SE436883B - Pyrimido /1,2-a/ azepinderivat, forfarande for deras framstellning och farmaceutiskt preparat - Google Patents
Pyrimido /1,2-a/ azepinderivat, forfarande for deras framstellning och farmaceutiskt preparatInfo
- Publication number
- SE436883B SE436883B SE8003478A SE8003478A SE436883B SE 436883 B SE436883 B SE 436883B SE 8003478 A SE8003478 A SE 8003478A SE 8003478 A SE8003478 A SE 8003478A SE 436883 B SE436883 B SE 436883B
- Authority
- SE
- Sweden
- Prior art keywords
- lower alkyl
- general formula
- pyrimido
- hydrogen
- compound
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 8
- 239000000825 pharmaceutical preparation Substances 0.000 title claims description 3
- 150000001538 azepines Chemical class 0.000 title claims 2
- 238000002360 preparation method Methods 0.000 title description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 59
- 150000001875 compounds Chemical class 0.000 claims description 36
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 claims description 23
- 239000000203 mixture Substances 0.000 claims description 19
- 150000003839 salts Chemical class 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 15
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- XEVRDFDBXJMZFG-UHFFFAOYSA-N carbonyl dihydrazine Chemical compound NNC(=O)NN XEVRDFDBXJMZFG-UHFFFAOYSA-N 0.000 claims description 8
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 150000002825 nitriles Chemical class 0.000 claims description 6
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- GTLJSJNKRLFVSJ-UHFFFAOYSA-N 3,4,5,6-tetrahydro-2h-azepin-7-amine Chemical class N=C1CCCCCN1 GTLJSJNKRLFVSJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 3
- 230000003257 anti-anginal effect Effects 0.000 claims description 3
- LTMHNWPUDSTBKD-UHFFFAOYSA-N diethyl 2-(ethoxymethylidene)propanedioate Chemical compound CCOC=C(C(=O)OCC)C(=O)OCC LTMHNWPUDSTBKD-UHFFFAOYSA-N 0.000 claims description 3
- OKANYBNORCUPKZ-UHFFFAOYSA-N ethyl 2-ethyl-3-oxobutanoate Chemical compound CCOC(=O)C(CC)C(C)=O OKANYBNORCUPKZ-UHFFFAOYSA-N 0.000 claims description 3
- GWMGLJWGCQLFBK-UHFFFAOYSA-N 1h-pyrimido[1,2-a]azepin-2-one Chemical compound C1=CC=CN2C=CC(=O)NC2=C1 GWMGLJWGCQLFBK-UHFFFAOYSA-N 0.000 claims description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
- XWIUIRQSQROZGJ-UHFFFAOYSA-N ethyl 2-(2-formylphenyl)acetate Chemical compound CCOC(=O)CC1=CC=CC=C1C=O XWIUIRQSQROZGJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000012442 inert solvent Substances 0.000 claims description 2
- TWFWQBPKFXUCJF-UHFFFAOYSA-N 3h-pyrimido[1,2-a]azepin-4-one Chemical compound C1=CC=CN2C(=O)CC=NC2=C1 TWFWQBPKFXUCJF-UHFFFAOYSA-N 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 238000001640 fractional crystallisation Methods 0.000 claims 1
- 238000007127 saponification reaction Methods 0.000 claims 1
- 239000000243 solution Substances 0.000 description 31
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 27
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 27
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- 230000008018 melting Effects 0.000 description 11
- 238000002844 melting Methods 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 239000013078 crystal Substances 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- BATMIEQLHWRSOU-UHFFFAOYSA-N ethyl 2-oxo-7,8,9,10-tetrahydro-6h-pyrimido[1,2-a]azepine-3-carboxylate Chemical compound C1CCCCC2=NC(=O)C(C(=O)OCC)=CN21 BATMIEQLHWRSOU-UHFFFAOYSA-N 0.000 description 5
- FVZLXIARAAOVCZ-UHFFFAOYSA-N 1h-azepine-3-carboxylic acid Chemical compound OC(=O)C1=CNC=CC=C1 FVZLXIARAAOVCZ-UHFFFAOYSA-N 0.000 description 4
- 229960001701 chloroform Drugs 0.000 description 4
- 125000004093 cyano group Chemical group *C#N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 description 3
- 150000003857 carboxamides Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000004185 ester group Chemical group 0.000 description 3
- MYFDRUDDHLKXHE-UHFFFAOYSA-N ethyl 4-oxo-7,8,9,10-tetrahydro-6h-pyrimido[1,2-a]azepine-3-carboxylate Chemical compound C1CCCCN2C(=O)C(C(=O)OCC)=CN=C21 MYFDRUDDHLKXHE-UHFFFAOYSA-N 0.000 description 3
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- -1 robromide Chemical compound 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- LEUMFSTVJGBXTL-UHFFFAOYSA-N 3-phenyl-7,8,9,10-tetrahydro-6h-pyrimido[1,2-a]azepin-4-one Chemical compound C=1N=C2CCCCCN2C(=O)C=1C1=CC=CC=C1 LEUMFSTVJGBXTL-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- XQYZDYMELSJDRZ-UHFFFAOYSA-N papaverine Chemical compound C1=C(OC)C(OC)=CC=C1CC1=NC=CC2=CC(OC)=C(OC)C=C12 XQYZDYMELSJDRZ-UHFFFAOYSA-N 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000010453 quartz Chemical class 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- OBTZDIRUQWFRFZ-UHFFFAOYSA-N 2-(5-methylfuran-2-yl)-n-(4-methylphenyl)quinoline-4-carboxamide Chemical compound O1C(C)=CC=C1C1=CC(C(=O)NC=2C=CC(C)=CC=2)=C(C=CC=C2)C2=N1 OBTZDIRUQWFRFZ-UHFFFAOYSA-N 0.000 description 1
- AVAQZFUVMGMHSC-UHFFFAOYSA-N 2-cyano-3-ethoxyprop-2-enoic acid Chemical compound CCOC=C(C#N)C(O)=O AVAQZFUVMGMHSC-UHFFFAOYSA-N 0.000 description 1
- DERAACKMMNJAFU-UHFFFAOYSA-N 2-ethoxy-1,3-dioxane-4,6-dione Chemical compound CCOC1OC(=O)CC(=O)O1 DERAACKMMNJAFU-UHFFFAOYSA-N 0.000 description 1
- VXJCASDXQBLRNI-UHFFFAOYSA-N 2-ethyl-7,8,9,10-tetrahydro-6H-pyrimido[1,2-a]azepin-4-one Chemical compound C(C)C=1N=C2N(CCCCC2)C(C1)=O VXJCASDXQBLRNI-UHFFFAOYSA-N 0.000 description 1
- OPIOZHYBAWFMHX-UHFFFAOYSA-N 2-oxo-7,8,9,10-tetrahydro-6H-pyrimido[1,2-a]azepine-3-carbohydrazide Chemical compound O=C1N=C2N(CCCCC2)C=C1C(=O)NN OPIOZHYBAWFMHX-UHFFFAOYSA-N 0.000 description 1
- UHXGKJKOBGPMIE-UHFFFAOYSA-N 2-oxo-7,8,9,10-tetrahydro-6h-pyrimido[1,2-a]azepine-3-carbonitrile Chemical compound C1CCCCN2C=C(C#N)C(=O)N=C21 UHXGKJKOBGPMIE-UHFFFAOYSA-N 0.000 description 1
- SOAWFTPUJKSXDC-UHFFFAOYSA-N 2-oxo-7,8,9,10-tetrahydro-6h-pyrimido[1,2-a]azepine-3-carboxylic acid Chemical compound C1CCCCC2=NC(=O)C(C(=O)O)=CN21 SOAWFTPUJKSXDC-UHFFFAOYSA-N 0.000 description 1
- ADLRXOVAMNULLA-UHFFFAOYSA-N 3,4,5,6-tetrahydro-2h-azepin-2-amine Chemical compound NC1CCCCC=N1 ADLRXOVAMNULLA-UHFFFAOYSA-N 0.000 description 1
- ZPDCGNJMYKAWOB-UHFFFAOYSA-N 3-ethyl-2-methyl-7,8,9,10-tetrahydro-6h-pyrimido[1,2-a]azepin-4-one Chemical compound C1CCCCN2C(=O)C(CC)=C(C)N=C21 ZPDCGNJMYKAWOB-UHFFFAOYSA-N 0.000 description 1
- KJIYVLIKLRBGBU-UHFFFAOYSA-N 3-methyl-7,8,9,10-tetrahydro-6h-pyrimido[1,2-a]azepin-4-one;hydrochloride Chemical compound Cl.C1CCCCN2C(=O)C(C)=CN=C21 KJIYVLIKLRBGBU-UHFFFAOYSA-N 0.000 description 1
- WURIPXVKHXQECZ-UHFFFAOYSA-N 3-phenyl-7,8,9,10-tetrahydro-6h-pyrimido[1,2-a]azepin-2-one Chemical compound O=C1N=C2CCCCCN2C=C1C1=CC=CC=C1 WURIPXVKHXQECZ-UHFFFAOYSA-N 0.000 description 1
- IRIDIPVOTWFODI-UHFFFAOYSA-N 4-oxo-7,8,9,10-tetrahydro-6h-pyrimido[1,2-a]azepine-3-carbonitrile Chemical compound C1CCCCN2C(=O)C(C#N)=CN=C21 IRIDIPVOTWFODI-UHFFFAOYSA-N 0.000 description 1
- COWHMHWSHQPEAB-UHFFFAOYSA-N 7-methyl-3,4,5,6-tetrahydro-2h-azepin-2-amine Chemical compound CC1=NC(N)CCCC1 COWHMHWSHQPEAB-UHFFFAOYSA-N 0.000 description 1
- 229930008281 A03AD01 - Papaverine Natural products 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 206010052895 Coronary artery insufficiency Diseases 0.000 description 1
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 description 1
- FFGASZNXDRJHAV-UHFFFAOYSA-N S(=O)(=O)(OC)[O-].[NH2+]1C=CC=CC=C1 Chemical compound S(=O)(=O)(OC)[O-].[NH2+]1C=CC=CC=C1 FFGASZNXDRJHAV-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- WLXALCKAKGDNAT-UHFFFAOYSA-N diazoethane Chemical compound CC=[N+]=[N-] WLXALCKAKGDNAT-UHFFFAOYSA-N 0.000 description 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
- KTMGNAIGXYODKQ-UHFFFAOYSA-N ethyl 2-cyano-3-ethoxyprop-2-enoate Chemical compound CCOC=C(C#N)C(=O)OCC KTMGNAIGXYODKQ-UHFFFAOYSA-N 0.000 description 1
- VVCYNVCCODBCOE-UHFFFAOYSA-N ethyl 2-methyl-3-oxopropanoate Chemical compound CCOC(=O)C(C)C=O VVCYNVCCODBCOE-UHFFFAOYSA-N 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 229940052308 general anesthetics halogenated hydrocarbons Drugs 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 150000002500 ions Chemical class 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
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 229960001789 papaverine Drugs 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 210000004197 pelvis Anatomy 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Heart & Thoracic Surgery (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU79CI1931A HU177184B (en) | 1979-05-11 | 1979-05-11 | Process for producing 2,3- and 3,4-disubstituted-hexahydro-pyrimido-square bracket-1,2-a-square bracket closed-asepines |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE8003478L SE8003478L (sv) | 1980-11-12 |
| SE436883B true SE436883B (sv) | 1985-01-28 |
Family
ID=10994746
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8003478A SE436883B (sv) | 1979-05-11 | 1980-05-08 | Pyrimido /1,2-a/ azepinderivat, forfarande for deras framstellning och farmaceutiskt preparat |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US4404205A (pl) |
| JP (1) | JPS5618984A (pl) |
| AR (1) | AR228136A1 (pl) |
| AT (1) | AT390615B (pl) |
| AU (1) | AU541505B2 (pl) |
| BE (1) | BE883216A (pl) |
| CA (1) | CA1143729A (pl) |
| CH (1) | CH649552A5 (pl) |
| CS (1) | CS216529B2 (pl) |
| DD (1) | DD150611A5 (pl) |
| DE (1) | DE3017565A1 (pl) |
| DK (1) | DK152500C (pl) |
| ES (1) | ES491360A0 (pl) |
| FI (1) | FI70217C (pl) |
| FR (2) | FR2456106A1 (pl) |
| GB (1) | GB2051047B (pl) |
| GR (1) | GR68520B (pl) |
| HU (1) | HU177184B (pl) |
| IL (1) | IL60026A (pl) |
| IT (1) | IT1147733B (pl) |
| LU (1) | LU82436A1 (pl) |
| NL (1) | NL8002683A (pl) |
| NO (1) | NO154427C (pl) |
| PL (1) | PL123691B1 (pl) |
| PT (1) | PT71212A (pl) |
| SE (1) | SE436883B (pl) |
| SU (1) | SU981319A1 (pl) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU191192B (en) * | 1982-11-16 | 1987-01-28 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu | Process for producing new azepino /1,2-a/ pyrimidine derivatives of bronchodilating activity and acid additional salts thereof and pharmaceiutical compositions containing them |
| US11681227B2 (en) * | 2019-02-25 | 2023-06-20 | Alex P. G. Robinson | Enhanced EUV photoresist materials, formulations and processes |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE451733C (de) | 1923-07-21 | 1927-11-03 | A E Tschitschibabin Dr | Verfahren zur Darstellung von dicyklischen und polycyklischen Verbindungen, die hydrierte oder nichthydrierte Imidazol- oder Pyrimidinkerne enthalten |
| US3002000A (en) * | 1958-11-08 | 1961-09-26 | Bayer Ag | 1,2-alkylene-dihydropyrimidone-6, and 1,2-alkylene-imidazolinones-(5) |
| AT286990B (de) * | 1966-11-02 | 1971-01-11 | Chinoin Gyogyszer Es Vegyeszet | Verfahren zur Herstellung von neuen Homopyrimidazol-Derivaten sowie von deren Salzen |
| BE788601A (fr) | 1971-09-10 | 1973-03-08 | Takeda Chemical Industries Ltd | Procede de preparation de derives de pyrimidine |
| HU167676B (pl) * | 1972-11-29 | 1975-11-28 |
-
1979
- 1979-05-11 HU HU79CI1931A patent/HU177184B/hu not_active IP Right Cessation
-
1980
- 1980-05-03 GR GR61854A patent/GR68520B/el unknown
- 1980-05-08 SE SE8003478A patent/SE436883B/sv not_active IP Right Cessation
- 1980-05-08 DE DE19803017565 patent/DE3017565A1/de not_active Withdrawn
- 1980-05-08 CS CS803260A patent/CS216529B2/cs unknown
- 1980-05-08 IL IL60026A patent/IL60026A/xx unknown
- 1980-05-08 SU SU802921150A patent/SU981319A1/ru active
- 1980-05-09 LU LU82436A patent/LU82436A1/de unknown
- 1980-05-09 BE BE0/200549A patent/BE883216A/fr not_active IP Right Cessation
- 1980-05-09 NO NO801377A patent/NO154427C/no unknown
- 1980-05-09 GB GB8015418A patent/GB2051047B/en not_active Expired
- 1980-05-09 AR AR280968A patent/AR228136A1/es active
- 1980-05-09 CH CH3662/80A patent/CH649552A5/de not_active IP Right Cessation
- 1980-05-09 JP JP6161580A patent/JPS5618984A/ja active Pending
- 1980-05-09 IT IT67722/80A patent/IT1147733B/it active
- 1980-05-09 AU AU58277/80A patent/AU541505B2/en not_active Ceased
- 1980-05-09 DD DD80220985A patent/DD150611A5/de not_active IP Right Cessation
- 1980-05-09 FI FI801514A patent/FI70217C/fi not_active IP Right Cessation
- 1980-05-09 AT AT0247380A patent/AT390615B/de not_active IP Right Cessation
- 1980-05-09 US US06/148,234 patent/US4404205A/en not_active Expired - Lifetime
- 1980-05-09 FR FR8010479A patent/FR2456106A1/fr active Granted
- 1980-05-09 ES ES491360A patent/ES491360A0/es active Granted
- 1980-05-09 NL NL8002683A patent/NL8002683A/nl not_active Application Discontinuation
- 1980-05-09 PT PT71212A patent/PT71212A/pt unknown
- 1980-05-09 CA CA000351665A patent/CA1143729A/en not_active Expired
- 1980-05-09 DK DK204780A patent/DK152500C/da not_active IP Right Cessation
- 1980-05-10 PL PL1980224165A patent/PL123691B1/pl unknown
-
1981
- 1981-04-08 FR FR8107052A patent/FR2480602A1/fr active Granted
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Legal Events
| Date | Code | Title | Description |
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| NUG | Patent has lapsed |
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