(=O)CC1=CC=CC(CC(=O)OC)=C1 LIXABKAVBPBYBQ-UHFFFAOYSA-N 0.000 claims 1
- RUFSKWZCEBXHCJ-UHFFFAOYSA-N methyl 2-[3-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-4-hydroxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC(CC(=O)OC)=CC=C1O RUFSKWZCEBXHCJ-UHFFFAOYSA-N 0.000 claims 1
- NDNZWYMPRYTKEJ-UHFFFAOYSA-N methyl 2-[3-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-4-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC(CC(=O)OC)=CC=C1OC NDNZWYMPRYTKEJ-UHFFFAOYSA-N 0.000 claims 1
- VILWGDTWJBRESJ-UHFFFAOYSA-N methyl 2-[3-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]-4-hydroxyphenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC(CC(=O)OC)=CC=C1O VILWGDTWJBRESJ-UHFFFAOYSA-N 0.000 claims 1
- RQDKMQLSRZDIQV-UHFFFAOYSA-N methyl 2-[3-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]-4-methoxyphenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC(CC(=O)OC)=CC=C1OC RQDKMQLSRZDIQV-UHFFFAOYSA-N 0.000 claims 1
- NESHMLZUUOVDJG-UHFFFAOYSA-N methyl 2-[3-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=CC(CC(=O)OC)=C1 NESHMLZUUOVDJG-UHFFFAOYSA-N 0.000 claims 1
- HFPDLDLMCGOPQT-UHFFFAOYSA-N methyl 2-[3-[[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propyl-[2-(dimethylamino)acetyl]amino]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCN(C(=O)CN(C)C)CC1=CC=CC(CC(=O)OC)=C1 HFPDLDLMCGOPQT-UHFFFAOYSA-N 0.000 claims 1
- RNGPSUUCDVRBHQ-UHFFFAOYSA-N methyl 2-[3-[[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propyl-[3-(dimethylamino)propanoyl]amino]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCN(C(=O)CCN(C)C)CC1=CC=CC(CC(=O)OC)=C1 RNGPSUUCDVRBHQ-UHFFFAOYSA-N 0.000 claims 1
- VUQWLQBFZLXNLL-UHFFFAOYSA-N methyl 2-[3-[[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propyl-[4-(dimethylamino)butanoyl]amino]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCN(C(=O)CCCN(C)C)CC1=CC=CC(CC(=O)OC)=C1 VUQWLQBFZLXNLL-UHFFFAOYSA-N 0.000 claims 1
- HIMJRJGIVBTRJC-UHFFFAOYSA-N methyl 2-[3-[[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propyl-methylsulfonylamino]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCN(S(C)(=O)=O)CC1=CC=CC(CC(=O)OC)=C1 HIMJRJGIVBTRJC-UHFFFAOYSA-N 0.000 claims 1
- FZEQIZYCEYZRRR-UHFFFAOYSA-N methyl 2-[3-[[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propylamino]methyl]phenoxy]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCNCC1=CC=CC(OCC(=O)OC)=C1 FZEQIZYCEYZRRR-UHFFFAOYSA-N 0.000 claims 1
- OFMDRXOBFRPNIK-UHFFFAOYSA-N methyl 2-[3-[[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propylamino]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCNCC1=CC=CC(CC(=O)OC)=C1 OFMDRXOBFRPNIK-UHFFFAOYSA-N 0.000 claims 1
- KRKWMWOXTBWQQJ-UHFFFAOYSA-N methyl 2-[3-[[4-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]butylamino]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCCNCC1=CC=CC(CC(=O)OC)=C1 KRKWMWOXTBWQQJ-UHFFFAOYSA-N 0.000 claims 1
- CZHMMVUCDGBBOT-UHFFFAOYSA-N methyl 2-[4-[2-[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propylamino]-2-oxoethyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCNC(=O)CC1=CC=C(CC(=O)OC)C=C1 CZHMMVUCDGBBOT-UHFFFAOYSA-N 0.000 claims 1
- FMVSYRYMESAHBX-UHFFFAOYSA-N methyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-hydroxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1O FMVSYRYMESAHBX-UHFFFAOYSA-N 0.000 claims 1
- WMRGREXQHLOXEC-UHFFFAOYSA-N methyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1OC WMRGREXQHLOXEC-UHFFFAOYSA-N 0.000 claims 1
- LTGWWJNPCNOBKY-UHFFFAOYSA-N methyl 2-[4-[[2-amino-4-(butylamino)-6-methylpyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1 LTGWWJNPCNOBKY-UHFFFAOYSA-N 0.000 claims 1
- KIJOGUHGFXYHIQ-HNNXBMFYSA-N methyl 2-[4-[[2-amino-4-[[(2s)-1-hydroxypentan-2-yl]amino]-6-methylpyrimidin-5-yl]methyl]-3-hydroxyphenyl]acetate Chemical compound CCC[C@@H](CO)NC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1O KIJOGUHGFXYHIQ-HNNXBMFYSA-N 0.000 claims 1
- TTYFFCJKAZFEPU-INIZCTEOSA-N methyl 2-[4-[[2-amino-4-[[(2s)-1-hydroxypentan-2-yl]amino]-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCC[C@@H](CO)NC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1OC TTYFFCJKAZFEPU-INIZCTEOSA-N 0.000 claims 1
- ZEZZVRSKTPRDHO-KRWDZBQOSA-N methyl 2-[4-[[2-amino-4-[[(3s)-1-hydroxyheptan-3-yl]amino]-6-methylpyrimidin-5-yl]methyl]-3-fluorophenyl]acetate Chemical compound CCCC[C@@H](CCO)NC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1F ZEZZVRSKTPRDHO-KRWDZBQOSA-N 0.000 claims 1
- IWSGKWLJZBEPNR-SFHVURJKSA-N methyl 2-[4-[[2-amino-4-[[(3s)-1-hydroxyheptan-3-yl]amino]-6-methylpyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCC[C@@H](CCO)NC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1OC IWSGKWLJZBEPNR-SFHVURJKSA-N 0.000 claims 1
- OHYUJDABQDCCFJ-UHFFFAOYSA-N methyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]-3-fluorophenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1F OHYUJDABQDCCFJ-UHFFFAOYSA-N 0.000 claims 1
- YWBUZOBEEKTTBM-UHFFFAOYSA-N methyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]-3-methoxyphenoxy]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(OCC(=O)OC)C=C1OC YWBUZOBEEKTTBM-UHFFFAOYSA-N 0.000 claims 1
- HIWQJYAWHHVTCG-UHFFFAOYSA-N methyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]-3-methoxyphenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1OC HIWQJYAWHHVTCG-UHFFFAOYSA-N 0.000 claims 1
- CGSDJZLYFVSPHW-UHFFFAOYSA-N methyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC1=CC=C(CC(=O)OC)C=C1 CGSDJZLYFVSPHW-UHFFFAOYSA-N 0.000 claims 1
- AWOUQNYJPWKMAF-NRFANRHFSA-N methyl 2-[4-[[3-[2-amino-4-[[(3s)-1-hydroxyheptan-3-yl]amino]-6-methylpyrimidin-5-yl]propylamino]methyl]phenyl]acetate Chemical compound CCCC[C@@H](CCO)NC1=NC(N)=NC(C)=C1CCCNCC1=CC=C(CC(=O)OC)C=C1 AWOUQNYJPWKMAF-NRFANRHFSA-N 0.000 claims 1
- WOSYEPNXYFTHBO-UHFFFAOYSA-N methyl 2-[4-[[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propylamino]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCNCC1=CC=C(CC(=O)OC)C=C1 WOSYEPNXYFTHBO-UHFFFAOYSA-N 0.000 claims 1
- FXQKFFLMHTYUFX-UHFFFAOYSA-N methyl 4-[3-[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]propyl-[[3-(2-methoxy-2-oxoethyl)phenyl]methyl]amino]-4-oxobutanoate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CCCN(C(=O)CCC(=O)OC)CC1=CC=CC(CC(=O)OC)=C1 FXQKFFLMHTYUFX-UHFFFAOYSA-N 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 230000000414 obstructive effect Effects 0.000 claims 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 claims 1
- 239000002571 phosphodiesterase inhibitor Substances 0.000 claims 1
- 102000020233 phosphotransferase Human genes 0.000 claims 1
- ZLUCFJCTDXPLIY-UHFFFAOYSA-N piperidin-4-ylmethyl 2-[4-[[2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl]methyl]phenyl]acetate Chemical compound CCCCCNC1=NC(N)=NC(C)=C1CC(C=C1)=CC=C1CC(=O)OCC1CCNCC1 ZLUCFJCTDXPLIY-UHFFFAOYSA-N 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 208000023504 respiratory system disease Diseases 0.000 claims 1
- 208000017520 skin disease Diseases 0.000 claims 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 229940037128 systemic glucocorticoids Drugs 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 0 *c1c(*)nc(N)nc1* Chemical compound *c1c(*)nc(N)nc1* 0.000 description 1
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| US61/013,699 | 2007-12-14 | ||
| PCT/SE2008/051334 WO2009067081A1 (en) | 2007-11-22 | 2008-11-21 | Pyrimidine derivatives for the treatment of asthma, copd, allergic rhinitis, allergic conjunctivitis, atopic dermatitis, cancer, hepatitis b, hepatitis c, hiv, hpv, bacterial infections and dermatosis |
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- 2008-11-21 CN CN2008801253753A patent/CN101925584B/zh not_active Expired - Fee Related
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