DE19752952A1 - Thienopyrimidine - Google Patents
ThienopyrimidineInfo
- Publication number
- DE19752952A1 DE19752952A1 DE19752952A DE19752952A DE19752952A1 DE 19752952 A1 DE19752952 A1 DE 19752952A1 DE 19752952 A DE19752952 A DE 19752952A DE 19752952 A DE19752952 A DE 19752952A DE 19752952 A1 DE19752952 A1 DE 19752952A1
- Authority
- DE
- Germany
- Prior art keywords
- pyrimidin
- chloro
- benzylamino
- benzothieno
- formula
- 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.)
- Withdrawn
Links
- 150000003839 salts Chemical class 0.000 claims abstract description 28
- 201000010099 disease Diseases 0.000 claims abstract description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 6
- 238000002560 therapeutic procedure Methods 0.000 claims abstract description 6
- -1 COOA Chemical group 0.000 claims description 91
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims description 44
- 150000001875 compounds Chemical class 0.000 claims description 43
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 13
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 12
- 125000002947 alkylene group Chemical group 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 6
- 239000003814 drug Substances 0.000 claims description 6
- IUEZNVXQJJMXHB-UHFFFAOYSA-N 3-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]propanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCC(O)=O)=NC2=C1C(CCCC1)=C1S2 IUEZNVXQJJMXHB-UHFFFAOYSA-N 0.000 claims description 5
- 201000001881 impotence Diseases 0.000 claims description 5
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 5
- 208000010228 Erectile Dysfunction Diseases 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000004185 ester group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- LYUPWDYILLXCBH-UHFFFAOYSA-N 4-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound C1CCCC2=C1C1=C(NCC=3C=C4OCOC4=CC=3)N=C(CCCC(=O)O)N=C1S2 LYUPWDYILLXCBH-UHFFFAOYSA-N 0.000 claims description 2
- MWRPZZKSUQYFQF-UHFFFAOYSA-N 4-[4-(1,3-benzodioxol-5-ylmethylamino)-6-methylthieno[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound C1=C2OCOC2=CC(CNC2=C3C=C(SC3=NC(CCCC(O)=O)=N2)C)=C1 MWRPZZKSUQYFQF-UHFFFAOYSA-N 0.000 claims description 2
- IAYPBSUFZUDVCB-UHFFFAOYSA-N 4-[4-[(3-chloro-4-methoxyphenyl)methylamino]-6-methylthieno[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCC(O)=O)=NC2=C1C=C(C)S2 IAYPBSUFZUDVCB-UHFFFAOYSA-N 0.000 claims description 2
- OGJAHBNONYXIQS-UHFFFAOYSA-N 5-[4-(1,3-benzodioxol-5-ylmethylamino)-6-methylthieno[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C1=C2OCOC2=CC(CNC2=C3C=C(SC3=NC(CCCCC(O)=O)=N2)C)=C1 OGJAHBNONYXIQS-UHFFFAOYSA-N 0.000 claims description 2
- PYHXQKPRNCIMHW-UHFFFAOYSA-N 5-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCCC(O)=O)=NC2=C1C(CCCC1)=C1S2 PYHXQKPRNCIMHW-UHFFFAOYSA-N 0.000 claims description 2
- CQPWMZYGLYAPAX-UHFFFAOYSA-N 7-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]heptanoic acid Chemical compound C1CCCC2=C1C1=C(NCC=3C=C4OCOC4=CC=3)N=C(CCCCCCC(=O)O)N=C1S2 CQPWMZYGLYAPAX-UHFFFAOYSA-N 0.000 claims description 2
- RFVAZPMINKWODA-UHFFFAOYSA-N 7-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]heptanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCCCCC(O)=O)=NC2=C1C(CCCC1)=C1S2 RFVAZPMINKWODA-UHFFFAOYSA-N 0.000 claims description 2
- 239000002552 dosage form Substances 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- 239000002590 phosphodiesterase V inhibitor Substances 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- IVKAATVWGBPOCV-UHFFFAOYSA-N 5-[4-[(3-chloro-4-methoxyphenyl)methylamino]-6-methylthieno[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCCC(O)=O)=NC2=C1C=C(C)S2 IVKAATVWGBPOCV-UHFFFAOYSA-N 0.000 claims 1
- 208000030499 combat disease Diseases 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 102000004861 Phosphoric Diester Hydrolases Human genes 0.000 abstract description 3
- 108090001050 Phosphoric Diester Hydrolases Proteins 0.000 abstract description 3
- 210000000748 cardiovascular system Anatomy 0.000 abstract description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 37
- 239000002253 acid Substances 0.000 description 19
- 239000004480 active ingredient Substances 0.000 description 15
- 150000002169 ethanolamines Chemical class 0.000 description 15
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 11
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- UUIQMZJEGPQKFD-UHFFFAOYSA-N Methyl butyrate Chemical compound CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 description 8
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 8
- XNCNNDVCAUWAIT-UHFFFAOYSA-N Methyl heptanoate Chemical compound CCCCCCC(=O)OC XNCNNDVCAUWAIT-UHFFFAOYSA-N 0.000 description 7
- HNBDRPTVWVGKBR-UHFFFAOYSA-N methyl pentanoate Chemical compound CCCCC(=O)OC HNBDRPTVWVGKBR-UHFFFAOYSA-N 0.000 description 7
- 235000019260 propionic acid Nutrition 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 6
- 239000003826 tablet Substances 0.000 description 6
- ZILSBZLQGRBMOR-UHFFFAOYSA-N 1,3-benzodioxol-5-ylmethanamine Chemical compound NCC1=CC=C2OCOC2=C1 ZILSBZLQGRBMOR-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 229940005605 valeric acid Drugs 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 235000011054 acetic acid Nutrition 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 125000004809 1-methylpropylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])[*:2] 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical group COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000012154 double-distilled water Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000012442 inert solvent Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 239000000829 suppository Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 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
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 229940031098 ethanolamine Drugs 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000010265 fast atom bombardment Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 2
- TWBYWOBDOCUKOW-UHFFFAOYSA-N isonicotinic acid Chemical compound OC(=O)C1=CC=NC=C1 TWBYWOBDOCUKOW-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 235000019359 magnesium stearate Nutrition 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- OLUCHMKPFHURIC-UHFFFAOYSA-N methyl 2-[4-(4-chloro-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl)cyclohexylidene]acetate Chemical compound C1CC(=CC(=O)OC)CCC1C1=NC(Cl)=C(C2=C(CCCC2)S2)C2=N1 OLUCHMKPFHURIC-UHFFFAOYSA-N 0.000 description 2
- XCCLUBXUFWORLI-UHFFFAOYSA-N methyl 3-(4-chloro-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl)propanoate Chemical compound C1CCCC2=C1C1=C(Cl)N=C(CCC(=O)OC)N=C1S2 XCCLUBXUFWORLI-UHFFFAOYSA-N 0.000 description 2
- QRHSYACAMCADHE-UHFFFAOYSA-N methyl 4-(4-chloro-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl)butanoate Chemical compound C1CCCC2=C1C1=C(Cl)N=C(CCCC(=O)OC)N=C1S2 QRHSYACAMCADHE-UHFFFAOYSA-N 0.000 description 2
- QSLBXQGEMZEFMR-UHFFFAOYSA-N methyl 5-(4,6-dichlorothieno[2,3-d]pyrimidin-2-yl)pentanoate Chemical compound COC(=O)CCCCC1=NC(Cl)=C2C=C(Cl)SC2=N1 QSLBXQGEMZEFMR-UHFFFAOYSA-N 0.000 description 2
- VZZPZAFCBNZLMQ-UHFFFAOYSA-N methyl 5-(4-chloro-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl)pentanoate Chemical compound C1CCCC2=C1C1=C(Cl)N=C(CCCCC(=O)OC)N=C1S2 VZZPZAFCBNZLMQ-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000002674 ointment Substances 0.000 description 2
- 150000007530 organic bases Chemical class 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229920001592 potato starch Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 235000012222 talc Nutrition 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- 230000000699 topical effect Effects 0.000 description 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- OCNMSDZALRAYEX-UHFFFAOYSA-N (3-chloro-4-methoxyphenyl)methanamine Chemical compound COC1=CC=C(CN)C=C1Cl OCNMSDZALRAYEX-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- RNHDAKUGFHSZEV-UHFFFAOYSA-N 1,4-dioxane;hydrate Chemical compound O.C1COCCO1 RNHDAKUGFHSZEV-UHFFFAOYSA-N 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical group CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 description 1
- 125000004818 1-methylbutylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000004837 1-methylpentylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000004825 2,2-dimethylpropylene group Chemical group [H]C([H])([H])C(C([H])([H])[H])(C([H])([H])[*:1])C([H])([H])[*:2] 0.000 description 1
- OXQGTIUCKGYOAA-UHFFFAOYSA-N 2-Ethylbutanoic acid Chemical compound CCC(CC)C(O)=O OXQGTIUCKGYOAA-UHFFFAOYSA-N 0.000 description 1
- HZNJATLOVGMBQB-UHFFFAOYSA-N 2-[4-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]cyclohexyl]acetic acid Chemical compound C1CC(CC(=O)O)CCC1C1=NC(NCC=2C=C3OCOC3=CC=2)=C(C2=C(CCCC2)S2)C2=N1 HZNJATLOVGMBQB-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 125000004819 2-methylbutylene group Chemical group [H]C([H])([H])C([H])(C([H])([H])[*:1])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- JMMZCWZIJXAGKW-UHFFFAOYSA-N 2-methylpent-2-ene Chemical group CCC=C(C)C JMMZCWZIJXAGKW-UHFFFAOYSA-N 0.000 description 1
- 125000004838 2-methylpentylene group Chemical group [H]C([H])([H])C([H])(C([H])([H])[*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000004810 2-methylpropylene group Chemical group [H]C([H])([H])C([H])(C([H])([H])[*:2])C([H])([H])[*:1] 0.000 description 1
- 102000001707 3',5'-Cyclic-AMP Phosphodiesterases Human genes 0.000 description 1
- 108010054479 3',5'-Cyclic-AMP Phosphodiesterases Proteins 0.000 description 1
- KOEFGZBWKWMLJX-UHFFFAOYSA-N 3-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]propanoic acid Chemical compound C1CCCC2=C1C1=C(NCC=3C=C4OCOC4=CC=3)N=C(CCC(=O)O)N=C1S2 KOEFGZBWKWMLJX-UHFFFAOYSA-N 0.000 description 1
- PIVGULNIFSXSFD-UHFFFAOYSA-N 3-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl]propanoic acid Chemical compound C1=C2OCOC2=CC(CNC=2N=C(CCC(O)=O)N=C3SC(=C(C3=2)C)C)=C1 PIVGULNIFSXSFD-UHFFFAOYSA-N 0.000 description 1
- UMJUUZGBJCGDNL-UHFFFAOYSA-N 3-[4-(1,3-benzodioxol-5-ylmethylamino)-6-chlorothieno[2,3-d]pyrimidin-2-yl]propanoic acid Chemical compound C1=C2OCOC2=CC(CNC=2N=C(N=C3SC(Cl)=CC3=2)CCC(=O)O)=C1 UMJUUZGBJCGDNL-UHFFFAOYSA-N 0.000 description 1
- KKZQOSGLZDDUGX-UHFFFAOYSA-N 3-[4-(1,3-benzodioxol-5-ylmethylamino)-6-ethylthieno[2,3-d]pyrimidin-2-yl]propanoic acid Chemical compound C1=C2OCOC2=CC(CNC2=C3C=C(SC3=NC(CCC(O)=O)=N2)CC)=C1 KKZQOSGLZDDUGX-UHFFFAOYSA-N 0.000 description 1
- XQNLBIDIGZJABQ-UHFFFAOYSA-N 3-[4-(1,3-benzodioxol-5-ylmethylamino)-6-methylthieno[2,3-d]pyrimidin-2-yl]propanoic acid Chemical compound C1=C2OCOC2=CC(CNC2=C3C=C(SC3=NC(CCC(O)=O)=N2)C)=C1 XQNLBIDIGZJABQ-UHFFFAOYSA-N 0.000 description 1
- ZWUQKYLMIKDRBN-UHFFFAOYSA-N 3-[4-(benzylamino)-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]propanoic acid Chemical compound C=12C=3CCCCC=3SC2=NC(CCC(=O)O)=NC=1NCC1=CC=CC=C1 ZWUQKYLMIKDRBN-UHFFFAOYSA-N 0.000 description 1
- JCKXGGJLRXFROE-UHFFFAOYSA-N 3-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]propanamide Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCC(N)=O)=NC2=C1C(CCCC1)=C1S2 JCKXGGJLRXFROE-UHFFFAOYSA-N 0.000 description 1
- IVPRGZDXVHWNSQ-UHFFFAOYSA-N 3-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]propanenitrile Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCC#N)=NC2=C1C(CCCC1)=C1S2 IVPRGZDXVHWNSQ-UHFFFAOYSA-N 0.000 description 1
- RELQKAVYWFHQSW-UHFFFAOYSA-N 3-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]propanoyl chloride Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCC(Cl)=O)=NC2=C1C(CCCC1)=C1S2 RELQKAVYWFHQSW-UHFFFAOYSA-N 0.000 description 1
- OFMBPHSYWIXKKK-UHFFFAOYSA-N 3-[4-[(3-chloro-4-methoxyphenyl)methylamino]-6-methylthieno[2,3-d]pyrimidin-2-yl]propanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCC(O)=O)=NC2=C1C=C(C)S2 OFMBPHSYWIXKKK-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- RRPPBGHUQJDYHW-UHFFFAOYSA-N 3-cyclohexylpropa-1,2-dienylcyclohexane Chemical group C1CCCCC1C=C=CC1CCCCC1 RRPPBGHUQJDYHW-UHFFFAOYSA-N 0.000 description 1
- 125000004820 3-methylbutylene group Chemical group [H]C([H])([H])C([H])(C([H])([H])[*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000004839 3-methylpentylene group Chemical group [H]C([H])([H])C([H])(C([H])([H])C([H])([H])[*:1])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- YTTJUDPVAWCXGY-UHFFFAOYSA-N 4-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound C1=C2OCOC2=CC(CNC=2N=C(CCCC(O)=O)N=C3SC(=C(C3=2)C)C)=C1 YTTJUDPVAWCXGY-UHFFFAOYSA-N 0.000 description 1
- ADJWVSWKCLXCJG-UHFFFAOYSA-N 4-[4-(1,3-benzodioxol-5-ylmethylamino)-6-chlorothieno[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound C1=C2OCOC2=CC(CNC=2N=C(N=C3SC(Cl)=CC3=2)CCCC(=O)O)=C1 ADJWVSWKCLXCJG-UHFFFAOYSA-N 0.000 description 1
- HHVNVUPVASEGRO-UHFFFAOYSA-N 4-[4-(1,3-benzodioxol-5-ylmethylamino)-6-ethylthieno[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound C1=C2OCOC2=CC(CNC2=C3C=C(SC3=NC(CCCC(O)=O)=N2)CC)=C1 HHVNVUPVASEGRO-UHFFFAOYSA-N 0.000 description 1
- NEPMGMTXWPYMGB-UHFFFAOYSA-N 4-[4-(benzylamino)-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound C=12C=3CCCCC=3SC2=NC(CCCC(=O)O)=NC=1NCC1=CC=CC=C1 NEPMGMTXWPYMGB-UHFFFAOYSA-N 0.000 description 1
- SQHRKIYCXMYGAV-UHFFFAOYSA-N 4-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCC(O)=O)=NC2=C1C(CCCC1)=C1S2 SQHRKIYCXMYGAV-UHFFFAOYSA-N 0.000 description 1
- LEJSDOVHSWAASG-UHFFFAOYSA-N 4-[4-[(3-chloro-4-methoxyphenyl)methylamino]-6-ethylthieno[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound N1=C(CCCC(O)=O)N=C2SC(CC)=CC2=C1NCC1=CC=C(OC)C(Cl)=C1 LEJSDOVHSWAASG-UHFFFAOYSA-N 0.000 description 1
- SRCRTSGCDCPTJU-UHFFFAOYSA-N 4-[6-chloro-4-[(3-chloro-4-methoxyphenyl)methylamino]thieno[2,3-d]pyrimidin-2-yl]butanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCC(O)=O)=NC2=C1C=C(Cl)S2 SRCRTSGCDCPTJU-UHFFFAOYSA-N 0.000 description 1
- 125000004840 4-methylpentylene group Chemical group [H]C([H])([H])C([H])(C([H])([H])[*:2])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- UHGMVOXYHYZDTQ-UHFFFAOYSA-N 5-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C1CCCC2=C1C1=C(NCC=3C=C4OCOC4=CC=3)N=C(CCCCC(=O)O)N=C1S2 UHGMVOXYHYZDTQ-UHFFFAOYSA-N 0.000 description 1
- YDWBHZVZCSACNW-UHFFFAOYSA-N 5-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C1=C2OCOC2=CC(CNC=2N=C(CCCCC(O)=O)N=C3SC(=C(C3=2)C)C)=C1 YDWBHZVZCSACNW-UHFFFAOYSA-N 0.000 description 1
- MZZNIAICOOXPDT-UHFFFAOYSA-N 5-[4-(1,3-benzodioxol-5-ylmethylamino)-6-chlorothieno[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C1=C2OCOC2=CC(CNC=2N=C(N=C3SC(Cl)=CC3=2)CCCCC(=O)O)=C1 MZZNIAICOOXPDT-UHFFFAOYSA-N 0.000 description 1
- NIBMPHCDSBWRAR-UHFFFAOYSA-N 5-[4-(1,3-benzodioxol-5-ylmethylamino)-6-ethylthieno[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C1=C2OCOC2=CC(CNC2=C3C=C(SC3=NC(CCCCC(O)=O)=N2)CC)=C1 NIBMPHCDSBWRAR-UHFFFAOYSA-N 0.000 description 1
- OWCDJDBAXPOLBE-UHFFFAOYSA-N 5-[4-(benzylamino)-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C=12C=3CCCCC=3SC2=NC(CCCCC(=O)O)=NC=1NCC1=CC=CC=C1 OWCDJDBAXPOLBE-UHFFFAOYSA-N 0.000 description 1
- FVHZBPZSSNEPBI-UHFFFAOYSA-N 5-[4-(benzylamino)-6-ethylthieno[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound N1=C(CCCCC(O)=O)N=C2SC(CC)=CC2=C1NCC1=CC=CC=C1 FVHZBPZSSNEPBI-UHFFFAOYSA-N 0.000 description 1
- IGDYANWDZANOGE-UHFFFAOYSA-N 5-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCCC(O)=O)=NC2=C1C(C)=C(C)S2 IGDYANWDZANOGE-UHFFFAOYSA-N 0.000 description 1
- HBEIUKLRJDDHPL-UHFFFAOYSA-N 5-[4-[(3-chloro-4-methoxyphenyl)methylamino]-6-ethylthieno[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound N1=C(CCCCC(O)=O)N=C2SC(CC)=CC2=C1NCC1=CC=C(OC)C(Cl)=C1 HBEIUKLRJDDHPL-UHFFFAOYSA-N 0.000 description 1
- KKYRHBZTGHAKRJ-UHFFFAOYSA-N 5-[6-chloro-4-[(3-chloro-4-methoxyphenyl)methylamino]thieno[2,3-d]pyrimidin-2-yl]pentanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCCC(O)=O)=NC2=C1C=C(Cl)S2 KKYRHBZTGHAKRJ-UHFFFAOYSA-N 0.000 description 1
- XYBVAYXQJOFPEK-UHFFFAOYSA-N 7-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl]heptanoic acid Chemical compound C1=C2OCOC2=CC(CNC=2N=C(CCCCCCC(O)=O)N=C3SC(=C(C3=2)C)C)=C1 XYBVAYXQJOFPEK-UHFFFAOYSA-N 0.000 description 1
- OPVIUFADGVCWFW-UHFFFAOYSA-N 7-[4-(1,3-benzodioxol-5-ylmethylamino)-6-chlorothieno[2,3-d]pyrimidin-2-yl]heptanoic acid Chemical compound C1=C2OCOC2=CC(CNC=2N=C(N=C3SC(Cl)=CC3=2)CCCCCCC(=O)O)=C1 OPVIUFADGVCWFW-UHFFFAOYSA-N 0.000 description 1
- HIVNAWWJIZUSMV-UHFFFAOYSA-N 7-[4-(1,3-benzodioxol-5-ylmethylamino)-6-ethylthieno[2,3-d]pyrimidin-2-yl]heptanoic acid Chemical compound C1=C2OCOC2=CC(CNC2=C3C=C(SC3=NC(CCCCCCC(O)=O)=N2)CC)=C1 HIVNAWWJIZUSMV-UHFFFAOYSA-N 0.000 description 1
- IHYIIUJPXFDZLK-UHFFFAOYSA-N 7-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl]heptanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCCCCC(O)=O)=NC2=C1C(C)=C(C)S2 IHYIIUJPXFDZLK-UHFFFAOYSA-N 0.000 description 1
- IPZSYFAAUREHQE-UHFFFAOYSA-N 7-[4-[(3-chloro-4-methoxyphenyl)methylamino]-6-ethylthieno[2,3-d]pyrimidin-2-yl]heptanoic acid Chemical compound N1=C(CCCCCCC(O)=O)N=C2SC(CC)=CC2=C1NCC1=CC=C(OC)C(Cl)=C1 IPZSYFAAUREHQE-UHFFFAOYSA-N 0.000 description 1
- RZGWAXCMWLUURN-UHFFFAOYSA-N 7-[4-[(3-chloro-4-methoxyphenyl)methylamino]-6-methylthieno[2,3-d]pyrimidin-2-yl]heptanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCCCCC(O)=O)=NC2=C1C=C(C)S2 RZGWAXCMWLUURN-UHFFFAOYSA-N 0.000 description 1
- QMIRUCHRBBYVHZ-UHFFFAOYSA-N 7-[6-chloro-4-[(3-chloro-4-methoxyphenyl)methylamino]thieno[2,3-d]pyrimidin-2-yl]heptanoic acid Chemical compound C1=C(Cl)C(OC)=CC=C1CNC1=NC(CCCCCCC(O)=O)=NC2=C1C=C(Cl)S2 QMIRUCHRBBYVHZ-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- OIAKHFGDGAJHIW-UHFFFAOYSA-N CC(C(=O)O)CCCC=1N=C(C2=C(N1)SC1=C2CCCC1)NCC1=CC2=C(C=C1)OCO2 Chemical compound CC(C(=O)O)CCCC=1N=C(C2=C(N1)SC1=C2CCCC1)NCC1=CC2=C(C=C1)OCO2 OIAKHFGDGAJHIW-UHFFFAOYSA-N 0.000 description 1
- JQIAVTZZHXGMHQ-UHFFFAOYSA-N COC(CCCC=1N=C(C2=C(N1)SC(=C2)C)NCC2=CC=CC=C2)=O.COC(CCCC=2N=C(C1=C(N2)SC(=C1)C)Cl)=O Chemical compound COC(CCCC=1N=C(C2=C(N1)SC(=C2)C)NCC2=CC=CC=C2)=O.COC(CCCC=2N=C(C1=C(N2)SC(=C1)C)Cl)=O JQIAVTZZHXGMHQ-UHFFFAOYSA-N 0.000 description 1
- GRYGEYLKDOBWQB-UHFFFAOYSA-N COC(CCCCC=1N=C(C2=C(N1)SC(=C2C)C)NCC2=CC(=C(C=C2)OC)Cl)=O.COC(CCCCC=2N=C(C1=C(N2)SC(=C1C)C)Cl)=O Chemical compound COC(CCCCC=1N=C(C2=C(N1)SC(=C2C)C)NCC2=CC(=C(C=C2)OC)Cl)=O.COC(CCCCC=2N=C(C1=C(N2)SC(=C1C)C)Cl)=O GRYGEYLKDOBWQB-UHFFFAOYSA-N 0.000 description 1
- JPVPLCXLXPXLNQ-UHFFFAOYSA-N COC(CCCCCCC=1N=C(C2=C(N1)SC(=C2)C)NCC2=CC(=C(C=C2)OC)Cl)=O.COC(CCCCCCC=2N=C(C1=C(N2)SC(=C1)C)Cl)=O Chemical compound COC(CCCCCCC=1N=C(C2=C(N1)SC(=C2)C)NCC2=CC(=C(C=C2)OC)Cl)=O.COC(CCCCCCC=2N=C(C1=C(N2)SC(=C1)C)Cl)=O JPVPLCXLXPXLNQ-UHFFFAOYSA-N 0.000 description 1
- LJLHISFJIWTXCI-UHFFFAOYSA-N COC(CCCCCCC=1N=C(C2=C(N1)SC(=C2)CC)NCC2=CC(=C(C=C2)OC)Cl)=O.COC(CCCCCCC=2N=C(C1=C(N2)SC(=C1)CC)Cl)=O Chemical compound COC(CCCCCCC=1N=C(C2=C(N1)SC(=C2)CC)NCC2=CC(=C(C=C2)OC)Cl)=O.COC(CCCCCCC=2N=C(C1=C(N2)SC(=C1)CC)Cl)=O LJLHISFJIWTXCI-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- XUDVUGJOHPVWGM-UHFFFAOYSA-N ClC=1C=C(CNC=2C3=C(N=C(N2)CCCCC(=O)OC)SC(=C3)C)C=CC1OC.ClC=1C3=C(N=C(N1)CCCCC(=O)OC)SC(=C3)C Chemical compound ClC=1C=C(CNC=2C3=C(N=C(N2)CCCCC(=O)OC)SC(=C3)C)C=CC1OC.ClC=1C3=C(N=C(N1)CCCCC(=O)OC)SC(=C3)C XUDVUGJOHPVWGM-UHFFFAOYSA-N 0.000 description 1
- RITPFQVCWTUSMO-UHFFFAOYSA-N ClC=1C=C(CNC=2C3=C(N=C(N2)CCCCC(=O)OC)SC(=C3)CC)C=CC1OC.ClC=1C3=C(N=C(N1)CCCCC(=O)OC)SC(=C3)CC Chemical compound ClC=1C=C(CNC=2C3=C(N=C(N2)CCCCC(=O)OC)SC(=C3)CC)C=CC1OC.ClC=1C3=C(N=C(N1)CCCCC(=O)OC)SC(=C3)CC RITPFQVCWTUSMO-UHFFFAOYSA-N 0.000 description 1
- NSTWEYURRJOLDZ-UHFFFAOYSA-N ClC=1C=C(CNC=2C3=C(N=C(N2)CCCCCCC(=O)OC)SC(=C3C)C)C=CC1OC.ClC=1C3=C(N=C(N1)CCCCCCC(=O)OC)SC(=C3C)C Chemical compound ClC=1C=C(CNC=2C3=C(N=C(N2)CCCCCCC(=O)OC)SC(=C3C)C)C=CC1OC.ClC=1C3=C(N=C(N1)CCCCCCC(=O)OC)SC(=C3C)C NSTWEYURRJOLDZ-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 206010019280 Heart failures Diseases 0.000 description 1
- LELOWRISYMNNSU-UHFFFAOYSA-N Hydrocyanic acid Natural products N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 1
- 206010021118 Hypotonia Diseases 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 210000005226 corpus cavernosum Anatomy 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 239000006196 drop Substances 0.000 description 1
- 239000000890 drug combination Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- AFAXGSQYZLGZPG-UHFFFAOYSA-N ethanedisulfonic acid Chemical compound OS(=O)(=O)CCS(O)(=O)=O AFAXGSQYZLGZPG-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 239000003889 eye drop Substances 0.000 description 1
- 229940012356 eye drops Drugs 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000007903 gelatin capsule Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 229940126601 medicinal product Drugs 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- DKYYKIHEIOOWRB-UHFFFAOYSA-N methyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate Chemical compound C1CCCC2=C1SC(N)=C2C(=O)OC DKYYKIHEIOOWRB-UHFFFAOYSA-N 0.000 description 1
- LROMJHRXOSOPCW-UHFFFAOYSA-N methyl 3-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]propanoate Chemical compound C=12C=3CCCCC=3SC2=NC(CCC(=O)OC)=NC=1NCC1=CC=C(OC)C(Cl)=C1 LROMJHRXOSOPCW-UHFFFAOYSA-N 0.000 description 1
- QRKDMITYUBLVQE-UHFFFAOYSA-N methyl 4-(4,6-dichlorothieno[2,3-d]pyrimidin-2-yl)butanoate Chemical compound COC(=O)CCCC1=NC(Cl)=C2C=C(Cl)SC2=N1 QRKDMITYUBLVQE-UHFFFAOYSA-N 0.000 description 1
- FOAVFHLOVVDTQD-UHFFFAOYSA-N methyl 4-(4-chloro-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)butanoate Chemical compound COC(=O)CCCC1=NC(Cl)=C2C(C)=C(C)SC2=N1 FOAVFHLOVVDTQD-UHFFFAOYSA-N 0.000 description 1
- VPURDSJEMRDJLH-UHFFFAOYSA-N methyl 4-(4-chloro-6-ethylthieno[2,3-d]pyrimidin-2-yl)butanoate Chemical compound N1=C(CCCC(=O)OC)N=C2SC(CC)=CC2=C1Cl VPURDSJEMRDJLH-UHFFFAOYSA-N 0.000 description 1
- DGABDUQGMPSQQR-UHFFFAOYSA-N methyl 4-(4-chloro-6-methylthieno[2,3-d]pyrimidin-2-yl)butanoate Chemical compound COC(=O)CCCC1=NC(Cl)=C2C=C(C)SC2=N1 DGABDUQGMPSQQR-UHFFFAOYSA-N 0.000 description 1
- LAGQMYRWDCDFQM-UHFFFAOYSA-N methyl 4-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl]butanoate methyl 4-(4-chloro-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)butanoate Chemical compound C1OC=2C=C(CNC=3C4=C(N=C(N3)CCCC(=O)OC)SC(=C4C)C)C=CC2O1.ClC=1C2=C(N=C(N1)CCCC(=O)OC)SC(=C2C)C LAGQMYRWDCDFQM-UHFFFAOYSA-N 0.000 description 1
- ILKOIBBRSZNPGH-UHFFFAOYSA-N methyl 4-[4-(1,3-benzodioxol-5-ylmethylamino)-6-ethylthieno[2,3-d]pyrimidin-2-yl]butanoate methyl 4-(4-chloro-6-ethylthieno[2,3-d]pyrimidin-2-yl)butanoate Chemical compound C1OC=2C=C(CNC=3C4=C(N=C(N3)CCCC(=O)OC)SC(=C4)CC)C=CC2O1.ClC=1C2=C(N=C(N1)CCCC(=O)OC)SC(=C2)CC ILKOIBBRSZNPGH-UHFFFAOYSA-N 0.000 description 1
- AEVBMPBKDYBNTN-UHFFFAOYSA-N methyl 4-[4-(1,3-benzodioxol-5-ylmethylamino)-6-methylthieno[2,3-d]pyrimidin-2-yl]butanoate methyl 4-(4-chloro-6-methylthieno[2,3-d]pyrimidin-2-yl)butanoate Chemical compound C1OC=2C=C(CNC=3C4=C(N=C(N3)CCCC(=O)OC)SC(=C4)C)C=CC2O1.ClC=1C2=C(N=C(N1)CCCC(=O)OC)SC(=C2)C AEVBMPBKDYBNTN-UHFFFAOYSA-N 0.000 description 1
- MVBAMFZRCDKPAL-UHFFFAOYSA-N methyl 4-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]butanoate Chemical compound C=12C=3CCCCC=3SC2=NC(CCCC(=O)OC)=NC=1NCC1=CC=C(OC)C(Cl)=C1 MVBAMFZRCDKPAL-UHFFFAOYSA-N 0.000 description 1
- GAOVHOGBMDDETD-UHFFFAOYSA-N methyl 5-(4-chloro-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)pentanoate Chemical compound COC(=O)CCCCC1=NC(Cl)=C2C(C)=C(C)SC2=N1 GAOVHOGBMDDETD-UHFFFAOYSA-N 0.000 description 1
- BLHNPKSMMWMNDJ-UHFFFAOYSA-N methyl 5-(4-chloro-6-ethylthieno[2,3-d]pyrimidin-2-yl)pentanoate Chemical compound N1=C(CCCCC(=O)OC)N=C2SC(CC)=CC2=C1Cl BLHNPKSMMWMNDJ-UHFFFAOYSA-N 0.000 description 1
- NGPLCBIPUVHOFO-UHFFFAOYSA-N methyl 5-(4-chloro-6-methylthieno[2,3-d]pyrimidin-2-yl)pentanoate Chemical compound COC(=O)CCCCC1=NC(Cl)=C2C=C(C)SC2=N1 NGPLCBIPUVHOFO-UHFFFAOYSA-N 0.000 description 1
- ZINZNVSMOGYBPJ-UHFFFAOYSA-N methyl 5-[4-(1,3-benzodioxol-5-ylmethylamino)-6-ethylthieno[2,3-d]pyrimidin-2-yl]pentanoate methyl 5-(4-chloro-6-ethylthieno[2,3-d]pyrimidin-2-yl)pentanoate Chemical compound CCc1cc2c(Cl)nc(CCCCC(=O)OC)nc2s1.CCc1cc2c(NCc3ccc4OCOc4c3)nc(CCCCC(=O)OC)nc2s1 ZINZNVSMOGYBPJ-UHFFFAOYSA-N 0.000 description 1
- LMMOVDDLRNRAAU-UHFFFAOYSA-N methyl 5-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]pentanoate Chemical compound C=12C=3CCCCC=3SC2=NC(CCCCC(=O)OC)=NC=1NCC1=CC=C(OC)C(Cl)=C1 LMMOVDDLRNRAAU-UHFFFAOYSA-N 0.000 description 1
- VEUSXDIAGUBKNA-UHFFFAOYSA-N methyl 7-(4-chloro-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl)heptanoate Chemical compound C1CCCC2=C1C1=C(Cl)N=C(CCCCCCC(=O)OC)N=C1S2 VEUSXDIAGUBKNA-UHFFFAOYSA-N 0.000 description 1
- SCLMBZDOVNJPBW-UHFFFAOYSA-N methyl 7-(4-chloro-6-methylthieno[2,3-d]pyrimidin-2-yl)heptanoate Chemical compound COC(=O)CCCCCCC1=NC(Cl)=C2C=C(C)SC2=N1 SCLMBZDOVNJPBW-UHFFFAOYSA-N 0.000 description 1
- VQAXSGZZZPGFCO-UHFFFAOYSA-N methyl 7-[4-(1,3-benzodioxol-5-ylmethylamino)-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl]heptanoate methyl 7-(4-chloro-5,6-dimethylthieno[2,3-d]pyrimidin-2-yl)heptanoate Chemical compound C1OC=2C=C(CNC=3C4=C(N=C(N3)CCCCCCC(=O)OC)SC(=C4C)C)C=CC2O1.ClC=1C2=C(N=C(N1)CCCCCCC(=O)OC)SC(=C2C)C VQAXSGZZZPGFCO-UHFFFAOYSA-N 0.000 description 1
- OCQARAQBGRNWQG-UHFFFAOYSA-N methyl 7-[4-(1,3-benzodioxol-5-ylmethylamino)-6-chlorothieno[2,3-d]pyrimidin-2-yl]heptanoate;methyl 7-(4,6-dichlorothieno[2,3-d]pyrimidin-2-yl)heptanoate Chemical compound COC(=O)CCCCCCC1=NC(Cl)=C2C=C(Cl)SC2=N1.C1=C2OCOC2=CC(CNC=2N=C(N=C3SC(Cl)=CC3=2)CCCCCCC(=O)OC)=C1 OCQARAQBGRNWQG-UHFFFAOYSA-N 0.000 description 1
- RRWKBLBUCIIZJL-UHFFFAOYSA-N methyl 7-[4-(1,3-benzodioxol-5-ylmethylamino)-6-ethylthieno[2,3-d]pyrimidin-2-yl]heptanoate;methyl 7-(4-chloro-6-ethylthieno[2,3-d]pyrimidin-2-yl)heptanoate Chemical compound N1=C(CCCCCCC(=O)OC)N=C2SC(CC)=CC2=C1Cl.C1=C2OCOC2=CC(CNC2=C3C=C(SC3=NC(CCCCCCC(=O)OC)=N2)CC)=C1 RRWKBLBUCIIZJL-UHFFFAOYSA-N 0.000 description 1
- RUDLKVBCNFDYAJ-UHFFFAOYSA-N methyl 7-[4-[(3-chloro-4-methoxyphenyl)methylamino]-5,6,7,8-tetrahydro-[1]benzothiolo[2,3-d]pyrimidin-2-yl]heptanoate Chemical compound C=12C=3CCCCC=3SC2=NC(CCCCCCC(=O)OC)=NC=1NCC1=CC=C(OC)C(Cl)=C1 RUDLKVBCNFDYAJ-UHFFFAOYSA-N 0.000 description 1
- UGESVNIAFODBKA-UHFFFAOYSA-N methyl 7-[6-chloro-4-[(3-chloro-4-methoxyphenyl)methylamino]thieno[2,3-d]pyrimidin-2-yl]heptanoate methyl 7-(4,6-dichlorothieno[2,3-d]pyrimidin-2-yl)heptanoate Chemical compound ClC=1C=C(CNC=2C3=C(N=C(N2)CCCCCCC(=O)OC)SC(=C3)Cl)C=CC1OC.ClC=1C3=C(N=C(N1)CCCCCCC(=O)OC)SC(=C3)Cl UGESVNIAFODBKA-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000036640 muscle relaxation Effects 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- BSCHIACBONPEOB-UHFFFAOYSA-N oxolane;hydrate Chemical compound O.C1CCOC1 BSCHIACBONPEOB-UHFFFAOYSA-N 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- SONNWYBIRXJNDC-VIFPVBQESA-N phenylephrine Chemical compound CNC[C@H](O)C1=CC=CC(O)=C1 SONNWYBIRXJNDC-VIFPVBQESA-N 0.000 description 1
- 229960001802 phenylephrine Drugs 0.000 description 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical class OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- DOTPSQVYOBAWPQ-UHFFFAOYSA-N pyrazolo[4,3-d]pyrimidin-3-one Chemical class N1=CN=C2C(=O)N=NC2=C1 DOTPSQVYOBAWPQ-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 150000003246 quinazolines Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000008347 soybean phospholipid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
-
- 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
-
- 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
- A61P9/02—Non-specific cardiovascular stimulants, e.g. drugs for syncope, antihypotensives
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Hospice & Palliative Care (AREA)
- Gynecology & Obstetrics (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (26)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752952A DE19752952A1 (de) | 1997-11-28 | 1997-11-28 | Thienopyrimidine |
| DE59814003T DE59814003D1 (en) | 1997-11-28 | 1998-11-19 | Thienopyrimidine |
| CNB988113767A CN1138780C (zh) | 1997-11-28 | 1998-11-19 | 噻吩并嘧啶类 |
| US09/555,210 US6420368B1 (en) | 1997-11-28 | 1998-11-19 | Thienopyrimidines |
| EP98964411A EP1036078B1 (de) | 1997-11-28 | 1998-11-19 | Thienopyrimidine |
| CA002311922A CA2311922C (en) | 1997-11-28 | 1998-11-19 | Thienopyrimidines |
| AU19625/99A AU742433B2 (en) | 1997-11-28 | 1998-11-19 | Thienopyrimidines |
| JP2000523217A JP4314341B2 (ja) | 1997-11-28 | 1998-11-19 | チエノピリミジン類 |
| HK02100600.0A HK1038924A1 (zh) | 1997-11-28 | 1998-11-19 | 噻吩並嘧啶類 |
| IDW20000942A ID24571A (id) | 1997-11-28 | 1998-11-19 | Senyawa tienopirimidin |
| KR1020007005686A KR20010032445A (ko) | 1997-11-28 | 1998-11-19 | 티에노피리미딘 |
| RU2000116899/04A RU2217431C2 (ru) | 1997-11-28 | 1998-11-19 | Тиенопиримидины, способ их получения, фармацевтическая композиция, обладающая действием ингибиторов фосфодиэстеразы v |
| PL98341156A PL341156A1 (en) | 1997-11-28 | 1998-11-19 | Thienopyrimidines |
| HU0100488A HUP0100488A3 (en) | 1997-11-28 | 1998-11-19 | Thienopyrimidines, process for their preparation and pharmaceutical compositions containing them |
| BR9815409-5A BR9815409A (pt) | 1997-11-28 | 1998-11-19 | Tienopirimidinas |
| SK777-2000A SK7772000A3 (en) | 1997-11-28 | 1998-11-19 | Thienopyrimidine derivative, process for the preparation thereof, use thereof and pharmaceutical composition containing same |
| ES98964411T ES2285796T3 (es) | 1997-11-28 | 1998-11-19 | Tienopirimidinas. |
| CZ20001962A CZ291068B6 (cs) | 1997-11-28 | 1998-11-19 | Derivát thienopyrimidinu, způsob jeho přípravy, jeho pouľití a farmaceutický prostředek, který ho obsahuje |
| AT98964411T ATE361926T1 (de) | 1997-11-28 | 1998-11-19 | Thienopyrimidine |
| PCT/EP1998/007436 WO1999028325A1 (de) | 1997-11-28 | 1998-11-19 | Thienopyrimidine |
| TW087119650A TW472059B (en) | 1997-11-28 | 1998-11-26 | Thienopyrimidines, preparation process thereof, and pharmaceutical composition containing the same |
| ZA9810845A ZA9810845B (en) | 1997-11-28 | 1998-11-26 | Thienopyrimidines |
| ARP980106028A AR010962A1 (es) | 1997-11-28 | 1998-11-27 | Tienopirimidinas, un procedimiento para su preparacion, empleo de las mismas para preparar un medicamento, preparaciones farmaceuticas que lascontienen, y un procedimiento para obtener estas preparaciones farmaceuticas. |
| CO98070308A CO4980884A1 (es) | 1997-11-28 | 1998-11-27 | Tienopirimidinas |
| NO20002702A NO20002702D0 (no) | 1997-11-28 | 2000-05-26 | Tienopyrimidiner |
| US10/146,028 US6495554B2 (en) | 1997-11-28 | 2002-05-16 | Thienopyrimidines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752952A DE19752952A1 (de) | 1997-11-28 | 1997-11-28 | Thienopyrimidine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE19752952A1 true DE19752952A1 (de) | 1999-06-02 |
Family
ID=7850200
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19752952A Withdrawn DE19752952A1 (de) | 1997-11-28 | 1997-11-28 | Thienopyrimidine |
| DE59814003T Expired - Lifetime DE59814003D1 (en) | 1997-11-28 | 1998-11-19 | Thienopyrimidine |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE59814003T Expired - Lifetime DE59814003D1 (en) | 1997-11-28 | 1998-11-19 | Thienopyrimidine |
Country Status (24)
| Country | Link |
|---|---|
| US (2) | US6420368B1 (enExample) |
| EP (1) | EP1036078B1 (enExample) |
| JP (1) | JP4314341B2 (enExample) |
| KR (1) | KR20010032445A (enExample) |
| CN (1) | CN1138780C (enExample) |
| AR (1) | AR010962A1 (enExample) |
| AT (1) | ATE361926T1 (enExample) |
| AU (1) | AU742433B2 (enExample) |
| BR (1) | BR9815409A (enExample) |
| CA (1) | CA2311922C (enExample) |
| CO (1) | CO4980884A1 (enExample) |
| CZ (1) | CZ291068B6 (enExample) |
| DE (2) | DE19752952A1 (enExample) |
| ES (1) | ES2285796T3 (enExample) |
| HK (1) | HK1038924A1 (enExample) |
| HU (1) | HUP0100488A3 (enExample) |
| ID (1) | ID24571A (enExample) |
| NO (1) | NO20002702D0 (enExample) |
| PL (1) | PL341156A1 (enExample) |
| RU (1) | RU2217431C2 (enExample) |
| SK (1) | SK7772000A3 (enExample) |
| TW (1) | TW472059B (enExample) |
| WO (1) | WO1999028325A1 (enExample) |
| ZA (1) | ZA9810845B (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002059126A1 (en) * | 2001-01-27 | 2002-08-01 | Merck Patent Gmbh | Process for the preparation of a pyrazolo[4,3-d]pyrimidine derivative |
| WO2002018389A3 (de) * | 2000-09-01 | 2003-07-03 | Merck Patent Gmbh | Thienopyrimidine |
| RU2261863C2 (ru) * | 2000-06-29 | 2005-10-10 | Мерк Патент Гмбх | 2-аминоалкилтиено[2,3-d]пиримидины, способ их получения, лекарственный препарат и способ его получения |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19819023A1 (de) | 1998-04-29 | 1999-11-04 | Merck Patent Gmbh | Thienopyrimidine |
| CA2365578A1 (en) | 1999-03-30 | 2000-10-12 | Seiichi Uchida | Thienopyrimidine compounds and salts thereof and process for the preparation of the same |
| DE19942474A1 (de) * | 1999-09-06 | 2001-03-15 | Merck Patent Gmbh | Pyrazolo[4,3-d]pyrimidine |
| CN1436080A (zh) | 2000-04-19 | 2003-08-13 | 利利艾科斯有限公司 | 环gmp－特异性磷酸二酯酶抑制剂治疗帕金森氏病的用途 |
| DE10031584A1 (de) | 2000-06-29 | 2002-01-10 | Merck Patent Gmbh | 5-Aminoalkyl-pyrazolo[4,3-d]pyrimidine |
| CA2423981A1 (en) * | 2000-09-29 | 2003-03-28 | Kimiko Ichikawa | Thienopyrimidine compounds and salts thereof and process for the preparation of the same |
| DE10058663A1 (de) * | 2000-11-25 | 2002-05-29 | Merck Patent Gmbh | Verwendung von Thienopyrimidinen |
| AU2002227957A1 (en) * | 2000-12-19 | 2002-07-01 | Merck Patent Gmbh | Pharmaceutical formulation containing thienopyrimidines and antithrombotics, calcium antagonists, prostaglandins or prostaglandin derivatives |
| DE10064994A1 (de) * | 2000-12-23 | 2002-07-04 | Merck Patent Gmbh | Sulfamidothienopyrimidine |
| WO2002060449A2 (de) * | 2001-01-31 | 2002-08-08 | Merck Patent Gmbh | Pharmazeutische formulierung enthaltend pyrazolo[4,3-d]pyrimidine und nitrate oder thienopyrimidine und nitrate |
| CN101100472A (zh) * | 2001-04-30 | 2008-01-09 | 美国拜尔公司 | 4-氨基-5,6-取代的噻吩并[2,3-d]嘧啶化合物及其应用 |
| DE10148883A1 (de) * | 2001-10-04 | 2003-04-10 | Merck Patent Gmbh | Pyrimidinderivate |
| JPWO2003035653A1 (ja) * | 2001-10-26 | 2005-02-10 | 日本曹達株式会社 | ピリドチエノピリミジン化合物およびその塩 |
| KR100824193B1 (ko) | 2003-04-29 | 2008-04-21 | 화이자 인코포레이티드 | 고혈압 치료에 유용한5,7-디아미노피라졸로[4,3-ｄ]피리미딘 |
| US7572799B2 (en) | 2003-11-24 | 2009-08-11 | Pfizer Inc | Pyrazolo[4,3-d]pyrimidines as Phosphodiesterase Inhibitors |
| JP2007532526A (ja) | 2004-04-07 | 2007-11-15 | ファイザー・インク | ピラゾロ［４，３−ｄ］ピリミジン類 |
| GB0420719D0 (en) * | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| ES2259891B1 (es) * | 2004-11-30 | 2007-11-01 | Laboratorios Almirall S.A. | Nuevos derivados de piridotienopirimidina. |
| ES2259892B1 (es) * | 2004-11-30 | 2007-11-01 | Laboratorios Almirall S.A. | Nuevos derivados de piridotienopirimidina. |
| US9056877B2 (en) | 2011-07-19 | 2015-06-16 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| CN109297923A (zh) * | 2018-09-19 | 2019-02-01 | 南通出入境检验检疫局检验检疫综合技术中心 | 纺织品中微量含氟整理剂的测定方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE245666C (enExample) | ||||
| DD245666A1 (de) * | 1985-09-20 | 1987-05-13 | Univ Halle Wittenberg | Verfahren zur herstellung von 4-aminosubstituierten thieno 2,3-d-pyrimidin-2-ylessigsaeureestern |
| GB9301192D0 (en) * | 1993-06-09 | 1993-06-09 | Trott Francis W | Flower shaped mechanised table |
| US5869486A (en) * | 1995-02-24 | 1999-02-09 | Ono Pharmaceutical Co., Ltd. | Fused pyrimidines and pyriazines as pharmaceutical compounds |
| DE19644228A1 (de) | 1996-10-24 | 1998-04-30 | Merck Patent Gmbh | Thienopyrimidine |
-
1997
- 1997-11-28 DE DE19752952A patent/DE19752952A1/de not_active Withdrawn
-
1998
- 1998-11-19 HK HK02100600.0A patent/HK1038924A1/zh unknown
- 1998-11-19 AT AT98964411T patent/ATE361926T1/de not_active IP Right Cessation
- 1998-11-19 KR KR1020007005686A patent/KR20010032445A/ko not_active Abandoned
- 1998-11-19 CN CNB988113767A patent/CN1138780C/zh not_active Expired - Fee Related
- 1998-11-19 PL PL98341156A patent/PL341156A1/xx not_active Application Discontinuation
- 1998-11-19 HU HU0100488A patent/HUP0100488A3/hu unknown
- 1998-11-19 BR BR9815409-5A patent/BR9815409A/pt not_active Application Discontinuation
- 1998-11-19 WO PCT/EP1998/007436 patent/WO1999028325A1/de not_active Ceased
- 1998-11-19 ES ES98964411T patent/ES2285796T3/es not_active Expired - Lifetime
- 1998-11-19 US US09/555,210 patent/US6420368B1/en not_active Expired - Fee Related
- 1998-11-19 EP EP98964411A patent/EP1036078B1/de not_active Expired - Lifetime
- 1998-11-19 CZ CZ20001962A patent/CZ291068B6/cs not_active IP Right Cessation
- 1998-11-19 ID IDW20000942A patent/ID24571A/id unknown
- 1998-11-19 JP JP2000523217A patent/JP4314341B2/ja not_active Expired - Fee Related
- 1998-11-19 AU AU19625/99A patent/AU742433B2/en not_active Ceased
- 1998-11-19 SK SK777-2000A patent/SK7772000A3/sk unknown
- 1998-11-19 RU RU2000116899/04A patent/RU2217431C2/ru not_active IP Right Cessation
- 1998-11-19 DE DE59814003T patent/DE59814003D1/de not_active Expired - Lifetime
- 1998-11-19 CA CA002311922A patent/CA2311922C/en not_active Expired - Fee Related
- 1998-11-26 TW TW087119650A patent/TW472059B/zh not_active IP Right Cessation
- 1998-11-26 ZA ZA9810845A patent/ZA9810845B/xx unknown
- 1998-11-27 CO CO98070308A patent/CO4980884A1/es unknown
- 1998-11-27 AR ARP980106028A patent/AR010962A1/es not_active Application Discontinuation
-
2000
- 2000-05-26 NO NO20002702A patent/NO20002702D0/no not_active Application Discontinuation
-
2002
- 2002-05-16 US US10/146,028 patent/US6495554B2/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2261863C2 (ru) * | 2000-06-29 | 2005-10-10 | Мерк Патент Гмбх | 2-аминоалкилтиено[2,3-d]пиримидины, способ их получения, лекарственный препарат и способ его получения |
| WO2002018389A3 (de) * | 2000-09-01 | 2003-07-03 | Merck Patent Gmbh | Thienopyrimidine |
| US6780867B2 (en) * | 2000-09-01 | 2004-08-24 | Merck Patent Gmbh | Thienopyrimidines |
| WO2002059126A1 (en) * | 2001-01-27 | 2002-08-01 | Merck Patent Gmbh | Process for the preparation of a pyrazolo[4,3-d]pyrimidine derivative |
| US6960661B2 (en) | 2001-01-27 | 2005-11-01 | Merck Patent Gmbh | [7-(3-chloro-4-methoxybenzlamino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-5-ylmethoxy]acetic acid, synthesis thereof and intermediates used therein |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2311922C (en) | 2009-09-29 |
| JP4314341B2 (ja) | 2009-08-12 |
| CZ20001962A3 (cs) | 2002-01-16 |
| HUP0100488A3 (en) | 2003-03-28 |
| EP1036078A1 (de) | 2000-09-20 |
| AU742433B2 (en) | 2002-01-03 |
| DE59814003D1 (en) | 2007-06-21 |
| PL341156A1 (en) | 2001-03-26 |
| CA2311922A1 (en) | 1999-06-10 |
| CZ291068B6 (cs) | 2002-12-11 |
| EP1036078B1 (de) | 2007-05-09 |
| TW472059B (en) | 2002-01-11 |
| CO4980884A1 (es) | 2000-11-27 |
| SK7772000A3 (en) | 2000-12-11 |
| US6495554B2 (en) | 2002-12-17 |
| AU1962599A (en) | 1999-06-16 |
| RU2217431C2 (ru) | 2003-11-27 |
| NO20002702L (no) | 2000-05-26 |
| ES2285796T3 (es) | 2007-11-16 |
| HUP0100488A2 (hu) | 2001-09-28 |
| US6420368B1 (en) | 2002-07-16 |
| HK1038924A1 (zh) | 2002-04-04 |
| WO1999028325A1 (de) | 1999-06-10 |
| BR9815409A (pt) | 2000-10-24 |
| JP2001525325A (ja) | 2001-12-11 |
| ZA9810845B (en) | 1999-05-26 |
| KR20010032445A (ko) | 2001-04-25 |
| US20020132818A1 (en) | 2002-09-19 |
| CN1306534A (zh) | 2001-08-01 |
| ATE361926T1 (de) | 2007-06-15 |
| ID24571A (id) | 2000-07-27 |
| CN1138780C (zh) | 2004-02-18 |
| NO20002702D0 (no) | 2000-05-26 |
| AR010962A1 (es) | 2000-07-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1036078B1 (de) | Thienopyrimidine | |
| DE19644228A1 (de) | Thienopyrimidine | |
| DE10058663A1 (de) | Verwendung von Thienopyrimidinen | |
| EP1189907B1 (de) | Thienopyrimidine als phosphodiesterase hemmer | |
| EP1084125B1 (de) | Kondensierte thienopyrimidine mit pde v inhibierender wirkung | |
| EP1210349B1 (de) | Pyrazolo[4, 3-d]pyrimidine | |
| DE10064994A1 (de) | Sulfamidothienopyrimidine | |
| DE10058662A1 (de) | Verwendung von Pyrazolo[4,3-d]pyrimidinen | |
| EP1355649A2 (de) | Pharmazeutische formulierung enthaltend pyrazolo 4,3-d]pyrimidine und nitrate oder thienopyrimidine und nitrate | |
| DE10060388A1 (de) | Verwendung von Pyrazolo [4,3-d]pyrimidinen | |
| DE10104802A1 (de) | Pharmazeutische Formulierungen enthaltend Thienopirimidine und Endothelin-Rezeptor-Antagonisten (1) | |
| DE10010612A1 (de) | Verwendung von PDE V-Inhibitoren | |
| EP1351962B1 (de) | Thienopyrimidine | |
| DE19943815A1 (de) | Verwendung von Thienopyrimidinen | |
| DE19944604A1 (de) | Aminderivate | |
| DE10104097A1 (de) | Pharmazeutische Formulierung enthaltend Thienopyrimidine und Nitrate | |
| DE10104096A1 (de) | Pharmazeutische Formulierung enthaltend Thienopyrimidine und Nitrate | |
| DE10064991A1 (de) | Pharmazeutische Formulierung enthaltend Thienopyrimidine und Prostaglandine oder Prostaglandinderivate (2) | |
| DE10104095A1 (de) | Pharmazeutische Formulierung enthaltend Pyrazolo [4,3-d]pyrimidine und Nitrate | |
| DE10064992A1 (de) | Pharmazeutische Formulierung enthaltend Thienopyrimidine und Prostaglandine oder Prostaglandinderivate (1) | |
| DE10104801A1 (de) | Pharmazeutische Formulierungen enthaltend Thienopirimidine und Endothelin-Rezeptor-Antagonisten (2) | |
| DE10063885A1 (de) | Pharmazeutische Formulierung enthaltend Thienopyrimidine und Calcium-Antagonisten (1) | |
| DE10063884A1 (de) | Pharmazeutische Formulierung enthaltend Thienopyrimidine und Calcium-Antagonisten (2) | |
| DE10064993A1 (de) | Pharmazeutische Formulierung enthaltend Pyrazolo[4,3-d]pyrimidine und Prostaglandine oder Prostaglandinderivate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8139 | Disposal/non-payment of the annual fee |