KR100628676B1 - 카바페넴 화합물의 제조방법 - Google Patents
카바페넴 화합물의 제조방법 Download PDFInfo
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- KR100628676B1 KR100628676B1 KR1020047004533A KR20047004533A KR100628676B1 KR 100628676 B1 KR100628676 B1 KR 100628676B1 KR 1020047004533 A KR1020047004533 A KR 1020047004533A KR 20047004533 A KR20047004533 A KR 20047004533A KR 100628676 B1 KR100628676 B1 KR 100628676B1
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- organic solvent
- formula
- solid
- propanol
- crystalline carbapenem
- Prior art date
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- YZBQHRLRFGPBSL-RXMQYKEDSA-N carbapenem Chemical class C1C=CN2C(=O)C[C@H]21 YZBQHRLRFGPBSL-RXMQYKEDSA-N 0.000 title claims abstract description 66
- 238000000034 method Methods 0.000 title claims abstract description 55
- 239000007787 solid Substances 0.000 claims abstract description 107
- 239000003960 organic solvent Substances 0.000 claims abstract description 105
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 77
- 150000001875 compounds Chemical class 0.000 claims abstract description 54
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 31
- 239000011261 inert gas Substances 0.000 claims abstract description 30
- 125000003118 aryl group Chemical group 0.000 claims abstract description 19
- 150000003839 salts Chemical class 0.000 claims abstract description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 81
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 81
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 72
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 65
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 51
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 49
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 40
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 40
- 239000000203 mixture Substances 0.000 claims description 33
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 30
- 229910052757 nitrogen Inorganic materials 0.000 claims description 26
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 20
- 238000000634 powder X-ray diffraction Methods 0.000 claims description 20
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 18
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 17
- 238000005406 washing Methods 0.000 claims description 16
- -1 aralkoxy Chemical group 0.000 claims description 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 13
- 238000001704 evaporation Methods 0.000 claims description 12
- 238000004458 analytical method Methods 0.000 claims description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 10
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 9
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 7
- 238000004140 cleaning Methods 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 claims description 6
- 229940011051 isopropyl acetate Drugs 0.000 claims description 6
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 230000008020 evaporation Effects 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 5
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 125000004442 acylamino group Chemical group 0.000 claims description 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 3
- 125000003282 alkyl amino group Chemical group 0.000 claims description 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 3
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims description 3
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 3
- 125000004104 aryloxy group Chemical group 0.000 claims description 3
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 3
- 150000002825 nitriles Chemical class 0.000 claims description 3
- 239000013557 residual solvent Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 claims description 3
- 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 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 229910001873 dinitrogen Inorganic materials 0.000 claims 1
- DJNNIRDYGMGYHD-UHFFFAOYSA-M sodium 4-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate Chemical compound [Na+].O=C1C=C(N2CCC12)C(=O)[O-] DJNNIRDYGMGYHD-UHFFFAOYSA-M 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract description 7
- 239000007789 gas Substances 0.000 description 15
- 238000004128 high performance liquid chromatography Methods 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 238000005481 NMR spectroscopy Methods 0.000 description 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 7
- 238000011946 reduction process Methods 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000007790 solid phase Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 4
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 125000005842 heteroatom Chemical group 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 238000005004 MAS NMR spectroscopy Methods 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- 229940088710 antibiotic agent Drugs 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 238000005388 cross polarization Methods 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 230000000887 hydrating effect Effects 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 229910001928 zirconium oxide Inorganic materials 0.000 description 2
- KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- BTMWJZPJQDYRFI-UHFFFAOYSA-N 2,3,3a,4-tetrahydro-1h-imidazo[4,5-c]pyridine Chemical compound C1N=CC=C2NCNC21 BTMWJZPJQDYRFI-UHFFFAOYSA-N 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- GAMYYCRTACQSBR-UHFFFAOYSA-N 4-azabenzimidazole Chemical compound C1=CC=C2NC=NC2=N1 GAMYYCRTACQSBR-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 208000035473 Communicable disease Diseases 0.000 description 1
- ASMQGLCHMVWBQR-UHFFFAOYSA-N Diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)(O)OC1=CC=CC=C1 ASMQGLCHMVWBQR-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- LINDOXZENKYESA-UHFFFAOYSA-N TMG Natural products CNC(N)=NC LINDOXZENKYESA-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- FVUCWGGFZNLYLD-UHFFFAOYSA-M [Na+].C(C=CCCCC)C(=O)[O-] Chemical compound [Na+].C(C=CCCCC)C(=O)[O-] FVUCWGGFZNLYLD-UHFFFAOYSA-M 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 241001148470 aerobic bacillus Species 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 description 1
- 208000022362 bacterial infectious disease Diseases 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940041011 carbapenems Drugs 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 125000006165 cyclic alkyl group Chemical group 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000002993 cycloalkylene group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- VILAVOFMIJHSJA-UHFFFAOYSA-N dicarbon monoxide Chemical compound [C]=C=O VILAVOFMIJHSJA-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000004475 heteroaralkyl group Chemical group 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000005633 phthalidyl group Chemical group 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- ZIHYVLFLVDRNED-UHFFFAOYSA-M sodium;2-methylhept-2-enoate Chemical group [Na+].CCCCC=C(C)C([O-])=O ZIHYVLFLVDRNED-UHFFFAOYSA-M 0.000 description 1
- 238000000279 solid-state nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 125000003107 substituted aryl group Chemical group 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
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D477/00—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
- C07D477/10—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
- C07D477/12—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2 with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6
- C07D477/16—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, and with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2 with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6 with hetero atoms or carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 3
- C07D477/20—Sulfur atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D477/00—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
- C07D477/02—Preparation
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Pharmacology & Pharmacy (AREA)
- Communicable Diseases (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Molecular Biology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
w 및 z는 0 내지 9이다.
각 (°2쎄타) | D 간격 (옹스트롬) | I/Imax (%) |
4.8 | 18.44 | 100 |
6.7 | 13.09 | 41 |
10.5 | 8.43 | 38 |
11.7 | 7.58 | 41 |
13.6 | 6.48 | 72 |
14.4 | 6.16 | 62 |
16.0 | 5.55 | 39 |
17.2 | 5.14 | 44 |
18.4 | 4.81 | 63 |
19.7 | 4.50 | 60 |
20.8 | 4.26 | 64 |
21.6 | 4.11 | 59 |
22.1 | 4.02 | 66 |
23.1 | 3.85 | 63 |
24.1 | 3.69 | 93 |
26.1 | 3.41 | 83 |
26.6 | 3.35 | 67 |
27.0 | 3.03 | 71 |
27.4 | 3.25 | 71 |
28.6 | 3.12 | 63 |
31.1 | 2.87 | 83 |
각 (°2쎄타) | D 간격 (옹스트롬) | I/Imax (%) |
4.8 | 18.48 | 59 |
6.8 | 13.02 | 24 |
7.8 | 11.27 | 21 |
10.4 | 8.50 | 49 |
11.8 | 7.51 | 34 |
13.6 | 6.51 | 55 |
14.4 | 6.13 | 51 |
15.2 | 5.82 | 27 |
17.3 | 5.13 | 32 |
18.5 | 4.78 | 58 |
19.0 | 4.67 | 64 |
19.7 | 4.50 | 62 |
20.9 | 4.24 | 58 |
21.9 | 4.06 | 100 |
23.1 | 3.85 | 39 |
24.1 | 3.69 | 46 |
24.5 | 3.63 | 65 |
26.1 | 3.41 | 51 |
26.5 | 3.36 | 37 |
26.9 | 3.31 | 34 |
27.7 | 3.22 | 75 |
28.7 | 3.11 | 32 |
30.0 | 2.98 | 33 |
31.1 | 2.87 | 47 |
32.3 | 2.77 | 49 |
각 (°2쎄타) | D 간격 (옹스트롬) | I/Imax (%) |
4.8 | 18.29 | 50 |
6.8 | 12.94 | 22 |
7.8 | 11.25 | 28 |
10.7 | 8.28 | 65 |
11.8 | 7.50 | 45 |
13.7 | 6.46 | 44 |
14.6 | 6.08 | 45 |
17.3 | 5.11 | 30 |
18.6 | 4.78 | 44 |
19.14 | 4.63 | 67 |
19.9 | 4.45 | 42 |
21.0 | 4.22 | 35 |
22.1 | 4.02 | 100 |
24.2 | 3.67 | 60 |
26.1 | 3.41 | 50 |
27.9 | 3.20 | 59 |
31.3 | 2.86 | 38 |
32.5 | 2.75 | 39 |
실시예 4
Claims (22)
- 삭제
- a) 메탄올, 에탄올, 1-프로판올, 2-프로판올, 메틸 아세테이트, 에틸 아세테이트, 이소프로필 아세테이트, 아세톤, 메틸 에틸 케톤 및 이들의 혼합물로 이루어진 그룹으로부터 선택되는 유기 용매를 함유하는 결정질 카바페넴 고형을, 1 내지 5%(w/w)의 물을 함유하는, 메틸 아세테이트, 아세토니트릴, 테트라하이드로푸란, 아세톤 및 이들의 혼합물로 이루어진 그룹으로부터 선택되는 함수 유기 용매를 사용하여 세정하여 잔류하는 상기 유기 용매를 함유하는 세정된 결정질 카바페넴 고형을 제조하는 단계; 및b) 진공 또는 불활성 기체 스트림, 또는 진공 및 불활성 기체 스트림 둘 다를 사용하여 -15 내지 20℃의 온도에서 세정된 결정질 카바페넴 고형속의 잔류 유기 용매를 증발시킴으로써, 약제학적으로 허용되는 수준의 유기 용매를 함유하는 화학식 I의 결정질 카바페넴 고형을 제조하는 단계를 포함하며, 공정 동안, 결정질 카바페넴 고형의 함수량을, 잔류 유기 용매를 조정하여 13 내지 25%로 유지시킴을 특징으로 하는, 화학식 I의 결정질 카바페넴 고형의 유기 용매의 함량을 약제학적으로 허용되는 수준으로 감소시키는 방법.화학식 I상기 화학식 I에서,R1 및 R2는 동일하거나 상이하며, H이거나, 또는 치환되지 않거나, 할로, 하이드록시, 시아노, 아실, 아실아미노, 아르알콕시, 알킬술포닐, 아릴술포닐, 알킬술포닐아미노, 아릴술포닐아미노, 알킬아미노카보닐, 알킬, 알콕시, 아릴, 아릴옥시, 아르알콕시, 아미노, 알킬아미노, 디알킬아미노, 카복시, 트리플루오로메틸, 카바모일옥시 C1-6알킬, 우레이도 C1-6알킬, 카바모일, 카바모일 C1-6알킬 또는 모노- 또는 디-C1-6알킬 카바모일C1-6알킬 및 술포닐아미노로 이루어진 그룹(이때, 치환기 중의 알킬 부분의 탄소수는 1 내지 6이고, 아릴은 페닐 또는 나프틸이다)으로부터 선택된 1-3개의 그룹으로 치환된 C1-6 알킬, C6-10 아릴 및 C5-10 헤테로아릴로부터 선택된다.
- 삭제
- 제2항에 있어서, 공정 동안 결정질 카바페넴 고형의 함수량을 16 내지 22%로 유지시키는 방법.
- 제4항에 있어서, 공정 동안, 결정질 카바페넴 고형의 함수량을 16 내지 22%로 유지시키기 위해 증발 단계를 0℃ 이하의 온도에서 진공하에 수행하거나; 0℃ 이하의 온도에서 불활성 기체 스트림을 사용하여 수행하거나; 또는 진공하에 0℃ 이하의 온도에서 불활성 기체 스트림을 사용하여 수행하거나 또는 수화된 불활성 기체 스트림을 사용하여 수행하는 방법.
- 삭제
- 제2항에 있어서, 함수 유기 용매가 2 내지 4%(w/v)의 물을 함유하는 메틸 아세테이트인 방법.
- a) 메탄올, 에탄올, 1-프로판올, 2-프로판올, 메틸 아세테이트, 에틸 아세테이트, 이소프로필 아세테이트, 아세톤, 메틸 에틸 케톤 및 이들의 혼합물로 이루어진 그룹으로부터 선택되는 유기 용매를 함유하는 화학식 II의 결정질 카바페넴 고형을, 1 내지 5%(w/v)의 물을 함유하는, 아세톤, 아세토니트릴, 테트라하이드로푸란, 메틸 아세테이트 및 이들의 혼합물로 이루어진 그룹으로부터 선택된 함수 유기 용매를 사용하여 세정하여 잔류하는 상기 유기 용매를 함유하는 화학식 II의 세정된 결정질 카바페넴 고형을 제조하는 단계; 및b) 진공 또는 불활성 기체, 또는 진공 및 불활성 기체 둘 다를 사용하여 -15 내지 20℃의 온도에서 화학식 II의 세정된 결정질 카바페넴 고형속의 잔류 유기 용매를 증발시킴으로써, 약제학적으로 허용되는 수준의 잔류 유기 용매를 함유하는 화학식 II의 결정질 카바페넴 고형을 제조하는 단계를 포함하며, 공정 동안 결정질 카바페넴 고형의 함수량을, 잔류 유기 용매를 조정하여 13 내지 25%로 유지시킴을 특징으로 하는, 화학식 II의 결정질 카바페넴 고형내의 잔류 유기 용매의 함량을 약제학적으로 허용되는 수준으로 감소시키는 방법.화학식 II상기 화학식 II에서,X+는 Na+, K+ 및 Li+로부터 선택된다.
- 삭제
- 제8항에 있어서, 증발 단계를 0℃ 이하의 온도에서 진공하에 수행하거나; 0℃ 이하의 온도에서 불활성 기체 스트림을 사용하여 수행하거나; 또는 0℃ 이하의 온도에서 불활성 기체 스트림을 사용하여 진공 하에 수행하는 방법.
- 제10항에 있어서, 불활성 기체 스트림을 사용할 경우, 불활성 기체 스트림이 질소 기체이고, 불활성 기체 스트림의 유속이 화학식 II의 화합물의 분석 그람당 0.3 내지 30SLPH(표준 리터/시)인 방법.
- 제11항에 있어서, 잔류 용매의 감소에 사용한 불활성 기체 스트림을 수화시켜 공정 동안, 결정질 카바페넴 고형의 함수량을 13 내지 25%로 유지시키는 방법.
- a) 메탄올, 에탄올, 1-프로판올, 2-프로판올, 메틸 아세테이트, 에틸 아세테이트, 이소프로필 아세테이트, 아세톤, 메틸 에틸 케톤 및 이들의 혼합물로 이루어진 그룹으로부터 선택되는 유기 용매를 함유하는 화학식 IIa의 결정질 카바페넴 고형을, 1 내지 5%(w/v)의 물을 함유하는 메틸 아세테이트를 사용하여, 세정하여 잔류하는 상기 유기 용매를 함유하는 화학식 IIa의 세정된 결정질 카바페넴 고형을 제조하는 단계; 및b) 10℃ 이하의 온도에서 화합물의 분석 그람당 0.3 내지 30SLPH(표준 리터/시)의 질소 유속으로 수화된 질소 스트림을 사용하여 진공하에 화학식 IIa의 세정된 결정질 카바페넴 고형 속의 잔류 유기 용매를 증발시킴으로써, 약제학적으로 허용되는 수준의 잔류 유기 용매를 함유하는 화학식 IIa의 결정질 카바페넴 고형을 제조하는 단계를 포함하며, 공정 동안, 결정질 카바페넴 고형의 함수량을 잔류 유기 용매를 조정하여 13 내지 25%로 유지시킴을 특징으로 하는, 화학식 IIa의 (4R, 5S, 6S, 8R, 2'S, 4'S)-3-[[2-[[3-카복시페닐)아미노]-카보닐]피롤리딘-4-일]티오]-4-메틸-6-(1-하이드록시에틸)-7-옥소-1-아자비사이클로[3.2.0]헵트-2-엔-2-카복실산 일나트륨 염의 결정질 카바페넴 고형속의 유기 용매의 함량을 감소시키는 방법.화학식 IIa
- 제13항에 있어서, 유기 용매가 메탄올, 에탄올, 1-프로판올, 2-프로판올 및 이들의 혼합물로 이루어진 그룹으로부터 선택되고; 메틸 아세테이트가 2 내지 4%(w/v)의 물을 함유하는 방법.
- 10℃ 이하의 온도에서 진공 및 화합물의 분석 그람당 0.3 내지 30SLPH(표준 리터/시간)의 질소 유속으로 수화된 질소 스트림을 사용하여, 메탄올, 에탄올, 1-프로판올, 2-프로판올, 메틸 아세테이트, 아세토니트릴, 테트라하이드로푸란, 아세톤 및 이들의 혼합물으로 이루어진 그룹으로부터 선택되는 잔류 유기 용매를 증발시킴으로써, 약제학적으로 허용되는 수준의 잔류 유기 용매를 함유하는 화학식 IIa의 결정질 카바페넴 고형을 제조함을 포함하며, 공정 동안 결정질 카바페넴 화합물의 함수량을 잔류 유기 용매를 조정하여 13 내지 25%로 유지시킴을 특징으로 하는, 고체상 X-선 분말 회절(XRPD) 패턴에서 d-간격이 18.29, 12.94, 11.25, 8.28, 7.50, 6.46, 6.08, 5.11, 4.78, 4.63, 4.45, 4.22, 4.02, 3.67, 3.41, 3.20, 2.86 및 2.75 옹스트롬임을 특징으로 하는 C형의 화학식 IIa의 (4R, 5S, 6S, 8R, 2'S, 4'S)-3-[[2-[[3-카복시페닐)아미노]-카보닐]피롤리딘-4-일]티오]-4-메틸-6-(1-하이드록시에틸)-7-옥소-1-아자비사이클로[3.2.0]헵트-2-엔-2-카복실산 일나트륨 염의 결정질 카바페넴 고형속의 잔류 유기 용매의 수준을 감소시키는 방법.화학식 IIa
- 삭제
- 삭제
- 삭제
- a) 메탄올, 에탄올, 1-프로판올, 2-프로판올, 메틸 아세테이트, 에틸 아세테이트, 이소프로필 아세테이트, 아세톤, 메틸 에틸 케톤 및 이들의 혼합물로 이루어진 그룹로부터 선택되는 유기 용매를 함유하는 결정질 카바페넴 고형을, 메탄올, 에탄올, 1-프로판올, 2-프로판올, 메틸 아세테이트, 아세톤 및 이들의 혼합물로 이루어진 그룹으로부터 선택되는 무수 유기 용매로 세정하여 잔류하는 상기 유기 용매를 함유하는 세정된 결정질 카바페넴 고형을 제조하는 단계 및b) 20℃ 이하의 온도에서 진공 및 결정질 카바페넴 고형의 함수량을 세정 및 증발 단계 동안 13 내지 25%의 수준에 이르게 하는 방식으로 수화된 불활성 기체 스트림을 사용하여 세정된 결정질 카바페넴 고형내의 잔류 유기 용매를 증발시킴으로써, 약제학적으로 허용되는 수준의 유기 용매를 함유하는 화학식 I의 결정질 카바페넴 고형을 제조하는 단계를 포함하여, 화학식 I의 결정질 카바페넴 고형 및 이의 염속의 유기 용매의 수준을 감소시키는 방법.화학식 I상기 화학식 I에서,R1 및 R2는 동일하거나 상이하며, H이거나, 또는 치환되지 않거나, 할로, 하이드록시, 시아노, 아실, 아실아미노, 아르알콕시, 알킬술포닐, 아릴술포닐, 알킬술포닐아미노, 아릴술포닐아미노, 알킬아미노카보닐, 알킬, 알콕시, 아릴, 아릴옥시, 아르알콕시, 아미노, 알킬아미노, 디알킬아미노, 카복시, 트리플루오로메틸, 카바모일옥시 C1-6알킬, 우레이도 C1-6알킬, 카바모일, 카바모일 C1-6알킬 또는 모노- 또는 디-C1-6알킬 카바모일C1-6알킬 및 술포닐아미노로 이루어진 그룹(이때, 치환기 중의 알킬 부분의 탄소수는 1 내지 6이고, 아릴은 페닐 또는 나프틸이다)으로부터 선택된 1-3개의 그룹으로 치환된 C1-6 알킬, C6-10 아릴 및 C5-10 헤테로아릴로부터 선택된다.
- 제19항에 있어서, 수화된 불활성 기체가 질소인 방법.
- 삭제
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US32513001P | 2001-09-26 | 2001-09-26 | |
US60/325,130 | 2001-09-26 | ||
PCT/US2002/029879 WO2003027067A2 (en) | 2001-09-26 | 2002-09-20 | Process for making carbapenem compounds |
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KR1020047004533A KR100628676B1 (ko) | 2001-09-26 | 2002-09-20 | 카바페넴 화합물의 제조방법 |
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US (1) | US7022841B2 (ko) |
EP (1) | EP1474426B8 (ko) |
JP (1) | JP4480396B2 (ko) |
KR (1) | KR100628676B1 (ko) |
CN (2) | CN100338064C (ko) |
AT (1) | ATE518864T1 (ko) |
AU (1) | AU2002341747B2 (ko) |
BR (1) | BRPI0212411B8 (ko) |
CA (1) | CA2461565C (ko) |
CY (1) | CY1112092T1 (ko) |
DK (1) | DK1474426T3 (ko) |
EA (1) | EA008168B1 (ko) |
ES (1) | ES2368997T3 (ko) |
HU (1) | HU230700B1 (ko) |
IL (1) | IL160413A0 (ko) |
MX (1) | MXPA04002797A (ko) |
NZ (1) | NZ531174A (ko) |
PL (1) | PL218808B1 (ko) |
PT (1) | PT1474426E (ko) |
RS (1) | RS52410B (ko) |
UA (1) | UA78524C2 (ko) |
WO (1) | WO2003027067A2 (ko) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2003026572A2 (en) * | 2001-09-26 | 2003-04-03 | Merck & Co., Inc. | Crystalline forms of ertapenem sodium |
PL368984A1 (en) * | 2001-11-16 | 2005-04-04 | Ranbaxy Laboratories Limited | Process for the preparation of crystalline imipenem |
MX2007006018A (es) * | 2004-11-30 | 2007-06-07 | Astellas Pharma Inc | Suspension farmaceutica oral novedosa de cristal de cefdinir. |
CN100457760C (zh) * | 2005-10-20 | 2009-02-04 | 上海交通大学 | 尔他培南钠盐的制备方法 |
US8293894B2 (en) * | 2006-11-20 | 2012-10-23 | Orchid Chemicals & Pharmaceuticals Limited | Process for the preparation of carbapenem antibiotic |
CN101367812B (zh) * | 2007-06-28 | 2011-04-27 | 山东轩竹医药科技有限公司 | 被巯基吡咯烷甲酰胺基环戊烯酸取代的培南衍生物 |
CN101372490B (zh) * | 2007-08-15 | 2011-02-09 | 山东轩竹医药科技有限公司 | 含有巯基氮杂环乙烯基氮杂环的培南衍生物 |
US20110172201A1 (en) * | 2008-06-11 | 2011-07-14 | Ranbaxy Laboratories Limited | Process for preparing a carbapenem antibiotic composition |
CN102558182B (zh) | 2010-12-31 | 2015-02-11 | 石药集团中奇制药技术(石家庄)有限公司 | 一种厄他培南钠晶型及其制备方法 |
CN102363617B (zh) * | 2011-11-09 | 2013-09-18 | 上海希迈医药科技有限公司 | 一种厄他培南单钠盐结晶体及其制备方法 |
US20150038726A1 (en) * | 2012-04-04 | 2015-02-05 | Hospira, Inc. | Process for the preparation of carbapenem antibiotic |
IN2013MU03862A (ko) | 2013-12-11 | 2015-07-31 | Unimark Remedies Ltd | |
CN113416193B (zh) * | 2021-08-23 | 2021-12-17 | 凯莱英医药集团(天津)股份有限公司 | 厄他培南钠新晶型及其制备方法 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1283906C (en) * | 1983-05-09 | 1991-05-07 | Makoto Sunagawa | .beta.-LACTAM COMPOUNDS AND PRODUCTION THEREOF |
IE60588B1 (en) | 1986-07-30 | 1994-07-27 | Sumitomo Pharma | Carbapenem compound in crystalline form, and its production and use |
JP3048196B2 (ja) * | 1991-06-20 | 2000-06-05 | 第一製薬株式会社 | カルバペネム誘導体 |
GB9202298D0 (en) | 1992-02-04 | 1992-03-18 | Ici Plc | Antibiotic compounds |
CZ290002B6 (cs) * | 1992-03-11 | 2002-05-15 | Sankyo Company Limited | Antimikrobiální karbapenemové deriváty, způsob výroby a farmaceutický prostředek |
ZA938438B (en) * | 1992-11-17 | 1994-06-20 | Sankyo Co | Crystalline carbapenem derivative |
DE69714841T2 (de) * | 1996-04-26 | 2003-05-28 | Sankyo Co | Ein 1-methylcarbapenem-derivat |
US6180783B1 (en) | 1997-06-16 | 2001-01-30 | Merck & Co., Inc. | Stabilized carbapenem intermediates and improved process for carbapenem synthesis |
US5872250A (en) | 1997-07-30 | 1999-02-16 | Merck & Co., Inc. | Process for synthesizing carbapenem antibiotics |
JP3953274B2 (ja) | 1998-03-02 | 2007-08-08 | メルク エンド カムパニー インコーポレーテッド | カルバペネム抗生物質の合成方法 |
TWI250160B (en) * | 1999-07-06 | 2006-03-01 | Sankyo Co | Crystalline 1-methylcarbapenem compound |
AR035728A1 (es) * | 2001-01-16 | 2004-07-07 | Merck & Co Inc | Proceso perfeccionado para la sintesis de carbapenem |
WO2003026572A2 (en) * | 2001-09-26 | 2003-04-03 | Merck & Co., Inc. | Crystalline forms of ertapenem sodium |
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