GB2162185A - New process for preparation of substituted penem derivatives - Google Patents
New process for preparation of substituted penem derivatives Download PDFInfo
- Publication number
- GB2162185A GB2162185A GB08520253A GB8520253A GB2162185A GB 2162185 A GB2162185 A GB 2162185A GB 08520253 A GB08520253 A GB 08520253A GB 8520253 A GB8520253 A GB 8520253A GB 2162185 A GB2162185 A GB 2162185A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- formula
- compound
- penem
- hydroxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims description 46
- 238000002360 preparation method Methods 0.000 title claims description 13
- 150000002961 penems Chemical class 0.000 title description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 174
- 150000003839 salts Chemical class 0.000 claims abstract description 40
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 27
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 9
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 9
- 125000004076 pyridyl group Chemical group 0.000 claims abstract description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 6
- 125000000962 organic group Chemical group 0.000 claims abstract description 5
- -1 amino, hydroxy Chemical group 0.000 claims description 126
- 239000000203 mixture Substances 0.000 claims description 89
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 53
- 125000001424 substituent group Chemical group 0.000 claims description 23
- 229910052739 hydrogen Inorganic materials 0.000 claims description 21
- 150000002148 esters Chemical class 0.000 claims description 20
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 19
- 239000001257 hydrogen Substances 0.000 claims description 19
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 125000003396 thiol group Chemical class [H]S* 0.000 claims description 12
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 8
- 125000002252 acyl group Chemical group 0.000 claims description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 8
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- 239000011574 phosphorus Substances 0.000 claims description 7
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims description 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims description 5
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 5
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000002883 imidazolyl group Chemical group 0.000 claims description 3
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- USVVENVKYJZFMW-ONEGZZNKSA-N (e)-carboxyiminocarbamic acid Chemical compound OC(=O)\N=N\C(O)=O USVVENVKYJZFMW-ONEGZZNKSA-N 0.000 claims description 2
- 125000004511 1,2,3-thiadiazolyl group Chemical group 0.000 claims description 2
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 claims description 2
- 125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004185 ester group Chemical group 0.000 claims description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 2
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- KPSSIOMAKSHJJG-UHFFFAOYSA-N neopentyl alcohol Chemical compound CC(C)(C)CO KPSSIOMAKSHJJG-UHFFFAOYSA-N 0.000 claims 2
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract description 3
- 239000003242 anti bacterial agent Substances 0.000 abstract description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 138
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 129
- 239000000243 solution Substances 0.000 description 109
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 86
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 74
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 72
- 239000000047 product Substances 0.000 description 58
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 56
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 52
- 235000019439 ethyl acetate Nutrition 0.000 description 49
- 235000017557 sodium bicarbonate Nutrition 0.000 description 36
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 36
- 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 35
- 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 34
- 239000011734 sodium Substances 0.000 description 34
- 229910052708 sodium Inorganic materials 0.000 description 33
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 32
- 229940093499 ethyl acetate Drugs 0.000 description 31
- 238000000926 separation method Methods 0.000 description 29
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 28
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 27
- 238000003756 stirring Methods 0.000 description 27
- 239000012071 phase Substances 0.000 description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 24
- 239000002904 solvent Substances 0.000 description 24
- 238000006243 chemical reaction Methods 0.000 description 23
- 230000002441 reversible effect Effects 0.000 description 21
- 239000007787 solid Substances 0.000 description 18
- 239000000741 silica gel Substances 0.000 description 17
- 229910002027 silica gel Inorganic materials 0.000 description 17
- 239000002253 acid Substances 0.000 description 16
- 239000012074 organic phase Substances 0.000 description 15
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 14
- 239000003921 oil Substances 0.000 description 14
- 235000019198 oils Nutrition 0.000 description 14
- 239000011541 reaction mixture Substances 0.000 description 14
- VEPTXBCIDSFGBF-UHFFFAOYSA-M tetrabutylazanium;fluoride;trihydrate Chemical compound O.O.O.[F-].CCCC[N+](CCCC)(CCCC)CCCC VEPTXBCIDSFGBF-UHFFFAOYSA-M 0.000 description 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 13
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 12
- 159000000000 sodium salts Chemical class 0.000 description 12
- MHYGQXWCZAYSLJ-UHFFFAOYSA-N tert-butyl-chloro-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](Cl)(C(C)(C)C)C1=CC=CC=C1 MHYGQXWCZAYSLJ-UHFFFAOYSA-N 0.000 description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 10
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 10
- 239000008346 aqueous phase Substances 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 10
- 239000000706 filtrate Substances 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- 239000006260 foam Substances 0.000 description 9
- 239000012044 organic layer Substances 0.000 description 9
- 239000000725 suspension Substances 0.000 description 9
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 8
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 8
- WACQKHWOTAEEFS-UHFFFAOYSA-N cyclohexane;ethyl acetate Chemical compound CCOC(C)=O.C1CCCCC1 WACQKHWOTAEEFS-UHFFFAOYSA-N 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 238000012544 monitoring process Methods 0.000 description 8
- 125000006239 protecting group Chemical group 0.000 description 8
- 239000006188 syrup Substances 0.000 description 8
- 235000020357 syrup Nutrition 0.000 description 8
- KPTNUCBVMWICQI-UHFFFAOYSA-N 1-methyl-2h-tetrazole-5-thione;sodium Chemical compound [Na].CN1NN=NC1=S KPTNUCBVMWICQI-UHFFFAOYSA-N 0.000 description 7
- FAMRKDQNMBBFBR-BQYQJAHWSA-N diethyl azodicarboxylate Substances CCOC(=O)\N=N\C(=O)OCC FAMRKDQNMBBFBR-BQYQJAHWSA-N 0.000 description 7
- 238000010828 elution Methods 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 7
- 238000006460 hydrolysis reaction Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000001241 acetals Chemical class 0.000 description 6
- 125000004423 acyloxy group Chemical group 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- FAMRKDQNMBBFBR-UHFFFAOYSA-N ethyl n-ethoxycarbonyliminocarbamate Chemical compound CCOC(=O)N=NC(=O)OCC FAMRKDQNMBBFBR-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 230000002829 reductive effect Effects 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 6
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- NOTFZGFABLVTIG-UHFFFAOYSA-N Cyclohexylethyl acetate Chemical compound CC(=O)OCCC1CCCCC1 NOTFZGFABLVTIG-UHFFFAOYSA-N 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 239000012267 brine Substances 0.000 description 5
- 238000004440 column chromatography Methods 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 5
- LKHYFCSSVZVVNF-UHFFFAOYSA-N ethyl hexanoate;sodium Chemical compound [Na].CCCCCC(=O)OCC LKHYFCSSVZVVNF-UHFFFAOYSA-N 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 125000004942 pyridazin-6-yl group Chemical group N1=NC=CC=C1* 0.000 description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
- ARIXWPAHBVNAIR-HIQLJADVSA-M sodium;(5r,6s)-6-[(1r)-1-hydroxyethyl]-3-(hydroxymethyl)-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate Chemical compound [Na+].S1C(CO)=C(C([O-])=O)N2C(=O)[C@H]([C@H](O)C)[C@H]21 ARIXWPAHBVNAIR-HIQLJADVSA-M 0.000 description 5
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 238000004108 freeze drying Methods 0.000 description 4
- 125000002911 monocyclic heterocycle group Chemical group 0.000 description 4
- 235000011118 potassium hydroxide Nutrition 0.000 description 4
- 238000010898 silica gel chromatography Methods 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- YDUMMNHBVKAQJT-ZXWJAXLNSA-N (5R,6S)-3-(hydroxymethyl)-6-[(1R)-1-[(4-nitrophenyl)methoxycarbonyloxy]ethyl]-5-[(4-nitrophenyl)methyl]-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid Chemical compound O([C@H](C)[C@@H]1[C@]2(SC(CO)=C(C(O)=O)N2C1=O)CC=1C=CC(=CC=1)[N+]([O-])=O)C(=O)OCC1=CC=C([N+]([O-])=O)C=C1 YDUMMNHBVKAQJT-ZXWJAXLNSA-N 0.000 description 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 101150041968 CDC13 gene Proteins 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- 241000588724 Escherichia coli Species 0.000 description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 125000002618 bicyclic heterocycle group Chemical group 0.000 description 3
- 229910052681 coesite Inorganic materials 0.000 description 3
- 229910052906 cristobalite Inorganic materials 0.000 description 3
- 238000005828 desilylation reaction Methods 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000008241 heterogeneous mixture Substances 0.000 description 3
- 150000007529 inorganic bases Chemical class 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 150000007530 organic bases Chemical class 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 159000000001 potassium salts Chemical class 0.000 description 3
- 230000000063 preceeding effect Effects 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 229910052682 stishovite Inorganic materials 0.000 description 3
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 229910052905 tridymite Inorganic materials 0.000 description 3
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- SPXJIFUTKXLRFM-ZXWJAXLNSA-N (5R,6S)-3-(chloromethyl)-6-[(1R)-1-[(4-nitrophenyl)methoxycarbonyloxy]ethyl]-5-[(4-nitrophenyl)methyl]-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid Chemical compound [N+](=O)([O-])C1=CC=C(C[C@@]23N(C(=C(S2)CCl)C(=O)O)C([C@@H]3[C@@H](C)OC(=O)OCC3=CC=C(C=C3)[N+](=O)[O-])=O)C=C1 SPXJIFUTKXLRFM-ZXWJAXLNSA-N 0.000 description 2
- YZKMRHWQKBBKKH-NGILUBTISA-N (5R,6S)-6-[(1R)-1-[(4-nitrophenyl)methoxycarbonyloxy]ethyl]-5-[(4-nitrophenyl)methyl]-7-oxo-3-(3-oxobutanoyloxymethyl)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid Chemical compound C[C@H]([C@H]1C(=O)N2[C@@]1(SC(=C2C(=O)O)COC(=O)CC(=O)C)CC3=CC=C(C=C3)[N+](=O)[O-])OC(=O)OCC4=CC=C(C=C4)[N+](=O)[O-] YZKMRHWQKBBKKH-NGILUBTISA-N 0.000 description 2
- UWUGSKDMNCXWDF-JIYNIHLBSA-N (5R,6S)-6-[(1R)-1-hydroxyethyl]-3-(hydroxymethyl)-5-[(4-nitrophenyl)methyl]-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid Chemical compound C([C@@]12SC(CO)=C(C(O)=O)N2C(=O)[C@@H]1[C@H](O)C)C1=CC=C([N+]([O-])=O)C=C1 UWUGSKDMNCXWDF-JIYNIHLBSA-N 0.000 description 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 2
- 125000006528 (C2-C6) alkyl group Chemical group 0.000 description 2
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- 125000005336 allyloxy group Chemical group 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- HOPRXXXSABQWAV-UHFFFAOYSA-N anhydrous collidine Natural products CC1=CC=NC(C)=C1C HOPRXXXSABQWAV-UHFFFAOYSA-N 0.000 description 1
- 239000008365 aqueous carrier Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 102000006635 beta-lactamase Human genes 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- JZUVESQYEHERMD-UHFFFAOYSA-N bis[(4-nitrophenyl)methyl] carbonate Chemical compound C1=CC([N+](=O)[O-])=CC=C1COC(=O)OCC1=CC=C([N+]([O-])=O)C=C1 JZUVESQYEHERMD-UHFFFAOYSA-N 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- NHYXMAKLBXBVEO-UHFFFAOYSA-N bromomethyl acetate Chemical compound CC(=O)OCBr NHYXMAKLBXBVEO-UHFFFAOYSA-N 0.000 description 1
- 206010006451 bronchitis Diseases 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 206010008323 cervicitis Diseases 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 1
- 238000011097 chromatography purification Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- UTBIMNXEDGNJFE-UHFFFAOYSA-N collidine Natural products CC1=CC=C(C)C(C)=N1 UTBIMNXEDGNJFE-UHFFFAOYSA-N 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000013058 crude material Substances 0.000 description 1
- 239000012043 crude product Substances 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
- UFULAYFCSOUIOV-UHFFFAOYSA-N cysteamine Chemical compound NCCS UFULAYFCSOUIOV-UHFFFAOYSA-N 0.000 description 1
- 201000003146 cystitis Diseases 0.000 description 1
- 230000000249 desinfective effect Effects 0.000 description 1
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 description 1
- WBKFWQBXFREOFH-UHFFFAOYSA-N dichloromethane;ethyl acetate Chemical compound ClCCl.CCOC(C)=O WBKFWQBXFREOFH-UHFFFAOYSA-N 0.000 description 1
- 235000015872 dietary supplement Nutrition 0.000 description 1
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical class [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 1
- PXCXMTKJRYTWQE-UHFFFAOYSA-L disodium;(5-sulfanylidene-2h-tetrazol-1-yl)methanesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)CN1NN=NC1=S.[O-]S(=O)(=O)CN1NN=NC1=S PXCXMTKJRYTWQE-UHFFFAOYSA-L 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000006196 drop Substances 0.000 description 1
- 208000019258 ear infection Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000010931 ester hydrolysis Methods 0.000 description 1
- LJQKCYFTNDAAPC-UHFFFAOYSA-N ethanol;ethyl acetate Chemical compound CCO.CCOC(C)=O LJQKCYFTNDAAPC-UHFFFAOYSA-N 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 1
- OAMZXMDZZWGPMH-UHFFFAOYSA-N ethyl acetate;toluene Chemical compound CCOC(C)=O.CC1=CC=CC=C1 OAMZXMDZZWGPMH-UHFFFAOYSA-N 0.000 description 1
- SLFUXNFVAANERW-UHFFFAOYSA-N ethyl hexanoate;potassium Chemical compound [K].CCCCCC(=O)OCC SLFUXNFVAANERW-UHFFFAOYSA-N 0.000 description 1
- 238000003818 flash chromatography Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 235000011167 hydrochloric acid Nutrition 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000007927 intramuscular injection Substances 0.000 description 1
- 238000010255 intramuscular injection Methods 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine 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
- 239000008101 lactose Substances 0.000 description 1
- 229960004393 lidocaine hydrochloride Drugs 0.000 description 1
- YECIFGHRMFEPJK-UHFFFAOYSA-N lidocaine hydrochloride monohydrate Chemical compound O.[Cl-].CC[NH+](CC)CC(=O)NC1=C(C)C=CC=C1C YECIFGHRMFEPJK-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229960003151 mercaptamine Drugs 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229960003966 nicotinamide Drugs 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 125000004043 oxo group Chemical group O=* 0.000 description 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 229950009506 penicillinase Drugs 0.000 description 1
- 150000002960 penicillins Chemical class 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- IPNPIHIZVLFAFP-UHFFFAOYSA-N phosphorus tribromide Chemical compound BrP(Br)Br IPNPIHIZVLFAFP-UHFFFAOYSA-N 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 208000008423 pleurisy Diseases 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 229940007042 proteus vulgaris Drugs 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 208000020029 respiratory tract infectious disease Diseases 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 208000013223 septicemia Diseases 0.000 description 1
- 238000005055 short column chromatography Methods 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 201000009890 sinusitis Diseases 0.000 description 1
- WGGAAWXHXJXNEU-BAEOHNDXSA-M sodium (5R,6S)-6-[(1R)-1-hydroxyethyl]-3-[(4-methyl-5,6-dioxo-1H-1,2,4-triazin-3-yl)sulfanylmethyl]-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate Chemical compound [Na+].O[C@H](C)[C@@H]1[C@@H]2N(C(=C(S2)CSC2=NN=C(C(N2C)=O)O)C(=O)[O-])C1=O WGGAAWXHXJXNEU-BAEOHNDXSA-M 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- MSCCCPDQSMQINS-ODYOSOFBSA-M sodium;(5r,6s)-6-[(1r)-1-hydroxyethyl]-3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate Chemical compound [Na+].S([C@@H]1[C@H](C(N1C=1C([O-])=O)=O)[C@H](O)C)C=1CSC1=NN=NN1C MSCCCPDQSMQINS-ODYOSOFBSA-M 0.000 description 1
- UCPONNNCHGVWOA-UHFFFAOYSA-N sodium;5h-tetrazolo[1,5-b]pyridazine-6-thione Chemical compound [Na].N1C(=S)C=CC2=NN=NN21 UCPONNNCHGVWOA-UHFFFAOYSA-N 0.000 description 1
- WZWGGYFEOBVNLA-UHFFFAOYSA-N sodium;dihydrate Chemical compound O.O.[Na] WZWGGYFEOBVNLA-UHFFFAOYSA-N 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000004299 tetrazol-5-yl group Chemical group [H]N1N=NC(*)=N1 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 125000005039 triarylmethyl group Chemical group 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 208000019206 urinary tract infection Diseases 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D499/88—Compounds with a double bond between positions 2 and 3 and 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Compounds of the formula I <IMAGE> where R1 is H or an organic group R2 is a carboxy protecting group and Y is -S-Het where het is a heterocyclic ring or alkylthio or pyridyl are prepared by reacting <IMAGE> with Y-H where L is Cl, Br or OH or an activated OH. The compounds I and their pharmaceutically acceptable salts find use as an anti-bacterial agents.
Description
SPECIFICATION
Substituted penem derivatives and new process for their preparation
The present invention relates to a new process for the preparation of substituted penems and to new penem compounds and process for their preparation and pharmaceutical and veterinary compositions containing them.
A first object of the invention is a new process for the preparation of compounds of formula (I)
wherein
R1 is hydrogen or an organic group;
R2 is hydrogen or a carboxy protecting group; and
Y is
a) a group -S-Het wherein Het is an optionally substituted saturated or unsaturated heterocyclic ring containing at least one heteroatom chosen from 0, S and N;
b) a formyloxy or a C2-C6 carboxylic acyloxy group wherein the acyl group may be unsubstituted or substituted by halogen, C,-C, carboxylic acyl, amino, hydroxy or mercapto and wherein the amino, hydroxy and mercapto groups may optionally be in a protected form;;
c) a C1-C12 alkoxy or C1-C12 alkylthio group both optionally substituted by one or more substituents chosen from halogen, formyl, C2-C6 acyl, amino, hydroxy and mercapto, wherein the amino, hydroxy and mercapto groups may optionally be in a protected form;
d) an optionally substituted pyridyl group; or
e) acid; and the pharmaceutically or veterinarily acceptable salts of the compounds of formula (I).
Another object of the invention concerns new penem derivatives falling within the scope of formula (I) and pharmaceutically or veterinarily acceptable salts thereof, a process for their preparation, and pharmaceutical or veterinary compositions containing said new penem derivatives.
In the above formula (I) the organic group R1 is especially an optionally substituted aliphatic or cycloaliphatic hydrocarbon group.
When R1 is an aliphatic hydrocarbon group it is preferably a C1-C12 alkyl group, optionally substituted by one or more substituents chosen from hydroxy, amino, cyano and mercapto, wherein the hydroxy, amino and mercapto groups may be free or protected.
Preferred alkyl groups for B are methyl and ethyl, in particular ethyl, and a particularly preferred substituent on such groups is an optionally protected hydroxy. When R1 is a cycloaliphatic hydrocarbon group it is, preferably a 04-C, monocycloalkyl group, in particular cyclopentyl or cyclohexyl, optionally substituted by one or more substituents chosen from C1-C6 alkyl, for example methyl or ethyl, hydroxy, amino, cyano, and mercapto groups, the hydroxy, amino and mercapto groups being free or protected.
When R2 is a carboxy protecting group it may be any group which, together with the -COO- moiety, forms an esterified carboxy group. Examples of carboxy protecting groups R2 are, in particular, C,-C6 alkyl groups, for instance methyl, ethyl or tert-butyl; halo-substituted C,-C, alkyl groups, for example 2,2,2trichloroethyl; C2-C4 alkenyl groups, for example allyl; optionally substituted aryl groups, for example phenyl and p-nitro-phenyl; optionally substituted aryl-C1-C6 alkyl groups, for example benzyl, p-nitro-benzyl and p-methoxy-benzyl; aryloxy-Ci-Ce alkyl groups, for example phenoxy-methyl; or groups such as benzyhydryl, o-nitro-benyhydryl, acetonyl, trimethylsilyl, diphenyl-tert-butyl-silyl, and dimethyl-tert-butyl-silyl.
The definition of R2 as a carboxy protecting group includes also any residue, such as for instance acetoxymethyl, pivaloyloxymethyl or phtalidyl, leading to an ester group which is known to be hydrolized "in vivo" and to have favourable pharmacokinetic properties.
When Y is a group -S-Het as defined above, the group Het is, especially:
A) a pentatomic or hexatomic heteromonocyclic ring, containing at least one double bond and at least one heteroatom selected from N, S and 0, unsubstituted or substituted by one or more substituents selected from:
a') hydroxy, C1-C6 alkoxy, halogen, C2-C6 aliphatic acyl;
b') Cl-C6 alkyl unsubstituted or substituted by a tetrazolyl group or by one or more substituents selected from hydroxy and halogen;
c') C2-C6 alkenyl unsubstituted or substituted by one or more substituents selected from hydroxy and halogen;
d') -S-R3 wherein R3 is hydrogen or C1-C6 alkyl; or -S-CH2-COOR4 wherein R4 is hydrogen, C1-C6 alkyl or a carboxy-protecting group;
e') -(CH2)n-COOR4 or -CH=CH-COOR4 wherein m is zero, 1, 2 or 3 and R4 is as defined above; -(CH2),,-CN or -(CH2),n-CONH2 wherein m is as defined above; -(CH2),,-SO2H wherein m is as defined above or
f') -(CH2),,,-N = 6R66 wherein m is as defined above, and each of R5 and R6, which may be the same or different, represents hydrogen, C1-C6 alkyl, sulpho or an aliphatic acyl group or, when one of R5 and R6 is hydrogen, the other may be also an amino protecting group; or
B) a heterobicyclic ring, containing at least two double bonds wherein each of the condensed heteromonocyclic rings, being the same or different, is a pentatomic or hexatomic heteromonocyclic ring containing at least one heteroatom selected from N, S and 0, said heterobicyclic ring being unsubstituted or substituted by one ore more substituents selected from a'), b'), c'), d'), e') and f') as defined above.
In the above definitions A) and B), preferred halogens are chlorine, bromine and iodine; preferred C1-C6 alkyl groups are methyl and ethyl; a preferred C2-C6 alkenyl group is allyl; a preferred aliphatic acyl group is acetyl; a carboxy protecting group may be any of the groups previously indicated for the R2 substituent; and the free sulpho and carboxy groups possibly present may be salified, e.g. as sodium or potassium salts.
A heteromonocyclic ring of the above class A) may be, for example, an optionally substitutedthiazolyl, triazolyl, thiadiazolyl, tetrazolyl, imidazolyl, pyrazinyl or triazinyl ring. Preferred substituents on such rings are, for example, one or more substituents chosen from amino, hydroxy, oxo, -S-CH2-COOH, a C1-C6 alkoxy and a C1-C6-alkyl group, preferably methyl or ethyl, wherein the C1-C6-alkyl group may be optionally substituted by a substituent chosen from carboxy, sulpho, cyano, carbamoyl, amino, methylamino, dimethyl-amino or sulfoamino.
A heterobicyclic ring of the above class B) may be, for example, a tetrazolopyridazinyl radical optionally substituted by amino or carboxy.
When Y is a C2-C6 carboxylic acyloxy group, the acyl group is, preferably, a C2-C6 aliphatic acyl, in particular acetyl, either unsubstituted or in its turn substituted by a C2-C6 acyl group, preferably an aliphatic acyl, in particular acetyl.
When Y is a C,-C,2 alkoxy or Cl-Cl2 alkylthio group, C,-C4 alkoxy and C1-C6 alkylthio groups are preferred, in particular methoxy, ethoxy, methylthio and ethylthio, optionally substituted as reported above.
A particularly preferred substituted C1-C6 alkylthio group is, for example, ethylthio substituted by amino.
When Y is unsubstituted pyridyl it is, preferably, 1-pyridyl.
When Y is a substituted pyridyl group it is, preferably, a 1-pyridyl group substituted by carbamoyl, in particular 4-carbamoyl.
In the above formula (I) the amino, hydroxy or mercapto protecting groups possibly present may be those usually employed in the chemistry of penicillins and cephalosporins for this kind of functions. They may be, for instance optionally substituted, especially halo-substituted, acyl groups, e.g. acetyl, monochloroacetyl, dichloroacetyl, trifluoroacetyl, benzoyl or p-bromophenacyl; triarylmethyl groups, in particular triphenylmethyl; silyl groups, in particular trimethylsilyl, dimethyl-tert-butyl-silyl, diphenyl-tert-butyl silyl; or also groups such as tert-butoxy carbonyl, p-nitro-benzyloxycarbonyl 2,2,2-trichloroethoxycarbonyl, benzyl, and pyranyl.
When, in particular, the R, substituent in formula (I) is an alkyl group substituted by hydroxy, preferred protecting groups of the hydroxy function are p-nitrobenzyloxycarbonyl; dimethyl-tert-butyl silyl; di phenyl-tert-butyl silyl; trimethyl silyl; 2,2,2-trichloroethoxycarbonyl; benzyl; p-bromo-phenacyl; triphenylmethyl and pyranyl. All the alkyl and alkenyl groups, including the aliphatic hydrocarbon moiety of the alkoxy, alkylthio and acyloxy groups, may be branched or straight. As already reported, also the pharmaceutically or veterinarily acceptable salts of the compound of formula (I) may be prepared according to the process of the invention. The said salts may be both salts with acids, either inorganic acids such as, e.g., hydrochloric or sulphuric acids, or organic acids such as e.g., citric, tartaric, fumaric or methanesulphonic acid, and salts with bases, either inorganic bases such as, e.g., alkali or alkaline-earth metal hydroxides in particular sodium and potassium hydroxides, or organic bases such as, e.g., triethylamine, pyridine, benzylamine or collidine.
Preferred salts are the salts of the compounds of formula (I) wherein R2 is hydrogen with one of the bases hereabove specified, in particular with sodium hydroxide or potassium hydroxide.
All the possible isomers of formula (I), both geometrical and optical isomers, and their mixtures, may be obtained by the new process of the invention. Preferred isomers of formula (I) are those having the 5(R) configuration and when, according to a preferred feature of the invention R1 is an hydroxy substituted ethyl group, the (5R, 6S, 8R) and (5R, 6R, 8S), in particular (5R, 6S, 8R), configurations are the preferred ones.
According to the new process which is the first object of the invention the compounds of formula (I) are prepared by reacting a compound of formula (II)
wherein R, and R2 are as defined above and L is chlorine, bromine or a free or activated hydroxy group, with a compound of formula (III)
Y- H (III) wherein Y is as defined above, or a salt thereof, or a reactive derivative thereof, and, if desired, converting an obtained compound of formula (I) into another compound of formula (I) and/or, if desired, salifying a free co-mpound of formula (I) or, if desired, obtaining a free compound of formula (I) from a salt thereof and/or, if desired separating a mixture of isomers of formula (I) into the single isomers.
An activated hydroxy group L in a compound of formula (II) is a hydroxy group activated in the form of a reactive ester or reactive complex or reactive acetal. A reactive derivative of a compound of formula (III) is either a compound of formula (III) wherein Y is -S-Het and wherein the mercapto group of the corresponding compound Het-S-H is in an activated form, or a compound of formula (III) wherein Y is formyloxy or a C2-C6 carboxylic acyloxy and wherein the carboxy group of the corresponding carboxylic acid is in an activated form.
A reactive derivative of a compound of formula (III), as herein before defined, is used only for the reaction with a compound of formula (II) wherein L is a free hydroxy group. For the reaction with a compound of formula (II) wherein L is chlorine or bromine or an activated hydroxy group, the compound of formula (lil) is preferably used as such or as a salt.
When the hydroxy group- L in the compound of formula (II) is activated in the form of a reactive ester, this may be an ester with a sulphonic acid, e.g. methanesulphonic, p-toluenesulphonic, trifluoromethanesulphonic or p-bromobenzene-sulphonic acid; or an ester with a phosphoric acid, e.g. a diaryl phosphoric acid, in particular diphenylphosphoric acid; or an ester with a carboxylic acid, e.g. acetic or acetoacetic acid.
When the hydroxy group L is activated in the form of a reactive complex, this may be, for instance, a phosphorous complex between the compound of formula (II) wherein L is hydroxy and the addition product of a derivative of trivalent phosphorus with C1-C6-alkyl ester of the azodicarboxylic acid: this addition product may be, for example, an aryl-, e.g. phenyl -, or C,-Cl alkyl-derivative of trivalent phosphorus, triphenylphosphine or tributylphosphine for instance, combined with diethyl azo-dicarboxylate.
When the hydroxy group L is activated in the form of a reactive acetal, this may be, for example, the mixed acetal between the compound of formula (II) wherein L is hydroxy, a C1-C5 aliphatic, e.g. neopentylic, alcohol, and dimethyl-formamide.
Preferably the hydroxy group L in a compound of formula (II) is activated in the form of a reactive ester thereof with a sulphonic acid, e.g. one of those hereabove mentioned, or in the form of a reactive complex with a trivalent phosphorus derivative and a C,-C6 alkyl azo-dicarboxylate, e.g. of the type hereabove mentioned.
A reactive derivative of a compound of formula (III) wherein Y is -S-Het, i.e. a compound of formula
Het-S-H, is, preferably, a complex between the corresponding disulfide Het-S-S-Het, wherein the two groups Het are the same, and an aryl-or C1-CG-alkyl-derivative of trivalent phosphorus, e.g. of the kind before specified, in particular, for example, tributylphosphine.
A reactive derivative of a compound of formula (III) wherein Y is formyloxy or C2-C6 carboxylic acyloxy, which is a carboxylic acid, may be, for instance, a corresponding halide, in particular chloride or bromide, or the anhydride or a mixed anhydride.
A salt of a compound of formula (III) may be the salt with an inorganic base such as, e.g., an alkali or alkaline-earth metal hydroxide, preferably the sodium or potassium hydroxide, or the salt with an organic base such as, e.g., triethylamine or N,N-diisopropylethylamine.
The reaction between a compound of formula (II) and a compound of formula (III), or a salt thereof, or a reactive derivative thereof, may be performed in a suitable organic solvent which may be, for instance, tetrahydrofuran, dimethylformamide, acetone or a halogenated hydrocarbon such as, e.g. dichloromethane.
The reaction temperature may, preferably, vary between about -40"C and about +40"C; preferably between -20 C and -10'C. Sometimes, for instance in the case when a compound of formula (III) is used as such, the presence of a base, such as, for instance, triethylamine or pyridine, may be required.
When, for the reaction with a compound of formula (III) or a salt thereof, a compound of formula (II) is used wherein L is chlorine or bromine or a hydroxy group activated in the form of a reactive ester with a sulphonic or phosphoric acid, of the kind specified above, any compound of formula (I), i.e. with any value of the Y substituent, may be obtained.
When, for the reaction with a compound of formula (III) or a salt thereof, a compound of formula (II) is used wherein L is a hydroxy group activated in the form of a reactive ester with a carboxylic acid as before specified, a compound of formula (I) wherein Y is -S-Het, wherein Het is as defined above may be obtained. When the starting material is a compound of formula (II) wherein the hydroxy group L is activated in the form of a reactive complex or reactive acetal of the kind previously described, a compound of formula (I) wherein Y is -S-Het, wherein Het is as defined above, or Y is optionally substituted C,-C,2 alkylthio, may be obtained.
As is evident from what reported before, the reaction of a compound of formula (II) wherein L is a free hydroxy group with a reactive derivative of a compound of formula (III) leads, according to the possible values of Y in the compound (III), either to a compound of formula (I) wherein Y is -S-Het, wherein Het is as defined above, or to a compound of formula (I) wherein Y is formyloxy or C2-C6 carboxylic acyloxy.
According to a preferred feature, the new process of the invention is used to prepare compounds of formula (I) wherein Y is an optionally substituted group -S-Het, wherein Het is as defined above, either
a) by reacting a compound of formula (III) wherein Y is S-Het, or a salt thereof, with a compound of formula (II) wherein L is chlorine or bromine or an activated hydroxy group, preferably a hydroxy group activated in the form of a reactive ester with a sulphonic acid, or in the form of a reactive complex obtained upon reaction with a trivalent organophosphorus compound, preferably triphenylphosphine, and an azo-dicarboxylic acid ester, preferably diethylazodicarboxylate; or
b) by reacting a compound of formula (II) wherein L is a free hydroxy group with a reactive derivative of a compound of formula (III) wherein Y is -S-Het, i.e. a complex between the disulfide thereof and a derivative of trivalent phosphorus, e.g. of the kind previously specified.
When in a compound of formula (II) or in a compound of formula (III) any group is present which may interfere in the displacement reaction of the group L by the substituent Y, such group is protected in a conventional manner before the reaction takes place and, if desired, it is removed at the end of the reaction in a conventional manner too.
Optional conversions of a compound of formula (I) into another compound of formula (I) include, for example, the removal of the protecting groups possibly present, e.g. hydroxy, mercapto, amino and carboxy protecting groups. The removal of the protecting groups may be carried out by known methods such as, for instance, hydrogenolysis, e.g. in the presence of palladium on charcoal as catalyst, or by hydrolysis, either acid hydrolysis, e.g. with acetic acid or oxalic acid, or neutral or basic hydrolysis, or hydrolysis under reductive conditions, for example by the use of Fe/NH4CI or of Na2S2O4.
The optional salification of a free compound of formula (I), the optional preparation of a free compound of formula (I) from a salt thereof, and the optional separation of a mixture of isomers of formula (I) into the single isomers may be carried out following the known and usual procedures of the organic chemistry.
The compounds of formula (II) wherein L is hydroxy are known compounds or may be prepared by known methods from known compounds; they may be also obtained, for example, according to the method described in our published British patent application 80 05476.
A compound of formula (II) wherein L is chlorine or bromine may be obtained, e.g., by reacting a compound of formula (II) wherein L is hydroxy with an appropriate halogenating agent which may be, for example, thionyl chloride, a phosphorous halide, phosphorous tribromide for instance, triphenylphosphine'carbontetrachloride or triphenylphosphine/carbon tetrabromide.
A compound of formula (II) wherein L is an activated hydroxy group may be prepared from a compound of formula (II) wherein L is a free hydroxy group by known and conventional procedures.
Thus, for example, a compound of formula (II) wherein L is a hydroxy group activated in the form of a reactive ester with a sulphonic or carboxylic acid may be obtained by reaction with the appropriate sulphonyl halide, preferably chloride or sulphonic anhydride, or, respectively, with the appropriate carboxylic acyl halide, preferably chloride, or anhydride.
Similarly a compound of formula (II) wherein L is a hydroxy group activated in the form of a reactive ester with a phosphoric acid may be prepared by reacting the corresponding formula (II) compound wherein L is hydroxy with an appropriate phosphorus halide, preferably chloride. The hereabove indicated transformations of a compound of formula (II) wherein L is a free hydroxy group into a compound of formula (II) wherein L is a hydroxy group activated in the form of a reactive ester are, preferably, performed in an anhydrous solvent such as for instance, tetrahydrofuran, dimethylformamide or a halogenated hydrocarbon, e.g. dichloromethane, optionally in the presence of a base, preferably an organic base such as, for example, triethylamine, pyridine or lutidine.
A compound of formula (II) wherein L is a hydroxy group activated in the form of a reactive complex or reactive acetal of the kind hereabove specified may be obtained by known standard procedures.
In many instances, the compound of formula (II) containing the activated hydroxy group is not actually isolated but is reacted in situ (that is in the same reaction mixture wherein it is obtained from the corresponding compound of formula (II) wherein L is a free hydroxy group) with the compound of formula (III) or the salt thereof: this usually occurs, for example, when a compound of formula (II) is used wherein the hydroxy group is activated in the form of a reactive complex or reactive acetal of the type described above in this specification.
The compounds of formula (III) are known compounds or may be prepared by known methods from known compounds. A reactive derivative of a compound of formula (III) as defined above may be obtained by known and standard procedure from a free compound of formula (III). Also the said reactive derivative of a compound of formula (III) is not, usually, isolated but is reacted in situ, i.e. in the same reaction mixture wherein it is obtained from the compound (III), with the compound of formula (II) wherein L is a free hydroxy group.
The compounds of formula II wherein L is a hydroxy group activated in the form of a reactive ester with a sulphonic acid are included in the scope of the present invention.
A further object of the invention are new compounds of the following formula (la)
wherein
R'1 is a C1-C6 alkyl group substituted by a free or protected hydroxy;
R2 is hydrogen or a carboxy protecting group; and
Y is
1) an optionally substituted pyridyl group; or
2) a group -S-alk-NH2 wherein alk represents a C1-C3 alkylene; or
3) a group -S-Het' wherein Het' represents:
a) 1,3,4-thiadiazolyl either unsubstituted or substituted by a substituent chosen from (a') C2-C6 alkyl; (b') C1-C3 alkyl substituted by an optionally salified carboxy group; (c') an optionally salified carboxymethylthio group; and (d') a group -N cg:. wherein each of R' and R" is, independently, hydrogen or C1-C3 alkyl;
b) 1,2,3-thiadiazolyl optionally substituted by a C1-C6 alkyl group;
c) 1,2,3-triazolyl substituted by a C1-C6 alkyl group;
d) 1,2,4-triazolvl optionally substituted by a group -N cR:. wherein R' and R" are as defined above;
e) 1,3,4-triazolyl optionally substituted by a C1-C6 alkyl group;
f) imidazolyl ootionally substituted by a C1-C6 alkyl group;
g) thiazolyl optionally substituted by one or more substituents chosen from (a') -N= R, wherein R' and R" are as defined above; (b') unsubstituted Cl-C6 alkyl; and (c') C1-C3 alkyl substituted by an optionally salified carboxy group;
h) tetrazolyl optionally substituted by (a') unsubstituted C1-C6 alkyl, or (b') C,-C3 alkyl substituted by a substituent chosen from (i) optionally salified carboxy, (ii) optionally salified sulpho or sulfoamino, (iii) cyano, (iv) carbamoyl, (v) -N = W:. wherein R' and R" are as defined above, and (vi) tetrazolyl;
i) pyrazinyl substituted by a Cl-C6 alkyl or Cl-C6 alkoxy group;
I) 5-oxo-6-hydroxy-2,5-dihydro-1 ,2,4-triazinyl and 5-oxo-6-hydroxy-4,5-dihydro-1,2,4-triazinyl both optionally substituted by a C1-C3 alkyl group; or
m) tetrazolo-pyridazinyl optionally substituted by (a') an optionally salified carboxy group or (b') a group -N 66:.wherein R' and R" are as defined above; provided that when Y' is a group -S-Het' wherein Het' is 1,2,3,4-tetrazol-5-yl substituted by C1-C6 alkyl at the 1-position, then R'1 is not ot -hydroxyisopropyl, and the pharmaceutically or veterinarily acceptable salts thereof.
In the above formula (la) a Cl-C6 alkyl group is, preferably methyl, ethyl, n-propyl, isopropyl or isobutyl; a C2-C6 alkyl group is, preferably ethyl or isopropyl; a CC2\alkyl group is, preferably, methyl or ethyl; a C1-C3 alkylene is, preferably, ethylene; a C1-C6 alkoxy group is, preferably, methoxy or ethoxy; a group -NR is, preferably, amino, monomethylamino or dimethylamino; a salified carboxy or sulpho group is, preferably, salified with an alkali metal, sodium in particular, and the protecting groups of the hydroxy and carboxy functions may be the same previously specified with reference to formula (I).Also the pharmaceutically or veterinarily acceptable salts of the compounds of formula (la) may be the same indicated above for the compounds of formula (I), and they include both the salts of the compounds of formula (la) wherein R2 is hydrogen and the salts of the compounds of formula (la) wherein Het' represents a salifiable heterocyclic ring or a heterocyclic ring containing a salifiable substituent, as well as the internal salts, i.e. zwitterions.
Preferred salts are those of the compounds of formula (la) wherein R2 is hydrogen with a pharmaceutically or veterinarily acceptable base, particularly an inorganic base such as, e.g., an alkali metal hydroxide, sodium hydroxide or potassium hydroxide for instance.
Preferably in the above formula (la) R'1 represents an a-hydroxyethyl, wherein the hydroxy group is either free or protected, for example by a p-nitro-benzyloxycarbonyl or a tert-butyldimethylsilyl group.
Preferably R2 is hydrogen, a cation or a carboxy protecting group chosen from alkyl, p-nitro-benzyl, tert-butyldiphenyl-silyl and acetoxymethyl.
When Y' is an optionally substituted pyridyl group it is, preferably, a 1-pyridyl group optionally substituted by a carbamoyl group, in particular 4-carbamoyl.
When Y' is a group -S-alk-NH2 as defined above, it is, preferably, a group -S-CH2-CH2-NH2.
When Y' is a group -S-Het', Het' preferably represents: 2-carboxymethyl-1,3,4-thiadiazol-5-yl ; 2-amino-1,3,4-thiadiazol-5-yl ; 5-carboxymethylthio-1 ,3,4-thiadiazol-2-yl; 2-amino-1,3-thiazol-5-yl ; 4-methyl-5-carboxymethyl-1,3-thiazol-2-yl ; tetrazol-5-yl; 1-methyl-1,2,3,4-tetrazol-5-yl ; 1 -ca rboxy-m ethyl-l ,2,3,4-tetrazol-5-yl; 1-carboxy-ethyl-1,2,3,4-tetrazol-5-yl ; i-cyano-methyl-i,2,3,4-tetrazol-5-yl; 1-cyano-ethyl-1,2,3,4-tetrazol-5-yl ; 1 -sulpho-methyl-1 ,2,3,4-tetrazol-5-yl; 1 -sulpho-ethyl-1 ,2,3,4-tetrazol-5-yl; 1 -dimethylaminomethyl-1 ,2,3,4-tetrazol-5-yl; 1 -dimethylaminoethyl-i ,2,3,4-tetrazol-5-yl; 1 -aminocarbonylmethyl-1 ,2,3,4-tetrazol-5-yl; 1 -(2-aminoca rbonyiethyl)-i ,2,3,4-tetrazol-5-yl; 6-methoxy-pyrazyn-2-yl; 5-oxo-6-hydroxy-2,5-dihydro-l ,2,4-triazin-3-yl; 5-oxo-6-hydroxy-4,5-dihydro-l ,2,4-triazin-3-yl; 1,2,3,4-tetrazolo[1,5-b]pyridazin-6-yl ; 8-amino-l ,2,3,4-tetrazoIo[l ,5-b]pyridazin-6-yl; or 8-carboxy-1,2,3,4-tetrazolo[1,5-b]pyridazin-6-yl.
Preferred compounds of formula (la) are those wherein R'1 is o-hydroxyethyl, with the hydroxy group optionally protected, R2 is hydrogen or a carboxy protecting group and Y' is a group -S-Het' wherein
Het' is one of the heterocyclic rings listed hereabove, and the pharmaceutically or veterinarily acceptable salts of these compounds, particularly the sodium and potassium salts.
Other preferred compounds of formula (la) are those wherein R'1 and R2 are as hereinbefore defined on this page and Y' is -S-CH2-CH2-NH2, and the pharmaceutically or veterinarily acceptable salts thereof.
All the possible isomers of formula (la), both geometrical and optical isomers, and their mixtures, and the metabolites and the metabolic precursors of the compounds of formula (la) are included in the scope of the present invention.
Preferred configuration for the compounds of formula (la) is the (5R, 6S) configuration and when, according to a particularly preferred feature, R'1 is an oc-hydroxyethyl group, the (5R, 6S, 8R) and (5R, 6R, 8S) configurations are the preferred ones, the (5R, 6S, 8R) configuration being most preferred.
Specific examples of preferred compounds of the invention are: (5R,6S)-6-[1(R)-hydroxyethyl]-2-[(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl]-thiomethyl]-penem-3-carboxylic acid ; (5B,6S)-6-(1 (B)-hydroxyethyl]-2-[(2-amino-1 3, 4-thiadiazol-5-yl)-thiomethyl]-penem-3-carboxylic acid; (5R,6S)-6-[1 (R)-hydroxyethyl]-2-[(5-carboxy-methylthio 1 ,3,4-thiadiazol-2-yl)-thiomethyl]-penem-3-carbox- ylic acid; (5R,6S)-6-[1 (R)-hydroxyethyl]-2-(1 ,2,3,4-tetrazol-5-yl) thiomethyl-penem-3-carboxylic acid; (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-[ 1 -(2-aminocarbonylethyl) 1 ,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-ca rboxylic acid;; (5R, 6S)-6-[1(R)-hydroxyethyl]-2-[2-cyanoethyl) -1,2,3,4-tetrazol-5-yl-thiomethyl-penem-3-carboxylic acid; (5R,6S)-6-[1(R)-hydroxyethyl]-2-[(5-carboxymethyl-1,3,4-thiadiazol-2-yl)-thiomethyl-penem-3-carboxylic acid; (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-[ 1 -(2-dimethylaminoethyl -1 ,2,3,4-tetrazol-5-yl )-th iomethyl-penem-3-ca r- boxylic acid; (5R,6S)-6-[1(R)-hydroxyethyl]-2-[(1-sulphomethyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylic acid; (5R, 6S)-6-[1 (B)-hyroxyethylj-2-[1 -(2-carboxyethyl)-1,2,3, 4-tetrazol-5-yl]-thiomethyl-penem-3-ca rboxyl i c acid; (5R,6S)-6-[1(R)-hydroxyethyl]-2-[(1-carboxymethyl)-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylic acid;; (5R,6S)-6-[1(R)-hydroxyethyl]-2-[(4-carboxymethyl-5-methyl-1,3-thiazol-2-yl)-thiomethyl-penem-3-carboxylic acid; (5R, 6S)-6-[1 (B)-hydroxyethyl]-2-(tetrazolo!1 ,5-b]pyridazin-6-yl)-thiomethyl-penem-3-carboxylic acid; (5R,6S)-6-[1(R)-hydroxyethyl]-2-[(8-carboxytetrazolo[1,5-b] pyridazin-6-yl)-thiomethyl-penem-3-carboxylic acid; (5R,6S)-6-[1(R)-hydroxyethyl]-2-(8-aminotetrazolo[1,5-blpyridazin-6-yl)-thiomethyl-penem-3-carboxylic acid; (5R,6S)-6-[1(R)-hydroxyethyl]-2-(6-methoxy-pyrazin-2-yl)-thiomethyl-penem-3-carboxylic acid ; (5R,6S)-6-[1(R)-hydroxyethyl]-2-(2-methyl-5-oxo-6-hydroxy-2,5-dihydro-1,2,4-triazin-3-yl)-thiomethyl-penem-3-carboxylic acid; (5R,6S)-6-[1(R)-hydroxyethyl]-2-(4-methyl-5-oxo-6-hydroxy-4,5-dihydro-1,2,4-triazin-3-yl)-thiomethyl-penem-3-carboxylic acid;; (5R, 6S)-6-[1 (R)-hyd roxyethyl]-2-(2-aminothiazol-5-yl) -thiomethyl-penem-3-carboxylic acid; and the pharmaceutically or veterinarily acceptable salts thereof, in particular the sodium and potassium salts. Another example of preferred compounds of the invention is (5R,6S) -6-[1(R)-hydroxyethyl]-2-(ss- aminoethyl)-thiomethyl-penem -3-carboxylic acid, and the pharmaceutically or veterinarily acceptable salts thereof.
The compounds of formula (la) may be prepared by the new process of the invention, involving the reaction between a compound of formula (II) and a compound of formula (lli). The compounds of formular (la) may also be prepared by a process comprising cyclizing a compound of formula (IV)
wherein R'1, R2 and Y' are as defined above and Ph is phenyl, and, if desired, converting an obtained compound of formula (la) into another and/or, if desired, salifying a free compound of formula (la) or obtaining a free compound of formula (la) from a salt thereof and/or, if desired, separating a mixture of isomers of formula (la) into the single isomers.
The cyclization of a compound of formula (IV) may be carried out by known conventional procedures, for example by heating in an inert solvent such as, for instance, an aromatic hydrocarbon like benzene or toluene, at temperatures varying from about 50 C to about 140 C, as reported, e.g. in our published British patent application 80 05476.
The optional conversion of a compound of formula (la) into another, such as, for example, the removal of possibly present protecting groups, the optional salification of a compound of formula (la) and the preparation of a free compound from a salt, as well as the optional separation of a mixture of isomers into the single isomers, may be carried out as reported above for the analogous transformations on the compounds of formula (I).
The compounds of formula (IV) may be prepared following known methods, e.g. as described in our published British patent application 80 05476.
The compounds of formula (I) and (la) have a high antibacterial activity both in animals and in humans against gram-positive and gram-negative bacteria such as staphylococci, streptococci, diplococci, Klebsiella, Escherichia coli, Proteus mirabilis, Salmonella, Shigella, Haemophilus and Neisseria. They show also a high activity against the strong beta-lactamase producer microorganisms, such as, for example, Klebsi e/la aerogenes 1082 E, Escherichia coli TEM, Enterobacter cloacae P 99, and indole-positive Proteus and the like, as well as against Pseudomonas aeruginosa strains.
For example, the compound (5R,6S)-6-[1 (R)-hydroxyethyl] -24tetrazolo[1 ,5-b]pyridazin-6-yl}4hiomethyl- penem -3-carboxylic acid was found to be particularly active against Gram-positive bacteria: in particular, for instance, minimal inhibiting concentrations of 0.002 ,ug/ml against Streptococcus pyogenes and pneumoniae and of 0.004 > giml against penicillinase producer and non-producer Staphylococcus aureus were found for the sodium salt of said compound.For the compound (5R,6S)-6-[1(R)-hydroxyethyl]-2-(2-methyl -5-oXo-6-hydroxy-2,5-dihydro-1,2,4-triazin-3-yl)-thiomethyl -penem-3-carboxylic acid disodium salt, for example, a particularly favourable activity was found against the Gram-negative bacteria such as, for instance Escherichia co/i 1507 E, Escherichia coli TEM, Klebsiella pneumoniae ATCC 10031 and Proteus vulgaris X 20.
Other examples of compounds for which particularly favourable values of minimal inhibiting concentrations were found both against Gram-positive and against Gram-negative bacteria are (5R, 6S)-6-[1(R) hydroxyethyi]-2-[1-(2-aminocarbonylethyl) -1 ,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-carboxylic acid, (5R, 6S)-6-[1 (R)-hydroxyethyll-2-(5-carboxymethylthio -1,3,4-thiadiazol-2-yl)-thiomethyl-penem-3-carboxylic acid and (5R, 6S)-6-[1 (R)-hydroxyethyll-2-[1-methyl-1,2,3,4tetrazol -5-yl)-thiomethyl]-penem-3-carboxylic acid.
Owing to their high antibacterial activity either in animals or in humans against both Gram-positive and Gram-negative bacteria the compounds of the present invention are useful in the treatment of the infections caused by said microorganisms, such as, respiratory tract infections, for example, bronchitis, bronchopneumonia, pleurisy; hepatobiliary and abdominal infections, for example, septicemia; urinary tract infections, for example, pyelonephritis, cystitis; obstetrical and gynecological infections, for instance, cervicitis, endometritis; ear, nose and throat infections, for instance, otitis, sinusitis, parotitis.
The toxicity of the compounds of the invention is quite negligible and therefore they can be safely used in therapy.
They may be administered, either to humans or to animals, in a variety of dosage forms, e.g., orally in the form of tablets, capsules, drops or syrups; rectally in the form of suppositories; parenterally, e.g., intravenously or intramuscularly (as solutions or suspensions), with intravenous administration being preferred in emergency situation; by inhalation in the form of aerosols or solutions for nebulizers; intravaginally in the form, e.g., of bougies; or topically in the form of lotions, creams and ointments. The pharmaceutical or veterinary compositions containing the compounds of the invention may be prepared in a conventional way by employing the conventional carriers or diluents used for, e.g., cephalosporins.
Conventional carriers or diluents are, for example, water, gelatine, lactose, starches, magnesium stearate, talc, vegetable oils, cellulose and the like. Daily doses in the range of about 1 to about 100 mg per kg of body weight may be used, in various animal species, the exact dose depending on the age, weight and condition of the subject to be treated and on the frequency and route of administration.
A preferred way of administration of the compounds of the invention is the parenteral one: in this case the compounds may be administered, for example to adult humans, in an amount ranging from about 100 mg to about 200 mg pro dose, preferably about 150 mg pro dose, 1-4 times a day, dissolved in a suitable solvent, such as, for example, sterile water or lidocaine hydrochloride solution for intramuscular injections, and sterile water, physiological saline solution, dextrose solution or the conventional intravenous fluids or electrolytes, for intravenous injections. Furthermore, the compounds of the invention may be used as antibacterial agents in a prophylactic manner, e.g., in cleaning or as surface disinfecting compositions, for example, at a concentration of about 0.2 to 1% by weight of such compounds admixed with, suspended or dissolved in conventional inert dry or aqueous carriers for application by washing or spraying. They are also useful as nutritional supplements in animal feeds.
The following Examples are given to illustrate the invention.
The abbreviations pNB, THF, EtOAc, TBDMS and TBDPS stand, respectively, for p-nitro-benzyl, tetrahydrofuran, ethyl-acetate, tert-butyldimethylsilyl and tert-butyldiphenylsilyl.
Example 1 p-Nitrobenzyl(5R, 6S)-6-(1(R)-hydroxyethyl]-2-nitrobenzyl-oxycarbonyloxymethyl-2-penem-3-carboxylate
To a solution of p-nitrobenzyl(5R, 6S)-6-[1 (B)-tert-butyl -dimethylsilyloxyethyl]-2-pnitrobenzyloxycarbonyloxymethyl -2-penem-3-carboxylate (950 mg, 1.41 mmol) in THF, acetic acid (806 ul, 14.1 mmol) and tetrabutylammonium fluoride trihydrate (1.33 g, 4.33 mmol) were added at 0"C with stirring.
The resulting solution was stirred for 22 hours at room temperature.
The organic solvent was removed under reduced pressure. The residue was dissolved in ethyl acetate, washed with 4% aqueous sodium bicarbonate, twice with brine, then dried over Na2SO4 and concentrated under reduced pressure
The residue was triturated in cyclohexane to give, after filtration of the solvent, white cristals (680 mg, 86%) of the title product.
UV (CHCl2) x,,= 325 nm
NMR (CDCI3) bppm 1.37 (3H, d, J=6.0Hz)
2.96(1H, b.s., exch, with D2O)
3.92 (IH, dd, J= 2.0 and 6.0 Hz)
4.26 (IH, m)
5.30 (2H, s)
5.35 (2H, ABq, J= 14 Hz, separation of inner lines = 14 Hz)
5.42 (2H, ABq, J= 13 Hz, separation of inner lines = 18 Hz)
5.68 (IH, d, J= 2.0 Hz)
7.56 (2H, d, J= 7.5 Hz)
7.61 (2H, d, J= 7.5 Hz)
8.20 (2H, d, J= 7.5 Hz)
8.23 (2H, d, J= 7.5 Hz)
Example 2 (5R, 6S)-6-[1 {R)-hydroxyethyll-2-hydroxymethyl-penem-3-carboxylic acid, sodium salt
To a solution of p-nitrobenzyl(5R, 6S)-6-[1 (B)-hydroxy ethyl]-2-(p-nitrobenzyloxycarbonyloxymethyl )-penem -3-carboxylate (750 mg, 1.34 mmol) in a mixture of ETOAc (25 ml) and water (25 ml), solid NaHCO2 (112 mg, 1.34 mmol) and 5% Pd/C (750 mg) were added. The two-phase mixture was hydrogenated under normal pressure for 1 hour.
A further amount of 5% Pd/C (750 mg) was then added and the hydrogenation was continued for 1 hour.
The mixture was then filtered and the organic phase was discarded. The aqueous phase was concentrated in vacuo to give a brownish oil which was purified on a reverse phase column eluting with water.
The title product was so obtained as an amorphous solid (210 mg, 61.2%).
UV (H2O) #max 259,306 nm
NMR (D2O) 8ppm 1.30 (3H, d, j= 7 Hz)
3.88 (1H, dd, J= 1 and 6.3 Hz)
4.23 (IH, m)
4.63 (2H ABq J= 14.5 Hz, separation of inner lines = 4 Hz)
5.62 (IH, d, J= 1 Hz)
Example 3 (5R, 6S)-6-[l {R)-tert-butyidimethylsilyloxyethyll-2 -h ydroxymeth yl-2-p en em-3-carboxylic acid
A solution of sodium bicarbonate (110 mg, 1.3 mmol) in water (25 ml) was added to a solution of pnitrobenzyl (5R, 6S)-6-[1 (R)-tert-butyldimethylsi lyloxyethyl]-2-p-nitrobenzyl oxycarbonyloxymethyl-penem3-carboxylate (875 mg, 1.3 mmol) in ethyl acetate (25 ml).
The mixture was hydrogenated over 5% palladium on charcoal catalyst (875 mg) for 2 hours.
A further amount of 5% palladium on charcoal (875 mg) was added and the mixture hydrogenated for four hours, After filtration through Hiflo filter aid, the aqueous phase was separated, concentrated in vacuo and the resulting residue was purified on a reverse phase column giving the sodium salt of the title compound as a while solid (252 mg, 52%).
An aqueous solution of the sodium salt was acidified with acetic acid and extracted with ethyl acetate.
The organic solvent was dried over sodium sulphate and evaporated under reduced pressure to give the free carboxylic acid as a light yellow foam.
UV (CHCl3) #max 324 nm IR (CHCI3) γmax 1785, 1710 cm 1
NMR (CDCI1) ppm 0.06 (3H, s)
0.90 (9H, s)
1.26 (3H, d, J= 6.0 Hz)
3.73 (lH, dd, J= 1.5, 5 Hz)
4.22 (lH, m)
4.67 (2H, s)
5.59 (lH, d, J= 1.5 Hz)
Example 4 p-Nitrobenzyl(5R, 6S)-6-(1(R)-tert-butyldimethylsilyloxy-ethyl]-2-hydroxymethyl-penem-3-carboxylate
A solution of p-nitrobenzyl(SB, 6S)-6-[1(R)-tert-butyl-dimethylsilyloxyethyol]-2-tert-butyldiphenylsilyloxy- methyl-penem-3-carboxylate (0.73 g, 1 mmol) in tetrahydrofuran (20 ml) was sequentially treated at +10"C with acetic acid (0.7 ml, 10 mmol) and tetrabutyl ammonium fluoride trihydrate (0.95 g, 3 mmoll, and the mixture stirred at the same temperature until most of the starting material had disappeared (TLC, 3 3 h).
The solvent was removed under vacuum and the residue was partitioned between ethyl acetate and aqueous sodium hydrogen carbonate. Evaporation of the organic phase, followed by chromatographic purification (SiO2, ethyl acetate-cyclohexane mixtures as eluants) afforded the title compound (345 mg, 70%) as a white foam.
NMR (CDCI3) #ppm 0.05 (6H, S)
0.85 (9H, s)
1.25 (3H, d)
3.44 (lH, t, exch. with D2O)
3.78 (lH, dd)
4.29 (lH, m)
4.64 (2H, d, collapses to a s after exch. with D2O)
5.32 (2H, ABq)
5.64 (1H, d)
7.60 (2H, d)
8.20 (2H, d)
Example 5 p-Nitrobenzyl(5R, 6S)-6-(1(R)-hydroxyethyl]-2-hydroxy-methyl-penem-3-carboxylate
A solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-tert-butyl-dimethylsilyloxyethyl]-2-tert-butyldiphenylsilyloxy- methyl -penem-3-carboxylate (0.93 g, 1 mmol) in tetrahydrofuran (20 ml) was stirred for 20 h at room temperature in the presence of acetic acid (1.14 ml, 20 mmol) and tetrabutyl-ammonium fluoride trihydrate (1.89 g, 6 mmoi). The solvent was removed in vacuo and the residue was partitioned between ethyl acetate and an aqueous solution of sodium hydrogen carbonate. The organic layer was washed with water, dried over Na2SO4 and evaporated to give a syrup which was purified by trituration in a small amount of dichloromethane. The title product was collected as a white-off powder (290 mg; 76%).
UV (EtOH) #max 264, 322 nm
IR γmax 3400-3200, 1780, 1690 cm-1 NMR (EtOH-6) #ppm 1.45 (3H, d, J= 6.5 Hz)
3.67 (1H, dd, J= 1.5, 6.0 Hz)
4.10 (1H, m)
4.72 (2H, s)
5.32 (2H, ABq, J= 14 Hz)
5.59 (1H, d, J= 1.5 Hz)
7.69 (2H, d, J= 7 Hz)
8.18 (2H, d, J= 7 Hz)
Example 6 p-Nitrobenzyl(5R, 6S)-6-(1(R)-p-nitrobenzyloxycarbonyloxyethyl)-2-hydroxymethyl-penem-3-carboxylate
Acetic acid (157 AI;; 2.76 mmol) and tetrabutylammonium fluoride trihydrate (261 mg, 0.87 mmol) were sequentially added to a solution of p-nitrobenzyl(5R, 6S)-6-[1-(R)-p-nitrobenzyloxycarbonyloxycthyl]-2-tert- butyldiphenyl-silyloxymethyl-penem-3-carboxylate (220 mg, 0.276 mmol) in tetrahydrofuran (10 ml) and the mixture was stirred for several hours at room temperature.
Work-up after 4-5 hours, as described in Example 1, afforded the title product as the major component.
Silica gel chromatography (EtOAc-cyclohexane mixtures) gave the pure material.
[al20 + 66 (1.3% in CHCI3) UV (CHCl3) #max 269 (e= 17.000) and 323 (e= 6.800) nm,
IR(film) wmax 1795, 1755 and 1710 cm--', NMR (CDCl3) #ppm 1.51 (3H, d, J= 6.5 Hz)
3.55 (1H, bs)
3.97 (1H, dd, J= 2.0 and 8.0 Hz)
4.68 (2H, s)
5.19 (1H, dq, J= 6.5 and 8.0 Hz)
5.25 -5.45 (4H, m)
5.65 (1H, d, J= 2.0 Hz)
7.4-8.5 (8H, m)
When the reaction was left running for a prolonged time (15 hours or more), an elimination product (E,
Z mixture) was collected as the major component::
IR (nujol) Amax 3550-3100, 1800, 1785-1760, 1705
and 1685 cm-l NMR (CDCI3) #ppm (Z)isomer: 1.95 (3H, t, J= 8.0 Hz)
4.65 (2H, s)
5.32 (2H, ABq, J= 14 Hz,
separation of inner
lines 6 Hz)
6.13 (1H, s)
6.46 (1H, q) (E)isomer: 2.15 (3H, t, J= 7.5 Hz)
4.65 (2H, s)
5.32 (2H, ABq, J= 14 Hz)
separation of inner
lines 6 Hz)
6.13 (1H, s)
6.20 (1H, dq)
Example 7 p-Nitrobenzylf5R, 6S)-6-11(RJ-hydroxyethylJ-2-hydroxy-methyl-penem-3-carboxylate
To a solution of p-nitrobenzyl(5R, 6S)-2-hydroxymethyl-6-[1(R)-tert-butyldimethylsilyloxyethyl]-penem-3- carboxylate (1.2 g, 2.4 mmol) in THF (50 ml) acetic acid (1.47 ml, 24 mmol) and tetrabutylammonium fluoride (2.27 g, 7.2 mmol) were added.
The resulting mixture was stirred at room temperature for 16 hours.
The solution was then evaporated in vacuo and the residue was chromatographed on silica gel eluting with ethyl acetatelcyclohexane mixtures to give the title product as a light yellow solid (775 mg, 85%).
UV (EtOH) Amax 264, 322
NMR (EtOH-d6) ),ppm 1.45 (3H, d, J= 6.5 Hz)
3.67 (1H, dd, J= 1.5, 6.0 Hz)
4.10 (1H, m)
4.72 (2H, s)
5.32 (2H, ABq, J= 14 Hz, separation of inner lines 8 Hz)
5.59 (1H, d, J= 1.5 Hz)
7.69 (2H, d, J= 7 Hz)
8.18 (2H, d, J= 7 Hz)
Example 8
Sodium (5R, 6SJ-6-[1rR)-hydroxyethyl7-2-hydroxymethyl-penem-3-carboxylate
A solution of p-nitrobenzyl(5R, 6S)-6-[1 (R)-hydroxyethyl]-2-hydroxymethyl-penem-3-carboxylate (450 mg, 1.2 mmol) in EtOAc (25 ml) and water (25 ml) containing NaHCO3 (100 mg, 1.2 mmol) was hydrogenated over 5% Pd/C (450 mg). The reaction was then carried out as described in Example 2. The title product was obtained as an amorphous solid (250 mg, 81%).
The product proved to be identical with the one obtained in Example 2.
Example 9
Sodium (5R, 6S)-6-(1(R)-hydroxyethyl]-2-hydroxymethyl-penem-3-carboxylate
A solution of p-nitrobenzyl(SB, 6S)-6-p[1(R)-p-nitrobenzyl-oxycarbonyloxyethyl]-penem-3-carboxylate (950 mg, 0.17 mmol) in EtOAc (25 ml) was hydrogenated as described in Example 2, thus obtaining the title compound as a solid (230 mg, 51.3%i.
This material proved to be identical with the compound obtained in Example 2.
Example 10
Diphenyl-tert-butylsilyl(5R, 6S)-6-(1(R)-hydroxyethyl]-2-hydroxymethyl-penem-3-carboxylate
A suspension of sodium(5R, 6S)-6-11(R)-hydroxyethyl] -2-hydroxymethyl-penem-3-carboxylate (108 mg, 0.4 mmol) in anhydrous THF (20 ml) was treated with tert-butyldiphenylsilylchloride (104 1, 0.4 mmolr.
The heterogeneous mixture was stirred for 2 hours at room temperature. The suspension was then filtered and the filtrate was evaporated in vacuo to give an oil which was purified on a silica gel column eluting with EtOAc/cyclohexane mixtures.
The title product was thus obtained as a colourless oil (150 mg, 77.4%)
UV (CHCl3) $man 328 nm
NMR (CDCI3) #ppm 1.11 (9H. s)
1.32 (3H, d, J= 6 Hz)
3.76 (IH, dd, J= 1.5, 6.0 Hz) 4.17 (1H, m)
4.53 (2H, s)
5.58 (1H, d, J= 1.5 Hz)
7.22 -7.90 (10H, m)
Example 11
Tert-butyldiphenylsilyl(5R, 6S)-6-[1(R)-hydroxyethyl]-2-methanesulphonyloxymethyl-penem-3-carboxylate
Triethylamine (45 l, 0.32 mmol) and methanesulphonyl chloride (25 l, 0.32 mmol) were sequentially added to a stirred solution of diphenyl-tert-butylsilyl(5R, 6S)-6-[1(R)-hydroxyethyl]-2-hydroxymethyl-penem-3-carboxylate (150 mg, 0.31 mmol) in cold (-30"C), anhydrous dichloromethane (5 ml). The progress of the reaction was monitored by TLC.
The reaction mixture was then washed with aqueous NaHCO3 solution and water. The organic phase was separated, dried over anhydrous Na2SO4, and evaporated in vacuo at a temperature below 10 C. The title product was thus obtained as an oil (150 mg, 86%).
UV (CHCl3) Am 329 nm
NMR (CDCl3) #ppm 1.10 (9H, s)
1.34 (3H, d, J= 6.5 Hz)
3.10 (3H, s)
3.81 (1H, dd, J= 1.5, 6.0 Hz) 4.21 11H, m)
5.17 (2H, ABq, J= 12 Hz, separation
of inner lines 16 Hz)
5.66 (1H, d, J= 1.5 Hz)
7.21 -7.85 (10H, m)
Example 12
Tert-butyldiphenylsilyl(5R, 6S)-[1(R)-hydroxymethyl]-2-[(1-methyl-1,2,3,4-tetrazol-5-yl)-thioethyl]-penem-3carboxylate
To a solution of tert-butyidiphenylsilyl(5R, 6S)-6-[1(R)-hydroxyethyl]-2-methanesulphonyloxymethyl-penem-3-carboxylate (150 mg, 0.27 mmol) in EtOAc (2 ml) a solution of 1-methyl -5-mercapto-1,2,3,4-tetrazole sodium salt (41.5 mg, 0.3 mmol) in anhydrous THF (5 ml) was added at -30"C with stirring.
The resulting mixture was let stand at -300C for 6 hours and then was evaporated in vacuo. The residue was taken up in EtOAc (5 ml) and carefully washed with aqueous NaHCO3 and water. The organic layer was dried over anhydrous Na2SO4 and evaporated in vacuo to give the title product as an oil (97 mg, 62%)
UV (CHCl3) #max 337 nm
NMR (CDCl3) $ppm 1.13 (9H, s)
1.34 (3H, d, J= 6.0 Hz)
3.82 (1H, dd, J= 2.0, 6.0 Hz)
3.85 (3H, s)
4.19 (1H, m)
4.6 (2H, ABq, J= 14 Hz, separation
of inner lines = 17 Hz)
5.61 (1H, d, J= 1.5 Hz)
7.24-7.83 (10H, m)
Example 13
Sodium (5R, 6S)-6-J1 (R)-hydroxyeth yl'-2-[(1-methyl- 1,2,3,4-tetrazo/-5-y/)-thiom ethy/]-penem-3-carboxy/a te
A solution of tert-butyidiphenylsilyl(5R, 6S)-6-[1(R)-hydroxyethyl]-2-[(1-methyl-1,2,3,4-tetrazol-5-yl)- thiomethyl]-penem-3-carboxylate (95 mg, 0.14 mmol) in THF (2 ml), H2O (2 ml) and acetic acid (1 ml) was stirred at room temperature for 2 hours. The solution was then evaporated in vacuo at a temperature below 10"C. The oily residue was taken up in 2% aqueous NaHCO3 (1 ml). The aqueous phase was washed with EtOAc and the organic phase was discarded. The aqueous phase was then passed through a reverse phase column. Elution with water yielded the title product as an amorphous solid (34 mg, 67%).
UV (H3O) A,, 315 nm
NMR (D2O) #ppm 1.28 (3H, d J= 6.3 Hz)
3.87 (1H, dd, J= 1.4 and 6.3 Hz)
4.10 (3H, s)
4.19 (1H, m)
4.40 (2H, ABq, J= 16.0 Hz, separ
ation of inner lines = 13 Hz) 5.59 (1H, d, J= 1.4 Hz)
Example 14
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-[(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl]-penem-3-carboxylate
Method A
A suspension of sodium (5R, 6S)-6-[1(R)-hydroxyethyll -2-hydroxymethyl-penem-3-carboxylate (100 mg, 0.37 mmol) in anhydrous THF (20 ml) was treated with tert-butyldiphenyl silyl chloride (96 1*1, 0.37 mmol).
The heterogeneous mixture was stirred for 2 hours at room temperature.
The suspension was filtered and the filtrate was cooled at - 30"C. Et3N (52 lli, 0.37 mmol) and methanesulphonyl chloride (29 ill, 0.37 mmol) were then added dropwise to this solution under stirring. After 30 minutes, the resulting mixture was partitioned between EtOAc and an aqueous NaHCO3 solution.
The organic phase was carefully washed with water, dried over anhydrous Na2SO4, filtered and cooled again at -30"C. A solution of 1-methyl--S-mercapto-1,2,3,4-tetrazole sodium salt (55.2 mg, 0.4 mmol) in
THF (10 ml) was then added. After 6 hours at -30"C the mixture was evaporated in vacuo and the residue was taken up in EtOAc and washed with water.
The dried organic phase was evaporated in vacuo and the oily residue dissolved in THF (2 ml). Acetic acid (1 ml) and water (2 ml) were added, the solution was stirred at room temperature for 2 hours and then evaporated in vacuo. The oily residue was taken up with 2% aqueous NaHCO3, washed with EtOAc and purified through a reverse phase column to give the title product, identical with the one described in
Example 13.
Method B
A suspension of sodium (5R, 6S)-6-[1 (B)-hydroxymethyl] -2-hydroxymethyl-penem-3-carboxylate (100 mg, 0.37 mmol) in anhydrous THF was treated with trimethylsilyl chloride (150 aI, 0.4 mmol). The heterogeneous mixture was stirred for 2 hours at room temperature. The suspension was then filtered and the filtrate was cooled at -30 C. Et3N (52 FI, 0.37 mmol) and methanesulphonyl chloride (29 iii, 0.37 mmol) were then added to the solution drop by drop with stirring, followed after half an hour by a THF solution of 1-methyl-5-mercapto-1,2,3,4 -tetrazole sodium salt (55.2 mg, 0.4 mmol).
The resulting mixture was stirred at -30"C for 6 hours, after which time was evapourated in vacuo to dryness. The residue was dissolved in water containing NaHCO3 and the solution was passed through a reverse phase column to yield the title product, which was found identical with the one obtained by the above method A.
Example 15 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-methylsulphonyloxymethyl-penem-3carboxylate
A solution of p-nitrobenzyl(SB, GS)-6-[1(R)-p-nitrobenzyl -oxycarbonyloxyethyll-2-hydroxymethyl-2-pe- nem-3-carboxylate (100 mg, 0.178 mmol) in gry dichloromethane (5 ml) was sequentially treated at -15"C with triethylamine (58 mg, 0.58 mmol) and methanesulphonylchloride (60 mg, 0.58 mmol). After 10 minutes the reaction mixture was washed with aqueous sodium bicarbonate and then with water. The dried (Na2SO4) organic phase was evaporated in vacuo to give the title product as a pale yellow syrup.
UV (CHCl3) A,,= 226, 325
NMR (CDCl3) #ppm 1.51 (3H, d, J= 7 Hz)
3.09 (3H, s)
4.02 (1H, dd, J= 2 and 7.5 Hz)
4.92 and 5.64 (2H, centres of ABq, J= 17 Hz)
5.16 (1H, m)
5.25 (2H, s)
5.27 and 5.51 (2H, centres of ABq, J= 15 Hz)
5.71 (1H, d, J= 2 Hz)
7.50 (2H, d, J= 8 Hz)
7.60(2H, d, J= 8 Hz)
8.20 (4H, two superimposing d, J= 8 Hz)
MS (FD) mle 637 (M' ). C2H23N3O,3S3requires M, 637
Example 16 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-[1-methyl-1,2,3,4-tetrazol-5-yl-thiome thyl]-penem-3-carborvlate
1-methyl-5-mercapto-tetrazole sodium salt bihydrate (52 mg, 0.3 mmol) was added in a single portion to a cold THF solution (20 ml) of the mesylate obtained in Example 15 (38 mg, 0.06 mmol).
After one hour at 0 C the reaction mixture was evaporated, and the residue chromatographed on silica gel eluting with cyclohexane/EtOAc mixture. The title product was thus obtained as a pale yellow syrup (29 mg, 75%).
UV (CHCl3) #max 266 and 330
NMR (CDCl3) #ppm 1.48 (3H, d, J= 7 Hz)
3.84 (1H, dd, J= 2 and 5.5 Hz)
3.96 (3H, s)
4.69 (2H, ABq, J= 14 Hz, separ
ation of inner lines 18 Hz)
5.20 (1H, m)
5.24 (2H, s)
5.27 (2H, ABq, J= 13 Hz, separ
ation of inner lines 20 Hz)
5.61 (1H, d J= 2 Hz)
7.51 (2H, d, J= 8 Hz)
7.82 (2H, d, J= 8 Hz)
8.02 (4H, two superimposing d, J= 8 Hz)
MS (FD) mle 657 (M'). C26H23N7O0S2requires M, 657
Example 17 p-Nitrobenzy/(5R, 6SJ-6= R)-p-nitrobenzyloxycarbonyloxy-ethyl]-2-p-tolyl sulphonyloxymethyl-penem-3carboxylate
To a stirred solution of p-nitrobenzyl(5R, 6S)-6-[1(R) -p-nitrobenzyloxycarbonyloxyethyl]-2-hydroxymethyl-penem -3-carboxylate (56 mg, 100 umol) in dichloromethane (2 ml) at 0 C, triethylamine (17 FI, 120 gmmol) and p-toluenesulphonyl chloride (21 mg, 110 mol) were sequentially added. The resulting solution was stirred at OC for 15 minutes. A further amount of triethylamine (10 l) and p-toluenesulphonyl chloride (13 mg) was added and the mixture was stirred for twenty minutes at 5 C.
After this time the organic solution was washed with a 4% aqueous sodium bicarbonate solution, then with brine. The organic phase was dried over Na2SO4 and concentrated in vacuo.
Chromatography of the residue on silica gel (elution with hexane/ethyl acetate mixtures) gave a light yellow oil (42 mg, 79%).
UV (CHCl3) A,,, 267, 327
1R(film) #max 1795, 1750, 1710 cm
NMR (CDCI3) #ppm 1.50 (3H, d, J= 6.0 Hz)
2.47 (3H, s)
3.82 (1H, dd, J= 2.0, 6.0 Hz)
5.00 -5.55 (4H, 2ABq)
5.19 (1H, m)
5.31 (2H, s)
5.63 (1H, d, J= 2 Hz)
7.27-7.82 (8H, m)
8.22 (4H, d, J= 8 Hz)
Example 18 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxy-ethyl)-2-(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylate
A solution of p-nitrobenzyl(5R, 6S)-6-[1(R) -p-nitrobenzyl-oxycarbonyloxyethyl]-2-p-tolylsulphonylOxy- methyl -penem-3-carboxylate (42 mg, 0.059 mmol) in tetrahydrofuran was treated with 1-methyl-5-mercapto-1,2,3,4-tetrazole sodium salt bihydrate (52 mg, 0.3 mmoll. The mixture was stirred for 3 hours at room temperature, the solvent was concentrated under vacuum and the residue partitioned between
EtOAc and aqueous NaHCO3.
The organic phase was dried (Na2SO4) and evaporated to give a crude which was purified through a silica gel column (EtOAc/C6Hl2), thus affording 26 mg (68%) of the title product, identical in every respect with the sample described in Example 16.
Example 19 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxy-ethyl)-2-chloromethyl-penem-3-carboxylate
To a solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxywarbonyloxyethyl]-2-hydroxymethyl-pe- nem-3-carboxylate (210 mg, 0.376 mmol) in methylene chloride (6 ml) and carbon tetrachloride (6 ml), triphenylphosphine (108 mg, 0.412 mmol) was added.
The solution was stirred for thirty hours at room temperature.
Evaporation of the organic solvent and purification of the residue by column chromatography (silica gel, elution with cyclohexane ethyl acetate mixtures) gave the title compound as a light yellow oil (168 mg, 77%).
UV (CHCl2) A,,, 267, 329 NMR (CDC13) #ppm 1.50 (3H, d)
4.00 (1H, dd, J= 2.0 and 7.0 Hz)
4.75 (2H, ABq, J= -13.5 Hz, separ
ation of inner lines = 13 Hz)
5.20 (1H, m)
5.35 (2H, ABq, J= 14 Hz, separ
ation of inner lines = 8 Hz)
5.26 (2H, s)
5.68 (lH, d, J= 2 Hz)
7.52 (2H, d, J= 8 Hz)
7.62 (2H, d, J= 8 Hz)
8.20 (4H, d, J= 8 Hz)
Example 20 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxy-ethyl]-2-[(1-methyl-1,2,3,4-tetrazol-5-yl)-thiome thyll-penem -3-carboxy/ate
p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-chloromethyl-penem-3-carboxylate (150 mg, 0.26 mmol) was dissolved in tetrahydrofuran (5 ml) at 0 C. 1-methyl-S-mercapto-1,2,3,4-tetrazole sodium salt bihydrate (31.3 mg, 0.18 mmol) was added and the resulting solution was stirred for an hour at 0 C and 2 hours at 25"C. The organic solvent was removed under reduced pressure and the residue chromatographed over silica gel eluting with toluene-ethyl acetate mixtures.
Title compound was obtained as a white foam (152 mg, 89%)
UV (CHIC13) A,, 266, 330
NMR (CDCI3) appm 1.48 (3H, d, J= Hz)
3.84 (1H, dd, J= 2.0 and 5.5 Hz)
3.96 (3H, s)
4.69 (2H, ABq, J= 14 Hz, separ
ation of inner lines = 18 Hz)
5.20 (1H, m)
5.24 (2H, s)
5.27 (2H, ABq, J= 13 Hz, separ
ation of inner lines = 20 Hz)
5.61 (1H, d, J= 2.0 Hz)
7.51 (2H, d, J= 8.0 Hz)
7.82 (2H, d, J= 8.0 Hz)
8.02 (4H, d, J= 8.0 Hz)
Example 21 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxy-ethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylate
A solution of diethylazodicarboxylate (21.6 jli; 0.137 mmol) and triphenylphosphine (36 mg, 0.137 mmol) in tetrahydrofuran (1.5 ml) was stirred at 0"C for thirty minutes.To this mixture a solution of p nitro benzyl (5R, 6S, 8R)-6-(1 -p-nitrobenzyloxycarbonyloxyethyl )-2-hydroxymethyl-penem-3-carboxyiate (76.5 mg, 0.137 mmol) and 1-methyl-5-mercapto-1,2,3,4-tetrazole sodium salt (18.9 mg, 0.137 mmol) in tetrahydrofuran (1.0 ml) was added dropwise at 0"C.
The resulting solution was stirred at 0"C for ten minutes, then concentrated in vacuo and purified by preparative layer chromatography to give the title compound as a white foam (61 mg, 68%).
This material shared the same spectroscopical properties with the sample previously described'in Example 20.
Example 22 p-nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxymethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)-thiome thyl-penem -3-carboxylate
A solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-nitrobenzyloxycarbonyloxyethyl]-2-hydroxymethyl-penem-3- carboxylate (300 mg, 0.536 mmol) in acetonitrile (10 ml) was treated with anhydrous 1-methyl-5-mer capto-1 2,3,4-tetrazole and dimethylformamide dineopentyl acetal (1.07 mmol each).
After stirring for 3 hours at room temperature, the solvent was removed in vacuo and the residue chromatographed on silica gel to give the title product in low yield.
IR (CH2CI2) #max 1795, 1755,1710 The product shared the same NMR and UV spectra with the sample obtained as described in Example 20.
Example 23
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-[( 1-methyl- 1,2,3, 4-tetrazo/-5-y/)-thiometh y/]-penem-3-carb oxy/ate
To a solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-[(1-methyl-1,2,3,4-te- trazol-5-yl)-thiomethyl]-penem-3-carboxylate (100 mg, 0.15 mmol) in THF (1.5 ml) an aqueous 1 M solution of NH4CI (7.5 ml) and iron powder (0.25 g) were added at 0 > C under vigorous stirring.
After 20 minutes a further amount of 1 M aqueous ammonium chloride solution (5 ml) and iron powder (1.1 g) were added and stirring was continued for 45 minutes.
The mixture was filtered and the filtrate was washed with Et2O (2 x 30 ml). The organic layer was discarded and the aqueous phase was evaporated in vacuo to dryness.
The residue was purified on a reverse phase column eluting with water to obtain (5R, 6S)-6-11(R)-hy- droxyethyl]-2-[ (1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl]-penem-3-carboxylic acid (20 mg), which, by treatment with a molar equivalent amount of sodium hydrogen carbonate and vacuum-drying, was converted into the corresponding sodium salt, identical with the sample obtained in Example 13.
Example 24 p-Nitrobenzyl(5R, 6S)-6-[1(R)-hydroxyethyl]-2-methyl-sulphonyloxymethyl-penem-3-carboxylate
A solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-hydroxyethyl] -2-hydroxymethyl-penem-3-carboxylate (100 mg, 0.27 mmol) in a mixture of CH2CI2 (4 ml) and THF (1 ml) was treated at 0C under stirring with Et3N (56 FLI, 0.4 mmol) and methanesulphonyl chloride (23 wi, 0.3 mmol) until complete reaction was achieved (TLC monitoring).
The solution was diluted with aqueous NaHCO3 and carefully washed with water.
The aqueous phase was discarded and the dried organic phase was evaporated in vacuo to give the title product as a yellow oil.
NMR (CDCl3) âppm 1.45 (3H, d, J= 6.5 Hz)
3.11 (3H, s)
3.84 (1H, dd, J= 1.5, 6.1 Hz)
4.25 (1H, m)
5.33 (2H, ABq, J= 12 Hz, separation
of inner lines = 10 Hz)
5.38 (2H, ABq, J= 14 Hz, separation
of inner lines 24 Hz)
5.75 (1H, d, J= 1.5 Hz)
7.61 (2H, d, J= 8 Hz)
8.02 (2H, d, J= 8 Hz)
Example 25 p-Nitrobenzyl(5R, 6S)-6-[1(R) hydroxyethyl]-2-[(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl]-penem-3-carbox plate
To a solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-hydroxyethyll-2-methylsulphonyloxymethyl-penem-3-car- boxylate (70 mg, 0.154 mmol) in ethyl acetate (2 ml), a solution of 1-methyl -S-mercapto-1,2,3,4-tetrazole sodium salt bihydrate (53. 6 mg, 0.3 mmol) in THF (5 ml) was added at -70"C under stirring.
After 1 hour the reaction mixture was let rise to -20 C and stirred overnight at -20"C.
The solution was then evaporated in vacuo. The resulting solid residue was taken up in ethyl acetate and washed with an aqueous solution of NaHCO3
The organic phase was separated, dried over an hydros Na2SO4, filtered and evaporated in vacuo to give a yellow oil which was purified by column chromatography eluting with ethyl acetate cyclohexane mixtures.
The title compound was so obtained as a colourless oil (40 mg, 30% overall yield based upon the 2hydroxymethyl intermediate).
UV (CHIC13) A,,, 255, 334 nm
NMR (CDCI3) #ppm 1.38 (3H, d, J= 6 Hz)
3.77 (1H, dd, J= 1.0 and 6.0 Hz)
3.93 (3H, s)
4.27 (2H, ABq, J= 15 Hz, separation
of inner lines = 16 Hz)
4.77 (2H, ABq, J= 15 Hz, separation
of inner lines = 16 Hz)
5.30 (2H, s)
5.33 (2H, ABq, J= 14 Hz, separation
of inner lines = 9 Hz)
5.64 (1H, d, J= 2.0 Hz)
7.56 (2H, d, J= 8 Hz)
8.22 (2H, d, J= 8 Hz)
Example 26
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylate
An aqueous 1 M solution of NH4CI (2 ml) and iron powder (0.1 g) were added to a THF solution of pnitrobenzyl (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylate (40 mg, 0.083 mmol).The mixture was vigorously stirred for 30 minutes at room temperature, after which time a further amount of the reactants, if required (TLC monitoring), was added, When the starting material had disappeared, the mixture was filtered, the filtrate washed carbonate and freeze-drying, as a white amorphous solid (18 mg, 59%).
Example 27
Tert-butyldiphenylsilyl(5R, 6S)-6-[1(R)-tert-butyldimethylsilyloxyethyl]-2-hydroxymethyl-penem-3-carboxylate
Sodium salt of (5R, 6S)-6-[1 (R)-tert-butyldimethylsilyloxyethyl]-2-hydroxymethyl-penem-3-carboxylic acid (30 mg, 78.6 mmol) was suspended in anhydrous tetrahydrofuran (4 ml).
Tert-butyldiphenylsilylchloride (20.1 ijI, 78.6 mmol) was added at room temperature.
After thirty minutes stirring, triethylamine (5.5 l, 39.3 mmol) and a further amount of tert-butyldiphenylsi!yl-chloride (10 FI, 39.3 mmol) were added. Within half an hour, the precipitate was completely dissolved. the solution was concentrated and the residue chromatographed over silica gel eluting with cyclohexane-ethy! acetate mixtures to give a colourless oil (30 mg, 64%).
UV (CHCl3) A,, 331
IR (CH)Cl2) #max 1790; 1710 cm 1
NMR (CDC13) 8ppm 0.07 and 0.08 (3H, two s)
0.88 (9H, s)
1.10 (9H, s)
1.24 (3H, d, J= 6.0 Hz)
3.50 (1H, t, exch. with D2O)
3.77 (1H, dd, J= 1.5 and 5.0 Hz)
4.24 (1H, m)
4.42 (2H, d, singlet after exch. with D20)
5.63 (1H, d, J= 1.5 Hz) 7.2-7.8 (10H, m)
Example 28
Tert-butyldiphenylsilyl(5R, 6S)-6-[1(R)-tert-butyldimethylsilyloxyethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)thiomethylpenem-3-carboxylate
To an ice cooled solution of tert-butyidiphenylsilyl(5R, 6S) -6-[1(R)-tert-butyldimethylsilyloxyethyl]-2-hy- droxy-methyl -penem-3-carboxylate (47 mg, 78.6 mmol) in dry tetrahydrofuran (4.5 ml) triethylamine (11 iii, 78.6 mmol) and methanesulphonyl chloride (6.1 pI, 78.6 mmol) were added. The solution was stirred for ten minutes at 0 C, then 1-methyl-5-mercapto -1,2,3,4-tetrazole sodium salt bihydrate (27.4 mg, 157.2 mmol) was added in a single portion. The resulting mixture was stirred at 0 C for seventy five minutes.
The residue obtained after evaporation of the solvent was purified by column chromatography (silica gel column, elution with cyclohexane-ethyl acetate mixtures) to give the title compound as a white foam (34 mg, 60%).
UV (CHCI3) A,, 338
This product was directly used for the next step (double desilylation).
Example 29
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylate
A solution of tert-butyldip henylsilyl(5R, 6S)-6-t1 (R)-tert -butyidimethylsilyloxyethyl]-2-(1-methyl-1,2,3, 4 tetrazol-5-yl)-thiomethyl-penem-3-carboxylate (34 mg, 0.049 mmol) in tetrahydrofuran (15 ml) was treated with 50% aqueous acetic acid (10 ml). The mixture was stirred for 20 hours at room temperature and then evaporated to dryness in vacuo. The residue was taken up in ice-cold distilled water (1 ml) and sodium hydrogen carbonate was added with stirring to bring the pH to 7.5. The solution was washed with ethyl acetate and then passed through a reverse phase column (LiChroprep.RP-18 Merck) to give the title product as an amorphous solid (4 mg, 22%).
Example 30
Acetoxymethyl(5R, 6S)-6-[1(R)-tert-butyldimethylsilyloxyethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethylpenem-3-carboxylate
Diethylazodicarboxylate (216 lli, 0.137 mmol) was added to a stirred solution of triphenylphosphine (36 mg, 0.137 mmol) in tetrahydrofuran (0.5 ml) at 0"C.
The mixture was stirred at 0"C for 30 minutes, then added to a solution of acetoxymethyl (R, 6S)-6 [1(R)-tert-butyl-dimethylsilyloxyethyl]-2-hydroxymethyl-2-oeben-3-carboxy-late (59 mg, 0.137 mmol) and 1-methyl-5-mercapto-1,2,3,4-tetrazole sodium salt (18.9 mg, 0.137 mmol) in tetra-hydrofuran (2 ml) at 0"C.
The mixture was stirred at 0 C for fifteen minutes.
The resulting solution was concentrated under reduced pressure and then purified by column chromatography (silica gel, elution with hexane-ethyl acetate mixtures) to give the title compound as a white foam (38 mg, 58%).
UV (CHC13) A,,,, 335
1R (CHCl3) #max 1785, 1760, 1720 cm
NMR (CDC13) Gppm 0.05 (6H, s)
0.87 (9H, s)
1.19 (3H, d, J= 6.0 Hz)
2.18 (3H, s)
3.68 (1H, dd, J= 2.0 and 4.0 Hz)
3.92 (3H,.s) 4.21 (1H, m)
4.72 (2H, ABq, J= 14.5 Hz, separation
of inner lines = 15 Hz)
5.54 (1H, d, J= 2.0 Hz)
5.92 (2H, ABq, J= 6.0 Hz, separation
of inner lines = 1 Hz)
Example 31 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-acetoxymethyl-penem-3-carboxylate
A solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyl -oxyca rbonyloxyethyl]-2-hydroxymethyl-penem- 3-carboxylate (350 mg, 0.58 mmol) in dry CH2CI2 (5 ml) was sequentially treated with pyridine (140 mg) and acetic anhydride (80 mg) an then stirred at room temperature for six hours. The mixture was washed with aqueous NaHCOa (3 x 5 ml) and water (1 x 5 ml). The dried (Na2SO,) organic phase was evaporated and the oily residue was purified by silica gel chromatography (eluent: cyclohexane-ethyl acetate) to give the title product as a syrup (200 mg).
UV (EtOH 95%) #max 265 and 321
IR (CHCI3) y 1795, 1750, 1715, 1610 and 1585 cm
NMR (CDCl3) #ppm 1.50 (3H, d, J= 7 Hz)
2.11 (3H, s)
4.01 (1H, dd, J= 1.8 and 7.5 Hz)
5.11 and 5.50 (2H, centres of ABq, J= 14 Hz)
5.15 (1H, m)
5.24 and 5.38 (2H, centres of ABq, J= 12 Hz)
5.28 (2H, s)
5.70 (1H, d, J= 1.8Hz) 7.55 (2H, d, J= 8 Hz)
7.64 (2H, d, J= 8 Hz)
8.22 (4H, d, two superimposing d, J= 8 Hz)
Example 32
Sodium (5R, 6S)-6-[1(R)-hydroxycthyl]-2-acetoxymethyl-penem-3-carboxylate
5% of Pd/C (0.8 g) was added to a solution of p-nitrobenzyl (5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonylox- yethyl)-2-acetoxymethyl -penem-3-carboxylate (850 mg) in a mixture of ethyl acetate (20 ml) and water (20 ml) containing sodium bicarbonate (100 mg). The mixture was hydrogenated at atmospheric pressure for one hour. A second portion of the catalyst (0.4 g) was then added and the hydrogenation carried on for another 30 minutes. The mixture was filtered, the aqueous phase was washed with ethyl acetate, concentrated at room temperature under vacuum and then passed through a reverse phase column eluting with water. The title compound was thus obtained as an amorphous solid (250 mg).
Elemental analysis Found: C, 40.62; H, 4.14; N, 4.29%
C11H12NO6SNa,H2O requires C,
40.36; H, 4.31; N, 4.27%
NMR (D2O) 3ppml.31 (3H, d, J= 6.5 Hz)
2.14 (3H, s)
3.94 (1H, dd, J= 1.4 and 6.4 Hz)
4.26 (1H, m)
5.28 (2H, ABq, J= 14.4 Hz, separation of inner lines = 17.6 Hz)
5.68 (1H, d, J= 1.4 Hz)
Example 33
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylate
A solution of sodium (5R, 6S)-6-[1(R)-hydroxyethyll-2-acetoxymethyl-penem-3-carboxylate (10 mg, 0.032 mmol) in dry acetonitrile (1 ml) was treated with anhydrous 1-methyl-5-mercapto-1,2,3,4-tetrazole (4.5 mg, 0.04 mmol) followed by acetic acid (1,8 l, 0.032 mmol). The mixture was refluxed for 90 minutes, then evaporated in vacuo, taken up in distilled water, brought to pH 7.5 with NaHCO3 and fractionated twice on a reverse phase column, eluting with water.
The fractions containing the title product were lyophilized to afford 1.5 mg (12%) of the title product, which displayed the same spectroscopical properties of the sample obtained from Example 13. A fairly iarge amount of the starting 2-acetoxymethyl -penem was recovered in the fractions following the product.
Example 34 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-acetoacetoxymethyl-penem-3-carboxylate
To a solution of p-nitrobenzyl(5R, 6S)-6-[1 (B)-nitro benzyloxycarbonyloxyethyl]-2-hydroxymethyl-pe- nem-3-carboxylate (420 mg, 0.7 mmol) in dry CH2Cl2 (5 ml), triethylamine (0.05 ml, 0.35 mmol) and diketene (0.02 ml, 1.5 mmol) were sequentially added. After stirring for 1 hour at room temperature, the solution was evaporated in vacuo to leave a brown oil which was taken up with ethyl acetate and washed with water.
The organic layer was separated, dried with anhydrous Na2SO4 and evaporated in vacuo again. The oily residue was chromatographed on silica gel eluting with cyclohexane -ethylacetate mixtures. The title product was so obtained as a colourless oil (260 mg, 55%) UV (CHCl3) A,,, 265, 317
IR (CHC13) #max 1795, 1750, 1720, 1605, 1580 cm
NMR (CDCl3) #ppm 1.52 (3H, d, J= 6.5 Hz)
2.31 (3H, s)
3.59 (2H, s)
4.06 (1H, dd, J= 2 and 6.5 Hz) 5.04-5.70 (5H, m)
5.51 (2H, s)
5.73 (1H, d, J= 2 Hz)
7.55 (2H, d, J= 8 Hz)
7.64 (2H, d, J= 8 Hz)
8.20 (4H, two superimposing d, J= 8 Hz)
Example 35
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-acetoacetoxymethylpenem-3-carboxylate
To a solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-acetoacetoxymethyl- penem-3-carboxylate (250 mg) in ethyl acetate (10 ml), an aqueous solution of sodium bicarbonate (30.9 mg in 10 ml) and 5% Pd/C (200 mg) were added. The resulting mixture was hydrogenated at atmospheric pressure for 1 hour. After this time another portion of the catalyst (100 mg) was added and the reaction carried on until hydrogen was no longer absorbed. The catalyst was filtered, the aqueous phase was separated and washed with ethyl acetate.
The organic phase was discarded and the aqueous phase was evaporated in vacua. The residue was purified through a reverse phase column eluting with water. The aqueous solution was evaporated leaving the title product as an amorphous solid (40 mg).
Uv (EtOH 95%) #max 260 nm ("4630), 305 nm (4890)
NMR (D2O) #ppm 1.29 (3H, d, J= 6.5 Hz)
2.32 (3H, s)
3.92 (1H, dd, J= 1.5, 6.0 Hz)
4.24 (1H, m)
5.15 -5.53 (2H, centres of ABq, J= 15 Hz)
5.65 (1H, d, H= 1.5Hz) Example 36
Sodium (5R, RS)-6-[1(R)-hydroxyethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylate
l-Methyl-5-mercapto-1,2,3,4-tetrazole sodium salt dihydrate (45 mg, 0.3 mmol) was added to a buffered (pH 6.8) aqueous solution of sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-aceto -acetoxymethyl-penem-3-carboxylate (35 mg, 0.1 mmol).
The solution was heated under nitrogen for 30 minutes at 52"C, to give a crude mixture of the unreacted starting materials and of the title product, which was fractionated on a reverse phase column (LiChroprep. RP-18 Merck) eluting with water.
Example 37 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-[1(2-aminocarbonylethyl)-1,2,3,4-tetra zo/-5-yl] -thiomethyl-penem-3-carboxylate
To a solution of p-nitrobenzyl (5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-mesyloxymethyl-2- penem-3-carboxylate (38 mg, 0.06 mmol) in dry THF (5 ml), 1-(2-amino-carbonylethyl)-5-mercaptotetra- zole triethylammonium salt (80 mg, 0.3 mmol) was added at room temperature. After half an hour the reaction mixture was evaporated in vacuo. The residue was chromatographed on silica gel eluting with cyclohexane-ethyl acetate mixture yielding the title product as a syrup.
UV (CHC13) A,,,, 266 and 332
IR (CHCl3) y,,,,, 3500, 3400, 1795, 1750, 1710 -1695, 1605 cm NMR (CDCI3) #ppm 1.47 (3H, d, J= 7 Hz)
2.7 (2H, t, J= 7 Hz)
3.83 (1H, dd, J=2 and 5.5 Hz) 4.3-5.0 (4H, m)
5.2 (1H, m)
5.25 (2H, s)
5.3 (2H, center of Abq)
5.62 (1H, d, J= 2 Hz)
7.5 and 7.81 (each 2H, d, J= 8 Hz)
8.0 (4H, two superimposing d, J= 8Hz)
MS (FD) mle 714 (M). C28H26N8OllS2 requires M, 714
Example 38
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1-(2-aminocarbonylethyl)-1,2,3,4-tetrazol-5-yl]-thiomethyl-penem3-carboxylate
A solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-[(2-aminocarbonylethyl)- 1,2,3, 4-tetrazol-5-yl]-thiomethyl-penem-3-carboxylate (100 mg, 0.14 mmol) in acetonitrile (5 ml) was treated with solution of Na2S204 (73 nig, 0.42 mmol) and NaHCO3 in distilled water (4.2 ml).
The mixture was stirred at room temperature with TLC monitoring. When the reaction was almost completed the solvent was evaporated in vacuo, the aqueous solution washed with ethyl acetate and then passed throu-gh a reverse phase column to afford the title product.
UV(H2O) h315 iim IR (KBrl y3400, 1770 and 1695 and 1610 cm
MS (FD) m/e (free acid) 400 (M'l. C13H16 N6O5S2 requires M,400.
By proceeding analogously, sodium (5R, 6S)-6-[1(R)-hydroxy -ethyl]-2-[1-(2-aminocarbonylmethyl)- 1,2,3,4-tetrazol -5-yl]-thiomethyl-penem-3-carboxylate was obtained.
Example 39
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(5-methyl-1,3,4-thiadiozol-2-yl)-thiomethyl-penem-3-carboxylate
Tert-butyldiphenylsilyl chloride (0.1 ml) was added to a suspension of sodium (5R, 6S)-6-11(R)-hydroxy- ethyl]-2-hydroxymethyl-penem-3-carboxylate (100 mg) in an hydros tetrahydroruran. After stirring for 2 hours at room temperature the undissolved matter was filtered off and the filtrate, cooled at -30 C, was treated with methanesulphonyl chloride (0.03 ml) followed, after 30', by a solution of 5-methyl-2-mercapto-1,3,4-thiadiazole sodium salt (60 mg) in tetrahydrofuran.
The mixture was kept overnight at -30 C, then evaporated in vacua, partitioned between EtOAc and water, and the organic phase evaporated again to give the crude tert-butyldiphenylsilyl ester of the title product. Desilylation with aqueous acetic acid and purification as described in Example 14 gave the final compound as an amorphous solid.
UV (H5O) A,,,, 314
NMR (D2O) 8ppm 1.37 (3H, dl
2.77 (3H, s)
3.87 (1H, dd)
4.30 (1H, m)
4.62 (2H, ABq)
5.62 (1H, d)
Example 40 p-nitrobenzyl(5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1-(2-cyano-ethyl)-1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3carboxylate
p-Nitrobenzyl(5R, 6S)-6-[1(R)-hydroxyethyl]-2-hydroxy-methyl-penem-3-carboxylate (37 mg, 0.1 mmol) was added to a stirred solution of N, N-diisopropylethylamine (35 ,LI, 0.2 mmol) in dry dichloromethane (1 ml).Trifluoromethane sulphonic anhydride (25 lli, 0.15 mmol) was then added, the mixture was stirred 20 min at room temperature, cooled in an ice-bath and treated with a further amount of diisopropylethylamine (26 l, 0.15 mmol), immediately followed by S-mercapto-1-(2-cyanoethyll-1,2,3,4-tetrazole (23 mg, 0.15 mmol). After 2 hours at 0 C ethyl acetate (10 ml) was added, and the resulting solution was sequentially washed with water, 5% aqueous solution of citric acid and 5% aqueous solution of sodium hydrogen carbonate. The organic layer was dried over Na2SO4, concentrated in vacuo and the residue was fractionated by silica gel chromatography (ethyl acetate-cyclohexane mixture) to yield the title compound (35 mg, 68%) as a foam.
IR (CHCl3l wmaX 2240, 1795, 1755, 1710 cm
NMR (CDCl3) #ppm 1.37 (3H, d, J= 7 Hz)
3.20 (2H, t, J= 7 Hz)
3.77 (1H, dd, J= 2 and 6 Hz)
4.30 (1H, m)
4.62 (2H, t, J= 7 Hz)
4.8 (2H, ABq, J= 15 Hz)
5.30 (4H, s + ABq)
5.65 (1H, d, J= Hz)
7.6 and 8.23 (each 2H, d, J= 8 Hz)
Example 41
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1-(2-cyanoethyl)-1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-carboxylate
p-Nitrobenzyl(5R, 6S)-[1(R)-hydroxyethyl]-2-[1-(2-cyanoethyl)-1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3carboxylate (35 mg, 0.068 mmol) dissolved in tetrahydrofuran (15 ml) was treated with 1M aqueous
NH4CI (1.5 ml) and iron powder (0.1 g) under vigorous stirring.After 30 min., the filtrate was evaporated in vacuo and passed through a reverse phase column eluting with water, thus obtaining 12 mg (45%) of the free acid corrsponding to the title product.
MS (FD) m/e 382(M'). C3H14N,O4S2 requires M, 382.
Treatment of the free acid with a molar equivalent amount of sodium hydrogen carbonate and freezedrying afforded the corresponding sodium salt [UV(H2O)#max 315 nm].
By preceeding analogously, sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1-(2-cyanomethyl)-1,2,3,4-tetrazol- 5-yl]-thiomethyl-penem-3-carboxylate was obtained.
Example 42 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(5-carboxymethylthio-1,3,4-thiadiazol-2-yl)-thiomethyl-penem-3-carboxylic acid, disodium salt
A solution of 2-mercapto-5-carboxymethylthio-1,3,4-thiadiazole (41.6 mg, 0.2 mmol) and triethylamine (56 l, 0.4 mmol) in anhydrous tetrahydrofuran was added at -30"C under argon to a solution of tertbutyldiphenylsilyl (5R, 6S)-6-[1 (B) -hydroxyethyl]-2-methanesu lphonyloxy-methyl-penem-3-carboxylate (85 g, 0.15 mmol) in the same solvent. After stirring for 5 hours at -30 C, the reaction mixture was concentrated in vacuo, taken up in ethyl acetate and extracted with water.
The organic layer was discarded, the aqueous layer was made acidic with acetic acid and extracted twice with fresh ethyl acetate. This extract was dried (Na2SO4), concentrated, taken up in THF (3 ml) and stirred for 2 hours with 35% aqueous acetic acid. The reaction mixture was concentrated under high vacuum, treated with a saturated solution of NaHCO3 to a pH of 7.5 and fractionated by a reverse phase column, eluting with water, thus obtaining the title compound (22 mg, 32%).
UV (H2O) A,, 314
NMR (D2O) #ppm 1.25 (3H, d)
3.85 (1H, dd, J=1,5 and 6 Hz)
3.97 (2H, s)
4.2 (1H, m)
4.55 (2H, s)
5.58 (1H, d, J=1.5 Hz).
By proceeding analogously, (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-(5-carboxymethyl 1,3, 4-thiadiazol-2-yl)-thiomethyl-penem-3-carboxylic acid, disodium salt was obtained.
Example 43
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1H-1,2,3-triazol-5-yl)-thiomethyl-penem-3-carboxylate
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-hydroxymethyl -penem-3-carboxylate (80 mg, 0.3 mmol) was sequentially treated with tert-butyldiphenylsilylchloride (78 AI), triethylamine (42 lli), methanesulphonylchloride (24 lli) and finally with 1H-5-mercapto-1,2,3-tdazole sodium salt (43 mg, 0.35 mmol) by following the experimental procedure described in Example 14.
The so-obtained silyl ester-of the title product was directly cleaved with acetic acid-water to afford, after treatment with aqueous NaHCO3 and purification through a LiChroprep RP-18 column, the desired sodium salt (40 mg, 47%).
UV (H2O) A,,,, 314 nm
1R (KBr) γmax 3420, 1770, 1610 cm
MS (FD) m/e (free acid) 328 (M' ). C,1H,2 N4O4S2 requires M, 328.
Example 44
Acetoxymethyl(5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1-(2-dimethylaminoethyl)-1,2,3,4-tetrazol-5-yl]-thiomethylpenem-3-carboxylate
Triethylamine (42 clog, 0.3 mmol) and methanesulphonylchloride (17 l, 0.22 mmol) were sequentially added to a cold (0"C) solution of acetoxymethyl(5R, 6S)-6-[1(R)-hydroxyethyil -2-hydroxymethyl-penem-3carboxylate (60 mg, 0.2 mmol) in a mixture of dichloromethane (4 ml) and tetrahydrofuran (1 ml). When the starting material had disappeared (TLC), the solution was washed with aqueous NaHCO3, then with water, dried and evaporated.The residue was dissolved in ethyl acetate (5 ml), cooled to -30"C and treated with a solution of 5-mercapto -1-(2-dimethylaminoethyll-1,2,3,4-tetrazole hydrochloride (63 mg, 0.3 mmol) and triethylamine (84 l, 0.6 mmol) in tetrahydrofuran (1 ml). The mixture was stirred overnight at -20"C, warmed up to room temperature, washed with water, dried (Na2SO4) and evaporated to give a residue which was purified by reverse phase chromatography (acetonitrile -water mixture as eluant).The title product was thus obtained as a crisp foam (58 mg, 61%) UV (EtOH) A,, 335 nm
IR (nujol) γmax 1785, 1760, 1720 cm
NMR (EtOH-d6) Eppm 1.45 (3H, d, J-- 6.5 Hz)
2.9 (6H, s)
3.65 (3H, t + dd)
4.10 (1H, m)
4.7 (5H, t + ABq)
5.55 (1H, d, J= 1.5 Hz)
5.9 (2H, ABq, J= 6.0 Hz)
Example 45 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-carboxymethyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylic acid disodium salt
By following the experimental procedure described in Example 14, sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-hydroxymethyl-penem-3-carboxylate (100 mg, 0.37 mmol) was sequentially esterified with tertbutyldiphenylsilyl-chloride, mesylated, allowed to react with 1-carboxymethyl-1,2,3,4-tetrazole-5 -thiol (64 mg, 0.4 mmol) in the presence of diisopropylethylamine (0.14 ml, 0.8 mmol), and the silyl ester was eventually hydrolysed by a mixture of THF-H2O-AcOH. Work-up and purification through a reverse phase column afforded the title compound (40 mg, 25%).
UV (H2O) A,,,, 315
NMR (D2O) bppm 1.28 (3H, d, 6.3 Hz)
3.85 (1H, dd, J= 1.4 and 6.3 Hz)
4.2 (1H, m)
4.4 (2H, ABq)
5.3 (2H, s)
5.60 (1H, d, J= 1.4 Hz
Example 46 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1(2-carboxyethyl)-1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-carboxylic acid, disodium salt
When 5-mercapto-l -(2-carboxyethyl)-l ,2,3,4-tetrazole was used in place of 5-mercapto-l -carboxymethyl- 1,2,3,4-tetrazole, the procedure described in the preceeding example gave the title compound.
UV (H2O) #max 315 nm
NMR (D2O) #ppm 1.3 (3H, d)
2.85 (2H, t)
3.9 (1H, dd)
4.2 (1H, m)
4.4 (4H, m)
5.58 (1H, d, J= 1.4 Hz)
MS (FD) m/e (free acid) 401 (M'). C13H15 N > O6S2 requires M, 401.
Example 47 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-(1-pyridinium)-methyl-penem-3-carboxylate, chloride
A solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-chloromethyl-penem-3- carboxylate (58 mg, 0.1 mmol) in dry DMF (0.2 ml) was treated with potassium iodide ( 0.8 mg) and pyridine (0.1 ml). The mixture was stirred for 40 hours at room temperature. Ethyl ether was added with stirring to precipitate a brownish powder which was collected, washed with ether and purified through a reverse phase column (acetonitrile-water as eluants) to give the title product.
UV (EtOH) #max 264,330cm-1 IR(KBr) γmax ' 1795,1750,1710cm-1 Example 48 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(4-carbamoyl-1-pyridinium)methyl-penem-3-carboxylate
A suspension of sodium (5R, 6S)-6-[1(R)-hydroxyethyl] -2-hydroxymethyl-penem-3-carboxylate (100 mg, 0.37 mmol) in dry tetrahydrofuran was stirred with tert-butyldiphenyl-silyl chloride (96 g, 0.37 mmol) for 2 hours at room temperature . The undissolved matter was filtered off and the filtrate was treated at -20 C with trifluoromethanesulphonic anhydride (67 gml, 0.4 mmol) and triethylamine (55 pSl, 0.4 mmol).
After 30 min, a solution of nicotinamide (49 mg, 0.4 mmol) in anhydrous DMF was dropped in, and the resulting mixture was stirred overnight at room temperature. Ethyl acetate (10 ml) and saturated aqueous
NaCI solution (5 ml) were then added. The organic layer was separated, washed again with brine, dried (Na2SO4) and then stirred for 2 hours in dry THF containing 18-Crown-6 (5 mg) and anhydrous KF (10 mg). The mixture was evaporated to a small volume and the residue triturated with ethyl ether. The solid was collected, dissolved in distilled water and purified on a reverse phase column, eluting with water to give the title product.
NMR (D2O) #ppm 1.30 (3H, d, J= 6.5 Hz)
3.90 (1H, dd, J= 1.4 and 6.5 Hz)
4.22 (1H, m)
5.36 -5.66 (2H, ABq)
5.60 (iH, d, J= 1.4 Hz)
8.30-9.08 (4H, m)
Example 49 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-sulphomethyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylic acid, disodium salt.
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-hydroxymethyl-penem-carboxylate (80 mg, 0.3 mmol) in dry
THF was stirred with tert-butyldiphenylsilyl chloride (78 pI) for 2 hours. The insoluble matters were filtered off, the filtrate was cooled to -30"C, treated with NEt3 (42 aI) and methanesulphonyl chloride (25 1) and stirred for a further 10 minutes at -20 C, after which time 1-sulphomethyl-1,2,3,4-tetrazole -5-thiol disodium salt (72 mg, 0.3 mmol) was added portionwise. The mixture was stirred for 6 hours at -20"C, then evaporated in vacuo and triturated with ether.The colleced solid was taken up in a mixture of THF, water and acetic acid (2:2:1), stirred for 2 hours at room temperature evaporated in vacua, taken up with 2% aqueous NaHCO3 solution, washed with ethyl acetate and then passed through a reverse phase column, to give the title product.
UV (H2O) A,,,, 315 IR (KBr) γmax 3400, 1770 and 1610 cm
By proceeding analogously,
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-sulphoethyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylic acid disodium salt was prepared.
By omitting the final treatment with aqueous NaHCO3 the corresponding free acids were obtained:
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-sulphomethyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylic acid
[MS (FD) m/e 423 (M'). C11H13NsO7 S3 requires M,423]; and (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-( l-sulphoethyl-l ,2,3, 4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylic acid.
Example 50 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-(2-sulfoaminoethyl)-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylic acid disodium salt
By following the same procedure described in Example 49, but using S-mercapto-1-(2-sulfoaminoethyll- 1,2,3-4-tetrazole disodium salt instead of 5-mercapto-1-sulphomethyl-1,2,3,4-tetrazole, sodium (5R, 6S)-6 [1(R)-hydroxyethyl]-2-hydroxymethyl-penem-3-carboxylate was converted into the title product in 20% isolated yield.
UV (H20) A,,,, 314 nm
IR (KBr) 'Ymax 3420, 1770 and 1610 cm 1
MS (FD) m/e (free acid) 452 (IM'). C12Hl3 N6O,S3 requires M, 452.
Example 51 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(4-carboxymethyl-5-methyl-1,3-thiazol-2-yl)-thiomethyl-penem-3-carboxylic acid, disodium salt
2-mercapto-4-carboxymethyl-5-methyl-1,3-thiazole disodium salt (58 mg, 0.25 mmol) was added portionwise at -30"C to a stirred solution of tert-butyldiphenylsily1(5R-6S)-6-[1 (R)-hydroxyethyl]-2-methane sulphonyloxymethyl-penem-3 -carboxylate (110 rig, 0.2 mmol) in dry tetrahydrofuran. After 6 hours at -30"C and 3 hours at room temperature the mixture was partitioned between EtOAc and aqueous Na
HCO3. The aqueous layer.was made acidic with ice-cold, 5% citric acid and immediately extracted with fresh ethyl acetate. Hydrolysis of the tert-butyldiphenylsilyl ester was accomplished with 50% aqueous acetic acid (TLC monitoring). The excess HOAc was removed in vacuo and the residue was completely neutralized with aqueous NaHCO3.
Elution with water from a reverse phase column and freeze-drying afforded the title product.
Eleniental analysis found: C, 36.43; H, 3.67; N, 5.52% C16H14N3O6S3Na3.2H3O requires C, 36.28; H, 3.65; N, 5.64%.
Example 52
Sodium (5R, 6S)-[1(R)-hydroxyethyl]-2-(tetrazolo[1,5-b]-pyridazin-6-yl)-thiomethyl-penem-3-carboxylate
By following the experimental procedure described in Example 14, sodium (5R, 6S)-6-[1(R)-hydroxye- methyl]-2-hydroxy-methyl -penem-3-carboxylate (80 mg, 0.3 mmol) was allowed to react with tert-butyldiphenylsilylchloride (78 zI), methanesulphonylchloride (24 ll, triethylamine (42 l) and 6mercaptotetrazolo-[1,5-b]-pyridazine sodium salt 157 mg, 0.35 mmol). Desilylation was finally achieved by stirring a solution of the crude product in THF (2 ml) with 50% aqueous acetic acid (1.5 ml) for 90 min at room temperature.The reaction mixture was concentrated in vacuo, taken up in aqueous NaHCO3 and passed through a reverse phase column, eluting with water, to afford the title product.
IR (KBr) γ max 3430, 1765, 1605 cm
NMR (D2O) #ppm 1.24 (3H, d)
3.82 (1H, dd, J=1.5 and 6.1 Hz)
4.22 (1H, m)
4.66 and 4.96 (each 1H, d, J= 12 Hz)
5.60 (1H, d, J= 1.5 Hz)
7.68 (1H, d, J= 9.6 Hz)
8.38 (1 H, d, J= 9.6 Hz)
Example 53 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(8-carboxytetrazolo-[1,5-b)-pyridazin-6-yl)-thiomethyl-penem-3-carboxylic acid, disodium salt
The title compound was obtained as an amorphous powder (27% yield) when 6-mercapto-8-carboxyte trazolo-[1,5-b]-pyridazine (74 mg, 0.4 mmol) and triethylamine (112 aI, 0.8 mmol) were used in the preceeding example instead of 6-mercaptotetrazolo -[1,5-b]-pyridazine sodium salt.
NMR (D20) #ppm 1.3 (3H, d)
3.9 (1H, dd)
4.2 (1H, m)
4.45 (2H, ABq)
5.6 (1H, d)
8.2 (1H, s)
Example 54
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(8-aminotetrazolo-[1,5-b]-pyridazin-6-yl)-thiomethyl-penem-3-carboxylate
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-hydroxymethyl -penem-3-carboxylate (80 mg, 0.3 mmol) was converted into its tert-butyldiphenylsilyl ester by stirring for 2 hours with tert-butyldiphenylsilylchloride (78 lli, 0.3 mmol) in anhydrous THF. Diphenyl chlorophosphate (62 lli, 0.3 mmol) and triethylamine (42 FI, 0.3 mmol) were added at -20"C to the crude mixture, and the whole was stirred for 15 min in the cold and 30 min at room temperature.The solution was cooled again to -20"C and treated with a solution of 8-amino-6 -mercaptotetrazolo-[1,5-b]-pyridazine (50.5 mg, 0.3 mmol) and triethylamine (83 l, 0.6 mmoll in THF (3 ml). After overnight stirring at -20"C, the reaction mixture was concentrated in vacuo and partitioned between EtOAc and aqueous NaHCO3. The organic layer, containing the tert-butyl-diphenyisilyl ester of the title product, was dried over Na2SO4, freed from the solvent and the residue was directly taken up ina mixture of THF, AcOH, and H2O (1:1:1, 5ml).After completion of the silyl ester hydrolysis (TLC monitoring), the crude mixture was concentrated in vacuo, made neutral with enough aqueous NaHCO3 and then purified by reverse phase column chromatography, thus obtaining the title product as a foam.
IR (KBr) γ max 1760, 1660, 1625 cm
NMR (D2O) 8 ppm 1.3013H, d) 3.77 (1H, dd, J= 1.8 and 6.5 Hz) 4.18 (1H,m)
4.55 (2H,br s)
5.50 (1H, d, J= 1.8Hz) 6.50 (1H,s) Example 55 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(2-methyl-5-oxo-6-hydroxy-2,5-dihydro-1,2,4-triazin-3-yl)-thiomethyl-penem-3-carboxylic acid, disodium salt
A solution of p-nitrobenzyl(5R, GS)-6-[1(R)-p-nitrobenzyl -oxycarbonyloxyethyl]-2-methanesulphonyloxymethyl-penem -3-carboxylate (63 mg, 0.1 mmol) in dry THF (3 ml), cooled to - 30 C, was treated with a solution of 2-methyl-3-mercapto -5-oxo-6-hydroxy-2,5-dihydro-1,2,4-triazine (24 mg, 0.15 mmol) and triethylamine (42 yl, 0.3 mmol) in the same solvent.
After 30 min at -30"C, the mixture was allowed to reach room temperature, and then concentrated in vacuo. The residue was taken up with ethyl acetate, washed with water, dried (Na2SO4) and evaporated.
After purification by reverse phase chromatography, the so-obtained di-p-nitrobenzyl intermediate, dissolved in THF (1ml), was vigorously stirred with 1 M aqueous solution of NH4CI (5 ml) and iron powder (0.3 g).
Upon completion of the reaction (TLC monitoring), the mixture was treated with aqueous NaHCO3, filtered, the filtrate washed with ethyl acetate, concentrated to a syrup which was purified through a Li
Chroprep. RP-18 column (water as eluant), thus affording the title product.
NMR (D2O) #ppm 1.25(3H, d)
(200MHz apparatus) 3.65 (3H, s)
3.82 (1H, dd, J= 1.6 and 5.9 Hz)
4.20 (1H, m)
4.59 (2H, ABq, J=14.5 Hz, separation of inner lines 14.9 Hz)
5.55 (iH, d, J= 1.6 Hz)
By omitting the treatment with NaHCO3, and purifying directly the hydrolysis mixture, the corresponding (5R, 6S) -6-[1 ( R )-hyd roxyethyl ]-2-(2-methyl-5-oxo-6-hyd roxy-2, 5-oxo-6-hydroxy-2,5-dihyd ro-1,2,4-tria zin-3-yl)-thiomethyl -penem-3-carboxylic acid was obtained.
Similarly, the free acid of the compounds described in the examples 13, 38, 41, 44, 45, 46, 51, 52, 54 and 65 were prepared, namely:
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-(-[(1-methyl-1,2,3,4-tetrazol-5-yl)-thiomethyl]-penem-3-carboxylic acld ;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1-(2-cyanoethyl)-1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-carboxylic acid;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1-(2-cyanomethyl)-1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-carboxylic acid;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-(5-carboxymethylthio-1,3,4-(thiadiazol-2-yl)-thiomethyl-penem-3-carboxylic acid;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-(5-carboxymethyl-1,3,4-thiadiazol-2-yl)-thiomethyl-penem-3-carboxylic acid;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-carboxymethyl-1,2,3,4-tetrazol-5-yl)-thiomethyl-penem-3-carboxylic acid;; (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-[1 (2-carboxyethyl)-1 ,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-carboxylic acid;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-(4-carboxymethyl-b-methyl-1,3-thiazol-2-yl)-thiomethyl-penem-3-carboxylic acid; (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-(tetrazolo[l ,5-b] pyridazin-6-yl)-thiomethyl-penem-3-carboxylic acid; (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-(8-carboxytetrazolo [1 ,5-blpyridazin-5-yl)-thiomethyl-penem-3-carboxylic acid; (5R, 6S)-6-[1 (R)-hyd roxyethyl]-2-(8-a minotetrazolo [1,5-b] pyridazin-6-yl)-thiomethyl-penem-3-carboxylic acid; (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-[l-(2-sulfoaminoethy -1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-carbox- ylic acid; ; (5R, 6S)-6-[1 (R)-hydroxyethyl[-2-[1-(2-aminocarbonylethyl) -1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-car- boxylic acid;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1-(2-aminocarbonylmethyl)-1,2,3,4-tetrazo[-5-yl]-thiomethyl-penem-3carboxylic acid;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-[2-(2-dimethylaminoethyl)-1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3-carboxylic acid;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-[1-(2-dimethylaminomethyl)-1,2,3,4-tetrazol-5-yl]-thiomethyl-penem-3carboxylic acid; (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(6-methoxy-pyrazin-2 -yl)-thiomethyl-penem-3-carboxylic acid;
(5R, 6S)-6-[1(R)-hydroxyethyl]-2-(2-amino-1,3,4-thiadiazol-5-yl)-thiomethyl-penem-3-carboxylic acid ; and (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-(1,2,3,4-tetrazol-5-yl-thiomethyl-penem-3-carboxylic acid.
Example 56 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-(4-methyl-5-oxo-6-hydroxy-4,5-dihydro
1,2,4-triazin-3-yl)-thiomethyl-penem-3-carboxylate
A solution of p-nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-hydroxymethyl-penem-3- carboxylate (100 mg, 0.18 mmol) in dry dichloromethane (10 ml) was sequentially treated at -25"C with triethylamine (28 pI, 0.18 mmol). The mixture was allowed to warm up to room temperature, then washed with diluted NaHCO3 solution, dried (Na2SO4) and evaporated.
The residue was dissolved in dry THF (5 ml), treated with a second amount of triethylamine (28 S followed by 3-mercapto -4-methyl-5-oxo-6-hydroxy-4,5-dihydro-1,2,4-triazine (32 mg, 0.2 mmol). After 3 hours stirring at 0"C, the solvent was evaporated in vacuo and the residue chromatographed (silica gel, ethyl acetate as eluants) to afford the title product as a white solid.
IR (CHCI3 liquid film) y max 1785, 1750, 1710, 1685 cm
NMR (CDCI3) 3 ppm 1.46 (3H, d, J= 7 Hz)
3.42 (3H, s)
3.97 (1H, dd, J= 1.8 and 7.0 Hz)
4.47 (2H, ABq, J= 15 Hz, separation of inner lines 7 Hz)
5.07 -5.47 (5H, m)
5.60 (1H, d, J= 1.7 Hz) 7.49 (2H, d, J= 8.5 Hz)
7.60 (2H, d, J= 8.5 Hz)
8.16 (4H, d, J= 8.5 Hz)
Hydrolysis of the protecting groups as described in Example 55 lead to (5R, 6S)-6-[1(R)-hydroxyethyl]-2- (4-methyl-5-oxo -6-hydroxy-4,5-dihydro-1 ,2,4-triazin-3-yl)-thiomethyl-penem -3-carboxylic acid.
Example 57 p-Nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxyethyl]-2-(2-aminothiozol-5-yl)-thiomethyl-penem-3-carboxylate
Starting from p-nitrobenzyl(5R, 6S)-6-[1(R)-p-nitrobenzyloxycarbonyloxythyl]-2-methanesulphonyloxy- methyl-penem -3-carboxylate (63 mg, 0.5 mmol), the experimental procedure described in example 56 led to the title compound (28 mg, 42%)
UV (EtOH) A,,, 325 nm IR (nujol) γ γmax 3200-3400, 1785, 1755, 1710 MS (FD) mle 673 (M ). C27H23N5Olo S3 requires M, 673
Hydrolysis of the obtained compound according to the procedure of the Example 55 led to (5R, 6S)-6 1(R)-hydroxy-ethyl] -2-(2-aminothiazol-5-yll-thiomethyl-penem-3-carboxylic acid.
Example 58
Allyl (5R, 6S)-6-[1(R)-tert-butyldimethylsilyloxyethyl]-2-methanesulphonyloxymethylpenem-3-carboxylate
A solution of allyl (5R, 6S)-6-[1(R)-tert-butyldimethylsiltloxyethyl]-2-hydroxymethyl penem-3-carboxylate (200 mg) in dry, ethanol-free dichloromethane (10 ml) was treated at -40"C under nitrogen with triethylamine (77 l) and then with mesyl chloride (41 pull. The temperature was let rise to 20"C, the mixture was washed with water, dried over Na2SO,, and the solvent evaporated to give an oil which is conveniently used as such for displacement reactions with sulphur nucleophiles as reported, e.g., in the following examples,
A sample purified by short-path chromatography showed the following spectral properties::
UV (CHCl3) A max 328 nm (F = 6,249)
1R (film) γ ,, 1793, 1710, 1590, 1360 and 1175 cm
Example 59
Allyl (5R, 6S)-6-p[1(R)-tert=butyldimethylsilyloxyethyl]-2-(4-methyl-5-oxo-6-hydroxy-4,5-dihydro-1,2,4-triazin3-yl)-thiomethyl-penem-3-carboxylate
A cold solution of 6-hydroxy-3-mercapto-4-methyl-4,5-dihydro -1,2,4-triazin-5-one (100 mg) and triethylamine (0.157 ml) in tetrahydrofuran (20 ml) was added to a solution of allyl (5R, 6S) -6-[1(R)-tert-butyldi- methylsilyloxyethyl]-2-metanesulphonyl -oxymethyl-penem-3-carboxylate (240 mg) in the same solvent, and the mixture was kept overnight at approximately 0"C, The solvent was evaporated and the residue partitioned between EtOAc and water. Removal of the solvent from the dried organic extracts, followed by silica gel chromatography (ethyl acetate -cyclohexane) afforded the title product as a white, amorphous solid,
UV (CHC13) A ,, 280 (F = 9,103) and 321 nm (e = 8,738)
IR (CHCl3) y max 3210, 1790, 1710 and 1590 cm- NMR (CDCl3) #ppm 0.06 (6H,s),
0.89 (9H, s)
1.22 (3H, d),
3.14-3.53 (2H, m),
3.46 (3H, s),
3.72 (1H, dd, J=2 and 4Hz),
4.28 (1H, m),
4.50 (2H, center of ABq),
4.72 (2H, m),
5.58 (1H, d, J=2Hz), and
11.0 (1H, broad s)
Example 60
Allyl (5R, 6S)-6-(1(R)-hydroxyethyl]-2-(4-methyl-5-oxo-6-hydroxy-4,5-dihydro-1,2,4-triazin-3-yl)-thiomethyl penem-3-carboxylate
A solution of ally (5R, 6S)-6-[1(R)-tert-butyldimethylsilyloxyethyl]-2-(4-methyl-5-oxo-6-hydroxy-4,5-dihy- dro -1,2,4-triazin-3-yl)-thiomethyl-penem-3-carboxylate (130 mg) in tetrahydrofuran (3 ml) was treated with acetic acid (0.14 ml) and tetrabutylammonium fluoride trihydrate (228 mg). After 18 h at room temperature, the mixture was evaporated to dryness under vacuum and fractioned through a silica gel column (merck 60 HR 230-400 Mesh B=1.5 cm, h=12 cm).Elution with neat ethyl acetate and then with
EtOAc EtOH 9:1 afforded the title product;
UV (EtOH) A,, 251 (E=7,840) and 318 nm (F=7,770) IR (CHCl3 film) γ γmax 3400 br, 1785, 1710 br cm NMR (CDCl3) #ppm 1.34 (3H, d),
3.44 (3H, s),
3.78 (1H, dd, J=2 and 6.5 Hz),
4.22 (1H, m),
4.47 (2H, broad s),
4.72 (2H, m),
5.25 and 5.40 (each IH, broad d),
5.62 (IH, d, J=2Hz),
5.96 (IH, m), and 11(1 H, broads).
Example 61 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(4-methyl-5-oxo-6-hydroxy-4,5-dihydro-1,2,4-triazin-3-yl)thiomethyl-penem-3-carboxylic acid sodium salt
Triphenylphosphine (10 mg) and tetrakis (triphenylphosphine) palladium (0) (10 mg) were added to a solution of allyl (5R, 6S) -6-[1(R)-hydroxyethyl]-2-(4-methyl-5-oxo-6-hydroxy-4, 5-dihydro-1,2,4-triazin-3- yl)thiomethyl-penem-3-carboxylate (60 mg) in a 2:1 mixture of tetrahydrofuran and dichloromethane (1.5 ml). After 30 min stirring, a 0.5 M solution of sodium ethylhexanoate in 1:1 tetrahydrofuran/dichloromethane (0.3 ml) was added.
The mixture was stirred for a few minutes and let stand for 1 hour at -30 C. The precipitated solid was isolated by repeated centrifugations and washings with fresh dichloromethane, then dried under vacuum to afford 56 mg of the title product;
UV (H2O) A,,,, 304 nm (F=8,330) IR [KBr) γ γmax 3420, 2960, 2920, 1760, 1700, 1610 and 1580 cm Example 62
Allyl (5R, 6S)-6-[1(R)-tert-butyldimethylsilyloxyethyl]-2-(2-methyl-5-oxo-6-tert-butyldiphenylsilyloxy-2,5-dihydro- 1,2,4triazin-3-ylJ-thiomethyl-penem-3-carboxylate
A solution of 2-methyl-3-mercapto-6-hydroxy-2,5-dihydro -1,2-4-triazin-5-one (0.8 g) in dry tetrahydrofuran (25 ml) was stirrred for 30 minutes with treithylamine (0.835 ml) and tertbutyldiphenylsilylchloride (1.53 ml). The reaction mixture was partitioned between 1% aqueous NaHCO3 and ethyl acetate. Removal of the solvent from the dried organic layer left a residue which crystallized by trituration with light petrol affording 2-methyl-3-mercapto-6-tert-butyldiphenylsilyloxy -2,5-dihydro-1,2,4-triazin-5-one (1.34 g), m.p.
135'C (decomp): UV (CHClj) #max 278 (F=20,820) and 320 sh ( =4,460) nm
IR (CHCI3) w,,,,, 1720, 1580 cm
NMR (CDCl3) #ppm 1.1 (9H, s),
3.4 (3H, s)
7.2-7.7 (10 H, m)
9.9 (1H, br s)
B) A solution of triphenylphosphine (472 mg) in dry distilled THF (12 ml) was treated at 0 C with ethyl azodicarboxylate (282 ml, dissolved in 2 ml of the same solvent). After 1 hour-stirring at 0"C, this solution was added under stirring to a solution of the product obtained under A) (630 mg) and of allyl (5R, 6S) -6 [1 (R)-tert-butyldimethylsilyloxyethyl]-2-hydroxymethyl-penem-3-carboxylate (600 mg) in dry distilled THF (6 ml).
Soon at the end of the addition the reaction was over (tlc monitoring, SiO2, EtOAc/C,H12 1:2); the solvent was removed and the crude material was freed from some polar contaminants by flash chromatography (SiO2, ethyl acetate -cyclohexane), thus obtaining 1 g of the title product;
UV (CHCl3) $max 333 nm ;
IR (CHCl3 film) γ; 1787, 1705, 1665 cm 1 NMR (CDCI3) #ppm (inter alia) 3.30 (3H, s),
3.66 (1H, dd),
4.20 (1H, m),
4.65 (4H, m),
5.15 -5.50 (2H, m),
5.54 (1H, d),
5.70-6.15 (1H, m)
Example 63
Allyl (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(2-methyl-5-oxo-6-hydroxy-2,5-dihydro-1,2,4-triazin-3-yl)thiomethyl penem-3 -carboxylate
The bis-silylated material obtained in Example 62 (Ig), dissolved in dry tetrahydrofuran (16 ml) was stirred for 22 hours at room temperature in the presence of acetic acid (0.76 ml) and tetrabutylammonium fluoride trihydrate (1.26 g).The solvent was removed in vacuo, the residue taken up in a small amount of water (#10 ml) and passed through a reverse-phase column (Merck LiChroprep RP-18 0 2 cm, h=10 cm), eluting first with water, then with H2O/EtOH 4:1 and finally with H2O/EtOH 2:1.The title product was obtained from the last fractions by removal of the ethanol followed by freeze-drying (350 mg);
IR (CHCl3 film) γmax 3400 br, 1750, 1700 br cm l Example 64 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(2-methyl-5-oxo-6-hydroxy-2,5-dihydro-1,2,4-triazin-3-yl)thiomethyl-penem-3-carboxylic acid, disodium salt
A solution of allyl (5R, 6S)-6-[1 (B)-hydroxyethyl]-2-(2 -methyl-5-oxo-6-hydroxy-2,5-dihydro-1,2, 4-triazin 3-yl) thiomethyl-penem-3-carboxylate (300 mg) in a mixture of tetrahydrofuran (5 ml) and dichloromethane (2 ml) was treated under stirring with triphenylphosphine (30 mg) and tetrakis (triphenylphosphine) palladium (O) (30 mg), soon followed by a 0.5 M solution of sodium ethylhexanoate in 1::1 THF/CH2CI2 (2.86 ml). The white precipitate was collected by centrifugation, triturated in CH2CI2 and centrifugated again (twice), then dissolved in a small amount of water and passed through a reverse-phase column (Merck LiChroprep RP-18) eluting with distilled water. The product-containing fractions (Merck Kieselgel 60 F 254 silanisiert, CHCI3/CH3OH/HCOOH 90:15::10, Rf=0.3) were collected and evaporated to afford the title product;
UV A,,,, 277 and 308 (sh) nm;
IR (KBr) γmax 3420, 2960, 2920, 1760, 1640 and 1605 cm
NMR (D2O) (200 MHz apparatus) #ppm 1.25 (3H, d),
3.65 (3H, s),
3.82 (1H, dd), J=1.6 and 5.9 Hz),
4.20 (1H, m),
4.59 (2H, ABq, J=14.5 Hz, separation of inner lines 14.9 Hz),
5.55 (1H, d, J=1.6 Hz)
Example 65
By starting from the appropriate precursors, and following the experimental procedure described in
Example 58-61 (method A in the following table) or the one described in Examples 62-64 (method B in the table), the herebelow tabulated compouds were obtained;;
-1 Code number R Method ax(HqOJ } NMR (Ds0),Sppm N-H max(KBr) 2o,ppm ICE 31;jl ' N/ FCE 2Z,;Z l 1) il; ~ same data report CH,C07Na ed in example 45.
FCE '2,;; J N A ji4 3600-3200, same data report 2960,2920, ed ln example 46 CH2CH2CO2Wa 27o,1763, - 13So,13o 2) FCE 22S-o tt A ;1; 1r66,1630 1.29fjH.d),2.93 broad (6H.a).3.73(2..t), - - ,CH j.filH.dd,J-2 2CH2NHo and 4.5Hz) 4.ZS (lH,m)..5712fl.ABq) 4,9012H,t),j.ó4 oN (lH,d,J=2Hzl FCE 22734 + ?lob A 312 3430,30to, 1.2,1t3H,d),3.E2 3040,2960, (lH,dd,J-l.; and 7920,23;0, 6.1Hz!,4.22tlH.m}, 175,16OS, 4.66 and 4.96(each 1370 1H.d.3"12}iz).5.60 ilH.d,J=1.5Hz ! . 7.68 and 8.38 leach 1H.
d,J-9.6 Hzl
NH2 NH FCE 2:846 3 X A 299 3500-310, 1.30i3H,dl,3.j; I;bo,iaoJ; (IH,dd,J=1.3 and 1625,1570 6.5Hz),4.15(1H, e) ,1.55(2H,br s', ;.;O(IH,d.J=l.SHz N 6.50( s) FCE 22364; 0 0 A A 326 6.j0(1H,s) 1o35tiH di.i 7 CH3 2960,20.20, )1)),dd),3.o7)3H, 2200,1765, s).A.3))H,m),4.60 1620,1;,0, )ZH,ABq),5.5511H, l;;O,1520, d)".ê3-e.0j 2H.m) 1190 .xHi 5441;2; 5)cH3 A A ;4iO,2960, 1.37tjH,dl,2.77 3 2920,2a60, (3H,s',3.i,(1H,dd) 176;,1;70 4-iO(IH.m),4.6~ (2H,A11qI,5.62I 1H, d) FCE 22923J T ) - NH A ~ 3420,3300. I.jSljH,dl,j.PZilH 5 2 3150,2960, dd),).25i1H.ml, 2920,2zoo. 4.41(2H,s),5.o4 1765,1510 (IH.d) AM 11,;6;! 4 ss B 314 1,6;.l60S - k FCE ZlgSaji 1 FCE 22983; 47 1sN B 315 3400,1770, - 1695,1610 CII,, CH,, CONH N - N FCE 223623 4 ' A 316 3430,2960, 1.26í3H.d'.3.23 N 2920,2iso, 12H.tF,3.34(1H, 2250,1765, dd,J.1.A and cHC1,CN 1615 6Hz) ,1.20) H,,, 4.S4(2H,ABq,J,14.2 Hz,sep.of winner lines 12Hz),4. (2H,t),S.5,8 lH,d. . I .1Hz
1) During the synthesis, the carboxy group on the heterocyclic thiol was protected as its ally ester.
2, Isolated as the internal salt with the 3-penemcarboxylate anion.
3) Isolated as the potassium salt, by using potassium ethylhexanoate.
Example 66
Following analogous procedure as the one described in examples 58 to 61, the herebelow listed compounds were synthesized: (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-methylimidazol-2-yl) -thiomethyl-penem-3-carboxylic acid, isolated as the sodium salt;
UV (H2O) A,, 315 nm;
NMR (200 MHz, D2O) Gppm 1.21(3H,d, J=6.4 Hz),
3.72 (3H, s)
3.76 (1H, dd, J=1.4 and 6 Hz),
4.13 (2H, ABq, J=14 Hz, separation of inner lines 36 Hz),
4.14 (1H, ml, 5.51 (1H, d, J= 1.4 Hz),
7.04 and 7.21 (each 1H, d, J=1.3 Hz), (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-[1 -(1,2,3,4-tetrazol -5-yl-methyl)-l ,2,3,4-tetrazol-5-yl]-thiomethyllpenem-3 -carboxylic acid, isolated as the sodium salt;
UV (H2O) A,,, 256 and 314 nm.
By replacing sodium ethylhexanoate with a molar excess of acetic acid, the aforementioned compounds were isolated as the free acids. Moreover, the following ones were also prepared: (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-(3-amino-l ,2, 4-triazol-5-yl)-thiomethyl-penem-3-carboxylic acid;
UV (H2O) A,,,, 262 and 310 nm; and (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-(1 ,2,3-thiadiazol-5-yl) -thiomethyl-penem-3-carboxylic acid;
UV (H2O) #max 330 nm;
MS (FD) m/e 345 (M+) C11H12N3O4S3 requires M 345.
Example 67
Allyl (5R, 6S)-6-[1(R)-tert-butyl-dimethylsilyloxyethyl]-2-(1,2,4-triazol-5-yl) thiomethyl-penem-3-carboxylate
A solution of 4(R)-(1 ,2,4-triazol-5-yl)-thioacetylthio-3 (S)-1(R)-tert-butyl-dimethylsilyloxyethyl -1-[1-allyloxy -carbonyl)-1 -triphenylphosphoranylidenemethyll-azetidin-2-one (0.45 g) in toluene (50 ml) was refluxed under nitrogen atmosphere for three hours.
Short column chromatography on silica gel with dichloromethane; ethylacetate (8:2) as eluant gave 0.25 g of pure title compound;
NMR (CDCI,), eippm - 0.06 (6H, s), 0.89 (9H,s), 1.35 (3H, d, J=7 H,) 3.88(1H,dd, J=2 and 5 H,), 4.25 (1H,m), 4.6(4H, m), 5.1-5.4(2H, m), S.5011H,d, J-2H,), 5.6-6.1 (1H, m), 8.17(1H. br s).
Example 68
Allyl (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1,2,4-triazol-5-yl)-thiomethyl-penem-3-carboxylate
A solution of the compound obtained in example 67 (0.380 g) in tetrahydrofuran (8 ml) was treated with acetic acid (0.5 ml) and tetrabutylammonium fluoride trihydrate (0.69 g) until the starting material had disappeared (TLC monitoring) (14-24 hrs).The reaction mixture was evaporated in vacuo and then chromatographed (SlO2 column, ethyl acetate-cyclo-hexane mixtures) thus obtaining the title compound;
IR (CHCl3 film) 3380 br, 1785, 1715 cm
Example 69 (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1,2,4-triazol-5-yl)-thiomethylpenem-3-carboxylic acid, sodium salt
A solution of the allyl ester obtained in example 68 (0.2 g) in tetrahydrofuran (1 ml) was sequentially treated with triphenylphosphine (0.7 g) and tetrakis (triphenyl-phosphine) palladium (O) (0.07 g), followed after a few minutes by a 0.5 M solution of sodium ethylhexanoate in 1:1 THF/dichloromethane (2.1 ml).
After 15 minutes stirring, ethyl was added to precipitate the title compound as a yellowish powder, which was collected by filtration. washed several times with dichloromethane and vacuum-dried;
UV (H2O) Amax 314 nm; IR (KBr) ymax 1765 and 1620 br cm 1
Operating in analogous way and starting from the appropriate intermediates obtained according to the procedure described in the examples 67 and 68, also the compounds mentioned in the examples 38, 42, 44, 48, 49, 56, 57, 65 and 66 were prepared.
Example 70
Acetoxymethyl (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1-methyl-1,2,3,4-tetrazol-5-yl)thiomethylpenem-3-carboxylate
A) A solution of sodium (5R, 6S)-6-[1 (R)-hydroxyethyl] 2 -(1-methyl-1,2,3,4-tetrazol-S- yl)thiomethylpenem-3-carboxylate (3.1 g) in dry dimethylformamide (25 ml) was kept overnight in the presence of bromomethyl acetate (2.2 g). After further 2 hours at room temperature, the reaction mixture was partitioned between brine and ethyl acetate.After several washings with brine, the organic phase was dried and evaporated to a residue which was triturated with ethyl ether light petrol, thus obtaining the title compound as a white powder;
IR (KBr) 1795, 1760, 1720cm
NMR (acetone d-6), 8ppm (inter alia):
1.25 (3H, d), 2.06 (3H, s), 3.75 (1H, dd), 5.83 (2H, ABq), 5.69 (1H, d, J=1.5Hz)
B) A solution of acetoxymethyl (5R, 6S)-6-L1 (R)-tert -butyldimethylsilyloxyethyl]-2-(l -methyl-1 ,2,3,4-tetra- zol -5-yl)thiomethylpenem-3-carboxylat (1 g) obtained as described in Example 30] in dry THF, was stirred for 20 hours at room temperature in the presence of acetic acid (1 ml) and tetrabutylammonium fluoride (1.5 g).Removal of the solvent and partition between ethyl acetate and water, followed by evaporation, furnished the title compound.
Example 71
Following analogous procedure to the one described under A) in Example 70, or the one described in
Example 30 and Example 70 under B), the herebelow listed compounds were obtained;
acetoxymethyl (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(1,2,3-thiadiazol-5-yl) thiomethylpenem-3-carboxylate ;
acetoxymethyl (5R, 6S)-6-[1 (R)-hydroxyethyl]-2-(2-methyl -5-oxo-6-hydroxy-2,5-dihydro-l ,2,4-triazin-3-yl) thiomethyl-penem-3-carboxylate; and
acetoxymethyl (5R, GS)-6-[1(R)-hydroxyethyl]-2-(tetrazolo [1,5-b] pyridazin-6-yl)thiomethylpenem-3-car- boxylate.
Example 72
Allyl (5R, 6S)-6-[1(R)-tert-butyldimethylsilyloxyethyl]-2-(2-p-nitrobenzyloxycarbonylaminoethyl)-thiomethylpenem-3-carboxylate
Triphenylphosphine (131 mg, 0.5 mmol) and diethylazodicarboxylate (78 lli, 0.5 mmol) in 1.8 ml of dry distilled tetrahydrofuran were allowed to react for 30 minutes at 0 C. To this mixture, allyl (5R, 6S)-6 [1(R)-tert-butyldimethyl -silyloxyethyl]-2-hydroxymethylpenem-3-carboxylate (100 mg, 0.35 mmol) in THF (5 ml), soon followed by cysteamine p-nitrobenzylcarbonate (100 mg, 0.4 mmol). were added. The mixture was let rise to room temperature while stirring. After 30 minutes, the solvent was removed in vacuo and the residue was chromatographed (silica gel, ethyl acetate-cyclohexane) to afford the title product as a yellowish syrup.
IR (film) γmax 1790, 1750, 1710 cm
NMR (CDCI3) #ppm 0.06 (6H, s), 0.94 (9H, s), 1.32 (3H, d), 2.56 (2H, t, J= 7Hz), 3.40 (2H, t of doublets,
J= 7Hz), 3.85 (IH, dd, J= 2 and 6.5 Hz), 4.0-4.3 (3H, m), 4.65 (2H, m), 5.1 -5.4 (2H, m), 5.25 (2H, s), 5.60 (1H, d, J= 2 Hz), 5.70 -6.15 (1H, m), 7.60 and 8.30 (each 2H, d, J Hzi ppm.
Example 73
Sodium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(2-aminoethyl) -thiomethylpenem-3-carboxylate
A solution of allyl (5R, 6S)-6-[1(R)tert-butyidimethylsilyloxyethyl]-2-(2-p- nitrobenzyloxycarbonylaminoethyll thio-methylpenem-3-carboxylate (150 mg, 0.23 mmol) in THF (2 ml) ws stirred for 24 hours with acetic acid (100 lli) and tetrabutylammonium fluoride (165 mg). Removal of the solvent and short-path chromatography yielded allyl (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(2-p-nitrobenzy- loxycarbonylamino ethyl) thiomethyl-penem-3-carboxylate in almost quantitative yield.This material was dissolved in a mixture of THF (1 ml) and dichloromethane (1 ml), then triphenylphosphine (8 mg) and tetrakis-triphenyl-phosphine-Pd(O) (8 mg), were added under argon, soon followed by sodium ethylhexanoate (36 mg). After 5 min stirring, the mixture was diluted with ethyl ether and filtered, thus collecting sodium (5R, 6S)-6-[1 (R)-hydroxy -ethyl]-2-(2-p-nitrobenzyloxycarbonyla minoethyl )thiomethyl -penem-3carboxylate (70 mg) as a white powder. This compound was directly dissolved in a mixture of THF (5 ml) and of pH 7.0 phosphate buffer (5 ml) and shaked in a hydrogen atmosphere with 10% Palladium on charcoal (two portions, 50 mg each, added at 15 min interval).The catalyst was filtered off, the liquors were washed with ethyl acetate and the aqueous phase was concentrated in vacuo and then chromatographed on a reverse-phase column, eluting with water. The product-containing fractions (UV, Amax 314 nm) were collected and freeze-dried, thus obtaining 20 mg of the title product:
IR (KBr) ymax 1770, 1610 cm
UV (H2O) .max 314 nm.
Example 74
Reaction of allyl (5R, 6S)-6-[1(R)-tert-butyldimethylsilyloxyethyl]-2-hydroxymethylpenem-3-carboxylate with the appropriate heterocyclic thiol and the preformed complex between triphenylphosphine and diethylazodicarboxylate, followed by sequential cleavage of the silyloxy and allyloxy protecting groups, according to the general methodologies illustrated in the foregoing examples, afforded:
Potassium (5R, 6S)-6-[1(R)-hydroxyethyl]-2-(pyrazin-2-yl)-thiomethylpenem-3-carboxylate ; UV (H2O) #m 250 (F = 10,344) and 319 (F = 8,682) nm; IR (KBr) ymax 3400, 1760, 1600 cm 1;NMR (D2O) 3ppm 1.26 (3H, d, J- 6.5 Hz), 3.07 (1H, dd, J= 1 and 4 Hz), 4.2 (1H, m), 4.54 (2H, s), 5.47 (1H, d, J= 1Hz), 8.32-8.06 (3H, m, Ar);
Potassium (5R, 6S)-6-[1(R)hydroxyethyl]-2-(4-ethyl-1,3, 4-triazol-3-yl)-thiomethylpenem-3-carboxylate; UV (H2O) Amax 316 nm (F = 5,600); IR (KBr) ymax 3420, 1765, 1600 cm 1;
NMR (D2O) Appm 1.26 (3H, d, J= 6.6 Hz), 1.42 (3H, t, J= 5.6 Hz), 3.77 (1H, dd, J= 1.6 and 8.1 Hz), 4.17 (2H, q, J- 5.6 Hz), 4.2 (1H, m), 4.2 and 4.43 (2H, each d, J= 14 Hz), 5.52 (1H, d, J= 1.6 Hz), 8.55 (1H, s); (5R, 6S)-6-[1 (Rl-hydroxyethyl]-2-(S-carboxymethylthio -1 ,3,4-thiadiazol-2-yl)thiomethyl penem-3-carboxylic acid, dipotassium salt; IR (KBr) ymax 3380, 1755, 1610 cm l; NMR (D2O) #ppm 1.25 (3H, d), 3.85 (1H, dd, 1.5 and 6 Hz), 3.97 (2H, s), 4.2 (1H, m), 4.55 (2H, s), 5.57 (1H, d, j= 1.5 Hz)
Claims (13)
1. A process for the preparation of a compound of the following formula (I)
wherein
R1 is hydrogen or an organic group;
R2 is hydrogen or a carboxy protecting group; and Y is
a) a group -S-Het wherein Het is an optionally substituted saturated or unsaturated heterocyclic ring containing at least one heteroatom chosen from 0, S and N;
b) a C1-Cl2 alkylthio group optionally substituted by one or more substituents chosen from halogen, formyl C2 -C, acyl, amino, hydroxy and mercapto, wherein the amino, hydroxy and mercapto groups may optionally be in a protected form; or
c) an optionally substituted pyridyl group; and the pharmaceutically orveterinarily acceptable salts thereof, said process comprising reacting a compound of formula (II).
wherein R1 and R2 are as defined above and L is chlorine, bromine or a free or activated hydroxy group, with a compound of formula (Ill) Y-H (Ill wherein Y is as defined above, or a salt thereof, or a reactive derivative thereof and, if desired, converting an obtained compound of formula (í) into another compound of formula (I) and/or, if desired, salifying a free compound of formula (I) or, if desired, obtaining a free compound of formula (I) from a salt thereof and/or, if desired, separating a mixture of isomers of formula (I) into the single isomers.
2. A process according to claim 1 wherein the activated hydroxy group L in the compound of formula (II) is a hydroxy group activated in the form of a reactive ester or reactive complex or reactive acetal.
3. A process according to claim 2 wherein the reactive ester is an ester with a sulphonic or a phosphoric or a carboxylic acid.
4. A process according to claim 2 wherein the reactive complex is a complex comprising a derivative or trivalent phosphorus and a C1-C, alkyl ester of the azodicarboxylic acid.
5. A process according to claim 2 wherein the reactive acetal is the mixed acetal between the compound of formula (II) wherein L is hydroxy and neopentyl alcohol, and dimethylformamide.
6. A process according to any one of the preceding claims wherein the reactive derivative of the compound of formula (III) is one of a compound of formula (III) wherein Y is a group -S-Het, and is the complex between the disulfide thereof -S-Het, and is the complex between the disulfide thereof Het-S-S-Het and an.aryl or C,-C6 alkyl derivative of trivalent phosphorus,
7. A process according to claim 1 for the preparation of a compound of formula (I), comprising reacting a compound of formula (II) wherein L is chlorine or bromine or a hydroxy group activated in the form of a reactive ester with a sulphonic or a phosphoric acid, with a compound of formula (III) as such or as a salt.
8. A process according to claim 1 for the preparation of a compound of formula (I) wherien Y is a group -S-Het or a C,-C12 alkylthio group as defined in claim 1, comprising reacting a compound of formula (It) wherein L is a hydroxy group activated in the form of a reactive ester with a carboxylic acid, or in the form of a reactive complex or in the form of a reactive acetal, with a compound of formula (III) wherein Y is -S-Het or C1-C12 alkylthio, as such or as a salt.
9. A process according to claim 1 for the preparation of a compound of formula (I) wherein Y is a group -S-Het, comprising reacting a compound of formula (Ill wherein L is a free hydroxy group with a reactive derivative of compound of formula (III) wherein Y is -S-Het.
10. A process according to any one of claims 1 to 9 for the preparation of a compound of the formula (Ia)
wherein
R'. is a C,-C, alkyl group substituted by a free or protected hydroxy;
R2 is a hydrogen or a carboxy protecting group; and Y' is
1) an optionally substituted pyridyl group; or
2) a group -S-alk-NH2 wherein alk is C1-C3 alkylene; or
3) a group -S-Het' wherein Het' represents
(a) 1,3,4-thiadiazolyl either unsubstituted or substituted by a substituent chosen from
(a') C2-Calkyl; (b') C,-C, alkyl substituted by an optionally salified carboxy group; (c') an optionally salified carboxymethylthio group; and
(d') a group -N -w. wherein each of R' and R" is independently, hydrogen or Cl-C3 alkyl;
b) 1,2,3-thiadiazolyl optionally substituted by a C1 -C, alkyl group;
c) 1,2,3-triazolyl substituted by a Cl-C6 alkyl group;
d) 1,2,4-triazolyl optionally substituted by a group -N =R- wherein R' and R" are as defined above;
e) 1,3,4-triazolyl optionally substituted by a Cl-C6 alkyl group;
f) imidazolyl optionally substituted by a Cl-C6 alkyl group;
g) thiazolyl optionally substituted by one or more substituents chosen from (a') -N fl. wherein R' and R" are as defined above; (b') unsubsituted Cl-C6 alkyl; and (c') Cl-C3 alkyl substituted by an optionally salified carboxyl group; h) tetrazolyi optionally substituted by (a') unsibstituted C1-C6 alkyl, or (b') C1-C3 alkyl substituted by a substituent chosen from (i) optionally salified carboxy, (ii) optionally salified sulpho or sulfoamino, (iii) cyano, (iv) carbamoyl, (v) -N wherein R' and R" are as defined above, and (vil tetrazolyl; i) pyrazinyl substituted by C1-C, alkyl or C1-C, alkoxy group;
I) 5-oxo-6-hydroxy-2,5-dihydro-1,2,4-triazinyl and 5-oxo -6-hydroxy-4,5-dihydro-1,2,4-triazinyl, both optionally substituted by a C1-C3 alkyl group; or
m) tetrazolo-pyridazinyl optionally substituted by (a') an optionally salified carboxy group or (b') a group -N # wherein R' and R" are as defined above; provided that when Y' is a group -S-Het' wherein Het' is 1,2,3,4-tetrazol-5-yl substituted by C1-C6 alkyl at the 1-position, then R'1 is not hydroxyisopropyl, and the pharmaceutically or veterinarily acceptable salts thereof.
11. A compound having the formula (II) reported above in claim 1 wherein R1 is an organic group and
L is a hydroxy group activated in the form of a reactive ester with a sulphonic acid.
12. A process according to claim 1 substantially as hereinbefore described with references to any one of Examples 12 to 14, 16, 18, 20 to 23, 25, 26, 28 to 30, 33, 36 to 57, 59 to 66 and 68 to 74.
13. A process according to claim 10 substantially as hereinbefore described with reference to any one of the Examples 12 to 14, 16, 18, 20 to 23, 25, 26, 28 to 30, 33, 36 to 38, 40 to 57, 59 to 66 and 68 to 74.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB08520253A GB2162185B (en) | 1982-04-08 | 1985-08-13 | New process for preparation of substituted penem derivatives |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8210410 | 1982-04-08 | ||
GB08520253A GB2162185B (en) | 1982-04-08 | 1985-08-13 | New process for preparation of substituted penem derivatives |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8520253D0 GB8520253D0 (en) | 1985-09-18 |
GB2162185A true GB2162185A (en) | 1986-01-29 |
GB2162185B GB2162185B (en) | 1986-07-30 |
Family
ID=26282515
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08520253A Expired GB2162185B (en) | 1982-04-08 | 1985-08-13 | New process for preparation of substituted penem derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2162185B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0331395A1 (en) * | 1988-03-01 | 1989-09-06 | Taiho Pharmaceutical Company Limited | Process for preparing 2-alpha-methyl-2-beta-(1,2,3-triazol-1-yl)methyl-penam-3-alpha-carboxylic acid derivatives |
-
1985
- 1985-08-13 GB GB08520253A patent/GB2162185B/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0331395A1 (en) * | 1988-03-01 | 1989-09-06 | Taiho Pharmaceutical Company Limited | Process for preparing 2-alpha-methyl-2-beta-(1,2,3-triazol-1-yl)methyl-penam-3-alpha-carboxylic acid derivatives |
Also Published As
Publication number | Publication date |
---|---|
GB8520253D0 (en) | 1985-09-18 |
GB2162185B (en) | 1986-07-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19950407 |