CA1096373A - Ureido substituted cephalosporin antibiotics - Google Patents
Ureido substituted cephalosporin antibioticsInfo
- Publication number
- CA1096373A CA1096373A CA223,530A CA223530A CA1096373A CA 1096373 A CA1096373 A CA 1096373A CA 223530 A CA223530 A CA 223530A CA 1096373 A CA1096373 A CA 1096373A
- Authority
- CA
- Canada
- Prior art keywords
- alpha
- methyl
- cephem
- ylthiomethyl
- carboxylic acid
- 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.)
- Expired
Links
- 229940124587 cephalosporin Drugs 0.000 title claims abstract description 36
- 229930186147 Cephalosporin Natural products 0.000 title claims abstract description 35
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 title claims abstract description 13
- 239000003242 anti bacterial agent Substances 0.000 title abstract description 20
- 229940088710 antibiotic agent Drugs 0.000 title abstract description 20
- 150000001780 cephalosporins Chemical class 0.000 title description 26
- -1 cephalosporin compounds Chemical class 0.000 claims abstract description 52
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 47
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 46
- 150000001875 compounds Chemical class 0.000 claims description 46
- 238000000034 method Methods 0.000 claims description 31
- 239000001257 hydrogen Substances 0.000 claims description 30
- 229910052739 hydrogen Inorganic materials 0.000 claims description 30
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 18
- 150000002431 hydrogen Chemical class 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 14
- 125000005059 halophenyl group Chemical group 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- IKBDQDKEPPQHAA-UHFFFAOYSA-N (4-nitrophenyl) n-(methylcarbamoyl)carbamate Chemical compound CNC(=O)NC(=O)OC1=CC=C([N+]([O-])=O)C=C1 IKBDQDKEPPQHAA-UHFFFAOYSA-N 0.000 claims description 8
- NXJZQSRAFBHNLI-UHFFFAOYSA-N 2-oxoimidazolidine-1-carbonyl chloride Chemical compound ClC(=O)N1CCNC1=O NXJZQSRAFBHNLI-UHFFFAOYSA-N 0.000 claims description 8
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims description 8
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims description 8
- JIQBLONORFFMKH-UHFFFAOYSA-N n-methyl-n-(methylcarbamoyl)carbamoyl chloride Chemical compound CNC(=O)N(C)C(Cl)=O JIQBLONORFFMKH-UHFFFAOYSA-N 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 231100000252 nontoxic Toxicity 0.000 claims description 7
- 230000003000 nontoxic effect Effects 0.000 claims description 7
- 125000005042 acyloxymethyl group Chemical group 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- 125000005633 phthalidyl group Chemical group 0.000 claims description 6
- AIILPZZSUTZJIO-UHFFFAOYSA-N (4-nitrophenyl) n-(phenylcarbamoyl)carbamate Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC(=O)NC(=O)NC1=CC=CC=C1 AIILPZZSUTZJIO-UHFFFAOYSA-N 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 5
- 125000001544 thienyl group Chemical group 0.000 claims description 5
- RYQPJEPACDMMMB-UHFFFAOYSA-N (4-nitrophenyl) n-carbamoylcarbamate Chemical compound NC(=O)NC(=O)OC1=CC=C([N+]([O-])=O)C=C1 RYQPJEPACDMMMB-UHFFFAOYSA-N 0.000 claims description 4
- ZWTPALHHEULAPI-UHFFFAOYSA-N 3-methylsulfonyl-2-oxoimidazolidine-1-carbonyl chloride Chemical compound CS(=O)(=O)N1CCN(C(Cl)=O)C1=O ZWTPALHHEULAPI-UHFFFAOYSA-N 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 4
- 125000002541 furyl group Chemical group 0.000 claims description 4
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 21
- 239000000126 substance Substances 0.000 claims 21
- 241000965481 Darksidea alpha Species 0.000 claims 12
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 4
- 244000005700 microbiome Species 0.000 abstract description 9
- 208000015181 infectious disease Diseases 0.000 abstract description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 78
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 66
- 239000000047 product Substances 0.000 description 44
- 239000011541 reaction mixture Substances 0.000 description 31
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 29
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 28
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 27
- 239000000243 solution Substances 0.000 description 27
- 238000002360 preparation method Methods 0.000 description 25
- 239000000203 mixture Substances 0.000 description 24
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- 238000005917 acylation reaction Methods 0.000 description 18
- SIOVKLKJSOKLIF-UHFFFAOYSA-N bis(trimethylsilyl)acetamide Chemical compound C[Si](C)(C)OC(C)=N[Si](C)(C)C SIOVKLKJSOKLIF-UHFFFAOYSA-N 0.000 description 18
- 239000000725 suspension Substances 0.000 description 18
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 17
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 16
- 230000010933 acylation Effects 0.000 description 16
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 15
- 238000003756 stirring Methods 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 238000005481 NMR spectroscopy Methods 0.000 description 12
- 230000000694 effects Effects 0.000 description 12
- 239000010410 layer Substances 0.000 description 12
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 11
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 10
- QHFKWIKCUHNXAU-UHFFFAOYSA-N (4-nitrophenyl) carbamate Chemical compound NC(=O)OC1=CC=C([N+]([O-])=O)C=C1 QHFKWIKCUHNXAU-UHFFFAOYSA-N 0.000 description 9
- 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 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000000706 filtrate Substances 0.000 description 9
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 8
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 8
- 239000008346 aqueous phase Substances 0.000 description 8
- 229910052786 argon Inorganic materials 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 229960005419 nitrogen Drugs 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 7
- 235000013877 carbamide Nutrition 0.000 description 7
- 239000012456 homogeneous solution Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- NXLNNXIXOYSCMB-UHFFFAOYSA-N (4-nitrophenyl) carbonochloridate Chemical compound [O-][N+](=O)C1=CC=C(OC(Cl)=O)C=C1 NXLNNXIXOYSCMB-UHFFFAOYSA-N 0.000 description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 6
- 230000003115 biocidal effect Effects 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000000921 elemental analysis Methods 0.000 description 6
- 239000012442 inert solvent Substances 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- RMKZBDOVNUBHRJ-UHFFFAOYSA-N (4-nitrophenyl) n-carbamoyl-n-methylcarbamate Chemical compound NC(=O)N(C)C(=O)OC1=CC=C([N+]([O-])=O)C=C1 RMKZBDOVNUBHRJ-UHFFFAOYSA-N 0.000 description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 239000004202 carbamide Substances 0.000 description 5
- 239000000284 extract Substances 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 229930192474 thiophene Natural products 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 238000000862 absorption spectrum Methods 0.000 description 4
- 125000001309 chloro group Chemical group Cl* 0.000 description 4
- PEHSSTUGJUBZBI-UHFFFAOYSA-N indan-5-ol Chemical compound OC1=CC=C2CCCC2=C1 PEHSSTUGJUBZBI-UHFFFAOYSA-N 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 238000010626 work up procedure Methods 0.000 description 4
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 3
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 3
- 239000012267 brine Substances 0.000 description 3
- 125000001246 bromo group Chemical group Br* 0.000 description 3
- FUBBGQLTSCSAON-PBFPGSCMSA-N cefaloglycin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)COC(=O)C)C(O)=O)=CC=CC=C1 FUBBGQLTSCSAON-PBFPGSCMSA-N 0.000 description 3
- 229950004030 cefaloglycin Drugs 0.000 description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 3
- MHYCRLGKOZWVEF-UHFFFAOYSA-N ethyl acetate;hydrate Chemical compound O.CCOC(C)=O MHYCRLGKOZWVEF-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- FYFWFZGKGINKQA-UHFFFAOYSA-N (4-nitrophenyl) n-(benzylcarbamoyl)carbamate Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC(=O)NC(=O)NCC1=CC=CC=C1 FYFWFZGKGINKQA-UHFFFAOYSA-N 0.000 description 2
- LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 2
- 229930182555 Penicillin Natural products 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 241000194017 Streptococcus Species 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 239000000370 acceptor Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- NHYXMAKLBXBVEO-UHFFFAOYSA-N bromomethyl acetate Chemical compound CC(=O)OCBr NHYXMAKLBXBVEO-UHFFFAOYSA-N 0.000 description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
- 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 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000012433 hydrogen halide Substances 0.000 description 2
- 229910000039 hydrogen halide Inorganic materials 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 description 2
- GPULBFUXMLBYEI-UHFFFAOYSA-N n-(carbamoylamino)carbamoyl chloride Chemical compound NC(=O)NNC(Cl)=O GPULBFUXMLBYEI-UHFFFAOYSA-N 0.000 description 2
- GRRYSIXDUIAUGY-UHFFFAOYSA-N n-methylcarbamoyl chloride Chemical compound CNC(Cl)=O GRRYSIXDUIAUGY-UHFFFAOYSA-N 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- IOUDFJIYHNEOJB-UHFFFAOYSA-N (4-nitrophenyl) n-(ethylcarbamoyl)carbamate Chemical compound CCNC(=O)NC(=O)OC1=CC=C([N+]([O-])=O)C=C1 IOUDFJIYHNEOJB-UHFFFAOYSA-N 0.000 description 1
- JLMTUDOXHAJDHH-UHFFFAOYSA-N (4-nitrophenyl) n-(furan-2-ylmethylcarbamoyl)carbamate Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC(=O)NC(=O)NCC1=CC=CO1 JLMTUDOXHAJDHH-UHFFFAOYSA-N 0.000 description 1
- NOYVLDUFCHRHTP-UHFFFAOYSA-N (4-nitrophenyl) n-(prop-2-ynylcarbamoyl)carbamate Chemical compound [O-][N+](=O)C1=CC=C(OC(=O)NC(=O)NCC#C)C=C1 NOYVLDUFCHRHTP-UHFFFAOYSA-N 0.000 description 1
- WAMKIBHTCHTCFY-UHFFFAOYSA-N (4-nitrophenyl)methyl n-(methylcarbamoyl)carbamate Chemical compound CNC(=O)NC(=O)OCC1=CC=C([N+]([O-])=O)C=C1 WAMKIBHTCHTCFY-UHFFFAOYSA-N 0.000 description 1
- IKWLIQXIPRUIDU-ZCFIWIBFSA-N (6r)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Chemical compound OC(=O)C1=CCS[C@@H]2CC(=O)N12 IKWLIQXIPRUIDU-ZCFIWIBFSA-N 0.000 description 1
- DKYBVKMIZODYKL-UHFFFAOYSA-N 1,3-diazinane Chemical compound C1CNCNC1 DKYBVKMIZODYKL-UHFFFAOYSA-N 0.000 description 1
- ADFXKUOMJKEIND-UHFFFAOYSA-N 1,3-dicyclohexylurea Chemical compound C1CCCCC1NC(=O)NC1CCCCC1 ADFXKUOMJKEIND-UHFFFAOYSA-N 0.000 description 1
- 229940057054 1,3-dimethylurea Drugs 0.000 description 1
- ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical compound C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 description 1
- DUJAUTCYDLIGAY-UHFFFAOYSA-N 2-(furan-2-ylamino)acetic acid Chemical compound OC(=O)CNC1=CC=CO1 DUJAUTCYDLIGAY-UHFFFAOYSA-N 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- YOETUEMZNOLGDB-UHFFFAOYSA-N 2-methylpropyl carbonochloridate Chemical compound CC(C)COC(Cl)=O YOETUEMZNOLGDB-UHFFFAOYSA-N 0.000 description 1
- MDQHTWMXYBVSHU-UHFFFAOYSA-N 2-trimethylsilylacetamide Chemical compound C[Si](C)(C)CC(N)=O MDQHTWMXYBVSHU-UHFFFAOYSA-N 0.000 description 1
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 1
- YSRBHIYWSUGRIF-UHFFFAOYSA-N 3-acetyl-2-oxo-1,3-diazinane-1-carbonyl chloride Chemical compound CC(=O)N1CCCN(C(Cl)=O)C1=O YSRBHIYWSUGRIF-UHFFFAOYSA-N 0.000 description 1
- CLMSHAWYULIVFQ-UHFFFAOYSA-N 3-bromo-3h-2-benzofuran-1-one Chemical compound C1=CC=C2C(Br)OC(=O)C2=C1 CLMSHAWYULIVFQ-UHFFFAOYSA-N 0.000 description 1
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 description 1
- 125000004208 3-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(*)=C1[H] 0.000 description 1
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 description 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- HSHGZXNAXBPPDL-HZGVNTEJSA-N 7beta-aminocephalosporanic acid Chemical compound S1CC(COC(=O)C)=C(C([O-])=O)N2C(=O)[C@@H]([NH3+])[C@@H]12 HSHGZXNAXBPPDL-HZGVNTEJSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- 241000147019 Enterobacter sp. Species 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 206010061126 Escherichia infection Diseases 0.000 description 1
- 241000588748 Klebsiella Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 1
- MGJKQDOBUOMPEZ-UHFFFAOYSA-N N,N'-dimethylurea Chemical compound CNC(=O)NC MGJKQDOBUOMPEZ-UHFFFAOYSA-N 0.000 description 1
- JRJZERFYNJJDDX-UHFFFAOYSA-N N-(2-amino-2-oxoethyl)-N-methylcarbamoyl chloride Chemical compound CN(C(=O)Cl)CC(=O)N JRJZERFYNJJDDX-UHFFFAOYSA-N 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000334216 Proteus sp. Species 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 1
- 241000607720 Serratia Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 241001221452 Staphylococcus faecalis Species 0.000 description 1
- 241000193996 Streptococcus pyogenes Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- PNNCWTXUWKENPE-UHFFFAOYSA-N [N].NC(N)=O Chemical compound [N].NC(N)=O PNNCWTXUWKENPE-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 238000002814 agar dilution Methods 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- YXASHNSJWVCWQQ-UHFFFAOYSA-N bromomethyl propanoate Chemical compound CCC(=O)OCBr YXASHNSJWVCWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- GGRHYQCXXYLUTL-UHFFFAOYSA-N chloromethyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OCCl GGRHYQCXXYLUTL-UHFFFAOYSA-N 0.000 description 1
- SMJYMSAPPGLBAR-UHFFFAOYSA-N chloromethyl acetate Chemical compound CC(=O)OCCl SMJYMSAPPGLBAR-UHFFFAOYSA-N 0.000 description 1
- BOXZXICVMMSYPE-UHFFFAOYSA-N chloromethyl benzoate Chemical compound ClCOC(=O)C1=CC=CC=C1 BOXZXICVMMSYPE-UHFFFAOYSA-N 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 1
- 229910000071 diazene Inorganic materials 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229940043237 diethanolamine Drugs 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 208000020612 escherichia coli infection Diseases 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 229940031098 ethanolamine Drugs 0.000 description 1
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000011065 in-situ storage 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
- 239000011261 inert gas Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- 238000004452 microanalysis Methods 0.000 description 1
- 244000000010 microbial pathogen Species 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- BSCHIACBONPEOB-UHFFFAOYSA-N oxolane;hydrate Chemical compound O.C1CCOC1 BSCHIACBONPEOB-UHFFFAOYSA-N 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 150000002960 penicillins Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 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
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 239000005051 trimethylchlorosilane Substances 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D501/14—Compounds having a nitrogen atom directly attached in position 7
- C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
- C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
- C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
- C07D501/36—Methylene radicals, substituted by sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C273/18—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
- C07C273/1854—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas by reactions not involving the formation of the N-C(O)-N- moiety
- C07C273/1863—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas by reactions not involving the formation of the N-C(O)-N- moiety from urea
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C273/00—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C273/18—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
- C07C273/1854—Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas by reactions not involving the formation of the N-C(O)-N- moiety
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
The present invention relates to novel ureido substituted cephalosporin compounds which are highly active broad spectrum antibiotics especially useful in the treatment of infections attributable to the gram-negative microorganisms.
The present invention relates to novel ureido substituted cephalosporin compounds which are highly active broad spectrum antibiotics especially useful in the treatment of infections attributable to the gram-negative microorganisms.
Description
1t~9~:;373 The present invention relates to novel ureido substituted cephalosporin compounds which are highly active broad spectrum antibiotics especially useful in the treatment of infections attributable to the gram-negative microorganisms.
Cephalosporin compounds having a ureido or a substituted ureido substituent in the ~-position of the 7-acylamido side chain have been described. In U.S. Patent 3,673,183 issued June 27, 1972, a-ureidocephalosporanic acids are disclosed. Acyloxymethyl esters of a-ureidocyclo-hexadienylacetamidocephalosporins are described in U.S.
Patent 3,708,479 and of a-aminobenzylpenicillin in U.S.
Patent 3,697,507. Penicillins and cephalosporins having an ~-(3-imidoylureido)arylacetamido side chain are described in U.S. Patents 3,634,405 and 3,646,024, respectively. a-3-Acylureidobenzylpenicillins also are known wherein a wide variety of acyl groups are attached to the terminal nitrogen of the a-ureido group of the 6-arylacetamido side chain.
The compounds provided by this invention differ structurally from the compounds of the prior art in that the cephalosporin dihydrothiazine ring is substituted in the 3-position with a heterocyclicthiomethyl group. In addition, the cephalosporin antibiotics described herein can be characterized as expanded spectrum cephalosporin antibiotics in that they not only possess the usual high level of activity against gram-positive microorganisms but they also possess a high level of activity against a broad spectrum of gram-negative microorganisms which the prior art compounds did not possess.
~L~96373 This invention relates to new ureido substituted cephalosporin antibiotic compounds represented by the following general formula I -O H O H
R--C--N--C~C-N--t--~ ~
Rl o~ CH2--R2 I
wherein R is a 3-substituted ureido group represented by the ormula H O .
l 11 R' '--N--C--N--R ' wherein R'' is hydrogen, Cl-C3 alkyl, allyl, propargyl, C3-C6 cycloalkyl, phenyl, benzyl, or furfuryl; R' is hydrogen or methyl;
or R is a cyclic ureido group of the formula O
Y- N~ ~N .
(CH2)n wherein Y is hydrogen, acetyl or methanesulfonyl, and _ is 2 or 3;
l~ i . --3 ~09~i37~
R1 is phenyl, hydroxyphenyl, halophenyl, hydroxy substituted halophenyl, ~ or R2 is acetoxy, -S-~ ~ \5 ~ or -S- ~ N N
Z Z
wherein Z is Cl-C lower alkyl;
R3 is hydrogen, indanyl, phthalidyl, an acyloxymethyl group of the formula o -CHz{~_y~
wherein Y' is C1-C4 alkyl or phenyl, and when R3 is hydrogen, the pharmaceutically acceptable non-toxic salts thereof.
~ -4-~gt~73 In the foregoing definition, the cyclic ureido groups represented are the five-membered imidazolidine-2-one-1-yl group (n = 2) and the six-membered hexahydropyrimidine-2-one-1-yl group represented by the formulae R
y ~ ~ and Y ~ ~
\~/
wherein Y is H-, CH3S02- or (CH3)2C(O)-.
The term "halogen" as used herein refers to fluoro, chloro, and bromo and preferably chloro.
Representative of the substituted phenyl groups, (Rl) hydroxyphenyl, halophenyl, and hydroxy substituted ~'~ ```
~L~9G37~
halophenyl are 4-chlorophenyl, 4-bromophenyl, 3-fluoro-phenyl, 4-hydroxyphenyl, 3-hydroxyphenyl, 3-chloro-4-hydroxyphenyl, 2-chlorophenyl, 3,4-dichlorophenyl, 3,5-dichlorophenyl, 3,5-dihydroxyphenyl, 2-hydroxyphenyl, 4-hydroxy-3,5-dichlorophenyl, and 4-hydroxy-3,5-dibromophenyl.
The term "Cl-C4 lower alkyl", represented by Z in the above formula, refers to methyl, ethyl n-propyl, iso-propyl, n-butyl, t-butyl, and like straight and branched chain Cl-C4 hydrocarbon radicals.
The term C3-C6 cycloalkyl refers to cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
The cephalosporin antibiotic compounds represented by the formula I, when R3 is hydrogen, are prepared by acylating a 7-(D-a-amino-a-arylacetamido)-3-cephem-4-carboxylic acid represented by the formula II, O H
H2N-CH-C-N-I - t ~ 'I
Rl o~ ~ ~ -CH2-R2 II
COOH
wherein Rl and R2 have the previously defined meaningsJ
1~963''~3 O H
R1 o~t ~ ~ ~-CH2-R2 II
COOH
wherein Rl and R2 are as defined above, with a compound of the formula O
R-C-A
wherein R is as defined above and A is -Cl or {)~ NO2 ~ /
and if desired converting the acid so obtained wherein R3 is hydrogen to the corresponding ester wherein R3 is other than hydrogen ~
and where desired, when R is hydrogen, forming a pharmaceutically acceptable, non-toxic salt of said compound of formula I.
The compounds of formula I wherein R is the 1,3-disubstituted ureido group -6a-1~963~;'3 H~O
l ll R''-N-C-N- (Formula I, R'=CH3) and R" is other than hydrogen are prepared by acylating the cephalosporin compound II with the corresponding carbamoyl chloride, .
H O O
R''-N-C-N-C-CI
- The compounds of the formula I wherein R is a cyclic ureido group are prepared by the acylation of II with a cyclic ureido carbamoyl chloride of the formula Il O
Y~
~ CHa)n wherein Y is hydrogen, acetyl or methanesulfonyl, and n is 2 or 3.
The compounds of the formula I wherein R is a 3-substituted ureido group ~L~i9G,~73 ~1 0 .
R''-N-C-N- (Formula I, R'=H~
H
are prepared by the acylation of II with a p-nitrophenyl carbamate H O H O
R''-N-C-N-C-O--~ ~ --NOz =--The starting materials represented by the formula II wherein Rl is a phenyl, substituted phenyl, or thienyl group and R2 is a l-lower alkyl-lH-tetrazole-5-yl group or a 5-lower alkyl-1,3,4-thiadiazole-2-yl group are described by Ryan in U.S. Patent 3,641,021. Compounds of the formula II
wherein Rl is a furyl group are prepared by the acylation of a 7-amino nucleus compound of the formula H~N-~
t COOH
with the anhydride formed with a-(t-butyloxycarbamido)-furanacetic acid and isobutylchloroformate. Following the ~9~i~73 acylation the t-butyloxycarbonyl protecting group is removed by known methods, for example, with trifluoroacetic acid in the cold, or alternatively with p-toluenesulfonic acid in acetonitrile as described by Chauvette in U.S. Patent 3,769,281.
The starting materials represented by formula II
wherein R2 is the acetoxy group are prepared by the acylation of 7-aminocephalosporanic acid with a phenyl, thienyl, or furyl glycine. The compound of the formula II wherein Rl is phenyl and R2 is acetoxy is the well known antibiotic, cephaloglycin.
The acylation of a compound of the formula II with the 1,3-disubstituted-ureidocarbamoyl chloride H O O
l 11 11 R ' ' -N-C-N-C-C I
or the cyclic ureidocarbamoyl chloride involves the acylation of the free a-amino group in the 7-position side chain. The acylation is carried out in an inert solvent in the presence of a hydrogen halide acceptor at a temperature between about -5C. and 20C. and preferably at about 0-5C. Sol-vents such as acetonitrile, tetrahydrofuran, dimethylform-amide and dimethylacetamide can be used in the acylation. A
preferred solvent is acetonitrile. Should the starting material be insoluble or partly insoluble in the solvent, it can be solubilized by the addition of a silylating agent such as bis-(trimethylsilyl~acetamide tBsA) before the ~96373 ; the addition of the carbamoyl chloride.
Hydrogen halide acceptors which can be used include the tertiary amines such as triethylamine and pyridine and the alkylene oxides such as propylene oxide or butylene oxide.
The carbamoyl chlorides R''-N-C-N-C-CI
are prepared by reacting the 1,3-disubstituted urea with phosgene in a dry, inert solvent such as dichloroethane, dichloromethane or tetrahydrofuran. The reaction is prefer-ably carried out in the cold at about 0-5C.
The symmetrical 1,3-dimethylurea affords but one carbamoyl chloride, namely, N-methylaminocarbonyl-N-methylcarbamoyl chloride CH3-N-C-N-C-CI (R"=methyl) since both nitrogen atoms of the urea are equivalent.
The unsymmetrical ureas, wherein R" is a group other than methyl, can form two carbamoyl chlorides on reaction with phosgene. The desired N-methylcarbamoyl chloride R''-N-C-N - C-CI
is separated from the undesired isomeric chloride by frac-tional crystallization from mixtures of polar and non-polar 1~9~3~
organic solvents such as mixtures of diethyl ether and petroleum ether, and acetone or ethyl acetate mixed with hexane or petroleum ether.
The 1,3-disubstituted ureas are prepared by well known methods or are commercially available.
Illustrative N-substituted-aminocarbonyl-N-methyl-carbamoyl chlorides are represented by the foregoing formula wherein R" is ethyl, H2C=CH-CH2-(allyl), HC-C-CH2-(propargyl), phenyl, benzyl, 2-furfuryl, cyclopropyl and cyclohexyl.
The cyclic ureido carbamoyl chlorides Il o Y-N ~~C-CI
(CH~)n wherein Y and n are as defined above are prepared by react-ing the substituted (Y=acetyl or methylsulfonyl) or unsubsti-tuted (Y=H), imidazolidine-2-one(n=2) or hexahydropyrimidine-
Cephalosporin compounds having a ureido or a substituted ureido substituent in the ~-position of the 7-acylamido side chain have been described. In U.S. Patent 3,673,183 issued June 27, 1972, a-ureidocephalosporanic acids are disclosed. Acyloxymethyl esters of a-ureidocyclo-hexadienylacetamidocephalosporins are described in U.S.
Patent 3,708,479 and of a-aminobenzylpenicillin in U.S.
Patent 3,697,507. Penicillins and cephalosporins having an ~-(3-imidoylureido)arylacetamido side chain are described in U.S. Patents 3,634,405 and 3,646,024, respectively. a-3-Acylureidobenzylpenicillins also are known wherein a wide variety of acyl groups are attached to the terminal nitrogen of the a-ureido group of the 6-arylacetamido side chain.
The compounds provided by this invention differ structurally from the compounds of the prior art in that the cephalosporin dihydrothiazine ring is substituted in the 3-position with a heterocyclicthiomethyl group. In addition, the cephalosporin antibiotics described herein can be characterized as expanded spectrum cephalosporin antibiotics in that they not only possess the usual high level of activity against gram-positive microorganisms but they also possess a high level of activity against a broad spectrum of gram-negative microorganisms which the prior art compounds did not possess.
~L~96373 This invention relates to new ureido substituted cephalosporin antibiotic compounds represented by the following general formula I -O H O H
R--C--N--C~C-N--t--~ ~
Rl o~ CH2--R2 I
wherein R is a 3-substituted ureido group represented by the ormula H O .
l 11 R' '--N--C--N--R ' wherein R'' is hydrogen, Cl-C3 alkyl, allyl, propargyl, C3-C6 cycloalkyl, phenyl, benzyl, or furfuryl; R' is hydrogen or methyl;
or R is a cyclic ureido group of the formula O
Y- N~ ~N .
(CH2)n wherein Y is hydrogen, acetyl or methanesulfonyl, and _ is 2 or 3;
l~ i . --3 ~09~i37~
R1 is phenyl, hydroxyphenyl, halophenyl, hydroxy substituted halophenyl, ~ or R2 is acetoxy, -S-~ ~ \5 ~ or -S- ~ N N
Z Z
wherein Z is Cl-C lower alkyl;
R3 is hydrogen, indanyl, phthalidyl, an acyloxymethyl group of the formula o -CHz{~_y~
wherein Y' is C1-C4 alkyl or phenyl, and when R3 is hydrogen, the pharmaceutically acceptable non-toxic salts thereof.
~ -4-~gt~73 In the foregoing definition, the cyclic ureido groups represented are the five-membered imidazolidine-2-one-1-yl group (n = 2) and the six-membered hexahydropyrimidine-2-one-1-yl group represented by the formulae R
y ~ ~ and Y ~ ~
\~/
wherein Y is H-, CH3S02- or (CH3)2C(O)-.
The term "halogen" as used herein refers to fluoro, chloro, and bromo and preferably chloro.
Representative of the substituted phenyl groups, (Rl) hydroxyphenyl, halophenyl, and hydroxy substituted ~'~ ```
~L~9G37~
halophenyl are 4-chlorophenyl, 4-bromophenyl, 3-fluoro-phenyl, 4-hydroxyphenyl, 3-hydroxyphenyl, 3-chloro-4-hydroxyphenyl, 2-chlorophenyl, 3,4-dichlorophenyl, 3,5-dichlorophenyl, 3,5-dihydroxyphenyl, 2-hydroxyphenyl, 4-hydroxy-3,5-dichlorophenyl, and 4-hydroxy-3,5-dibromophenyl.
The term "Cl-C4 lower alkyl", represented by Z in the above formula, refers to methyl, ethyl n-propyl, iso-propyl, n-butyl, t-butyl, and like straight and branched chain Cl-C4 hydrocarbon radicals.
The term C3-C6 cycloalkyl refers to cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
The cephalosporin antibiotic compounds represented by the formula I, when R3 is hydrogen, are prepared by acylating a 7-(D-a-amino-a-arylacetamido)-3-cephem-4-carboxylic acid represented by the formula II, O H
H2N-CH-C-N-I - t ~ 'I
Rl o~ ~ ~ -CH2-R2 II
COOH
wherein Rl and R2 have the previously defined meaningsJ
1~963''~3 O H
R1 o~t ~ ~ ~-CH2-R2 II
COOH
wherein Rl and R2 are as defined above, with a compound of the formula O
R-C-A
wherein R is as defined above and A is -Cl or {)~ NO2 ~ /
and if desired converting the acid so obtained wherein R3 is hydrogen to the corresponding ester wherein R3 is other than hydrogen ~
and where desired, when R is hydrogen, forming a pharmaceutically acceptable, non-toxic salt of said compound of formula I.
The compounds of formula I wherein R is the 1,3-disubstituted ureido group -6a-1~963~;'3 H~O
l ll R''-N-C-N- (Formula I, R'=CH3) and R" is other than hydrogen are prepared by acylating the cephalosporin compound II with the corresponding carbamoyl chloride, .
H O O
R''-N-C-N-C-CI
- The compounds of the formula I wherein R is a cyclic ureido group are prepared by the acylation of II with a cyclic ureido carbamoyl chloride of the formula Il O
Y~
~ CHa)n wherein Y is hydrogen, acetyl or methanesulfonyl, and n is 2 or 3.
The compounds of the formula I wherein R is a 3-substituted ureido group ~L~i9G,~73 ~1 0 .
R''-N-C-N- (Formula I, R'=H~
H
are prepared by the acylation of II with a p-nitrophenyl carbamate H O H O
R''-N-C-N-C-O--~ ~ --NOz =--The starting materials represented by the formula II wherein Rl is a phenyl, substituted phenyl, or thienyl group and R2 is a l-lower alkyl-lH-tetrazole-5-yl group or a 5-lower alkyl-1,3,4-thiadiazole-2-yl group are described by Ryan in U.S. Patent 3,641,021. Compounds of the formula II
wherein Rl is a furyl group are prepared by the acylation of a 7-amino nucleus compound of the formula H~N-~
t COOH
with the anhydride formed with a-(t-butyloxycarbamido)-furanacetic acid and isobutylchloroformate. Following the ~9~i~73 acylation the t-butyloxycarbonyl protecting group is removed by known methods, for example, with trifluoroacetic acid in the cold, or alternatively with p-toluenesulfonic acid in acetonitrile as described by Chauvette in U.S. Patent 3,769,281.
The starting materials represented by formula II
wherein R2 is the acetoxy group are prepared by the acylation of 7-aminocephalosporanic acid with a phenyl, thienyl, or furyl glycine. The compound of the formula II wherein Rl is phenyl and R2 is acetoxy is the well known antibiotic, cephaloglycin.
The acylation of a compound of the formula II with the 1,3-disubstituted-ureidocarbamoyl chloride H O O
l 11 11 R ' ' -N-C-N-C-C I
or the cyclic ureidocarbamoyl chloride involves the acylation of the free a-amino group in the 7-position side chain. The acylation is carried out in an inert solvent in the presence of a hydrogen halide acceptor at a temperature between about -5C. and 20C. and preferably at about 0-5C. Sol-vents such as acetonitrile, tetrahydrofuran, dimethylform-amide and dimethylacetamide can be used in the acylation. A
preferred solvent is acetonitrile. Should the starting material be insoluble or partly insoluble in the solvent, it can be solubilized by the addition of a silylating agent such as bis-(trimethylsilyl~acetamide tBsA) before the ~96373 ; the addition of the carbamoyl chloride.
Hydrogen halide acceptors which can be used include the tertiary amines such as triethylamine and pyridine and the alkylene oxides such as propylene oxide or butylene oxide.
The carbamoyl chlorides R''-N-C-N-C-CI
are prepared by reacting the 1,3-disubstituted urea with phosgene in a dry, inert solvent such as dichloroethane, dichloromethane or tetrahydrofuran. The reaction is prefer-ably carried out in the cold at about 0-5C.
The symmetrical 1,3-dimethylurea affords but one carbamoyl chloride, namely, N-methylaminocarbonyl-N-methylcarbamoyl chloride CH3-N-C-N-C-CI (R"=methyl) since both nitrogen atoms of the urea are equivalent.
The unsymmetrical ureas, wherein R" is a group other than methyl, can form two carbamoyl chlorides on reaction with phosgene. The desired N-methylcarbamoyl chloride R''-N-C-N - C-CI
is separated from the undesired isomeric chloride by frac-tional crystallization from mixtures of polar and non-polar 1~9~3~
organic solvents such as mixtures of diethyl ether and petroleum ether, and acetone or ethyl acetate mixed with hexane or petroleum ether.
The 1,3-disubstituted ureas are prepared by well known methods or are commercially available.
Illustrative N-substituted-aminocarbonyl-N-methyl-carbamoyl chlorides are represented by the foregoing formula wherein R" is ethyl, H2C=CH-CH2-(allyl), HC-C-CH2-(propargyl), phenyl, benzyl, 2-furfuryl, cyclopropyl and cyclohexyl.
The cyclic ureido carbamoyl chlorides Il o Y-N ~~C-CI
(CH~)n wherein Y and n are as defined above are prepared by react-ing the substituted (Y=acetyl or methylsulfonyl) or unsubsti-tuted (Y=H), imidazolidine-2-one(n=2) or hexahydropyrimidine-
2-one(n=3) with phosgene in a dry, inert solvent at about 0-10C.
The cyclic ureido carbamoyl chlorides used to prepare the cephalosporins of the formula I are imidazol-idine-2-one-1-ylcarbonyl chloride, 3-(methylsulfonyl)-imidazolidine-2-one-1-ylcarbonyl chloride, hexahydropyrimidino-2-one-1-ylcarbonyl chloride, 3-(methylsulfonyl)hexahydropyrimi-dine-2-one-1-yl-carbonyl chloride, and 3-(acetyl)hexahydro-pyrimidine-2-one-1-ylcarbonyl chloride.
The preparation of the compounds represented by 1~9~i37~
the formula I wherein R3 is hydrogen and R' is CH3 is illus-trated by the following description of the preparation of 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-phenylacet-amido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid. 7-(D--Amino-a-phenylacetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid is suspended in acetonitrile containing an excess of propylene oxide. A small excess of bis-(trimethylsilyl)-acetamide is added to the suspension with stirring to effect solution. The solution is cooled to about 5C. and a molar equivalent of N-methylaminocarbonyl-N-methylcarbamoyl chlor-ide is added dropwise or portionwise with stirring. After stirring for about 2-4 hours in the cold, the reaction mixture is allowed to warm to room temperature. The product is preferably isolated via extraction with an organic sol-vent such as ethyl acetate. The reaction mixture is poured i~,o a mixture of ethyl acetate and water, the aqueous phase ;3 separated, acidified, and the product extracted with ethyl acetate.
The compounds of the formula I wherein R' is hydrogen are prepared by acylating the ~-amino cephalosporin starting material II with a p-nitrophenyl carbamate R' ' -N-C-N-C-O--~ >--NO2 wherein R" has the previously defined meanings. These esters are prepared by reacting urea or the mono-substituted urea, ~-4087A 12 ~' ~96373 R"-NH-C(O)-NH2 in an inert solvent such as THF with p-nitro-phenyl chloroformate. For example, methylurea is reacted in dry THF at about 0C. with p-nitrophenyl chloroformate to form p-nitrophenyl N-(methylcarbamoyl)carbamate.
As is the case in the preparation of the above described carbamoyl chlorides, the reaction of urea or a mono-substituted urea with p-nitrophenyl chloroformate affords two isomeric p-nitrophenyl carbamates.
The desired carbamate is formed by the acylation of the Nl(unsubstituted)urea nitrogen while the undesired carbamate ester is fo~med by the acylation of the N3(sub-stituted), or the R"-N-, urea nitrogen. Usually the two products are formed in equal amounts.
The desired p-nitrophenyl N-(substituted carbamoyl) carbamates form isocyanates when treated with silylating agents such as bis-(trimethylsilyl)acetamide (BSA) or mono-(trimethylsilyl)acetamide (MSA). The reaction is illus-trated by the scheme:
H 0 H 0 ._ H 0 1 11 1 11 ~ ~ 1 11 R''-N-C-N-C-0~ -N02 BSA ~ R''-N~C-N=C=0 -- +
H0~ -N02 The undesired p-nitrophenyl carbamate ~6373 R' '-N-C-NH2 C=O
o~ -NO2 .
formed along with the above desired carbamate is incapable of forming an isocyanate with the silylating agent.
In the acylation of an a-aminoarylacetamido cephalosporin, II, to form the cephalosporin I wherein R'=H, the mixture of both carbamates obtained as described above is conveniently used. The acylation reaction is carried out in an inert dry solvent in the presence of an excess of a silylating agent such as BSA or MSA. The p-nitrophenyl N-(substituted carbamoyl)carbamate forms the isocyanate ln situ which then reacts with the ~-amino group of II to form the product.
Illustrative p-nitrophenyl carbamates useful in preparing the compounds of the formula I wherein R'=H are p-nitrophenyl N-(ethylcarbamoyl)carbamate, p-nitrophenyl N-tcyclopropylcarbamoyl)carbamate, p-nitrophenyl N-(phenyl-carbamoyl)carbamate, p-nitrophenyl N-(phenylcarbamoyl)-carbamate, p-nitrophenyl N-(propargylcarbamoyl)carbamate, p-nitrophenyl N-(allylcarbamoyl)carbamate, p-nitrophenyl N-(benzylcarbamoyl)carbamate and p-nitrophenyl N-(carbamoyl)-carbamate (R"=H).
The acylation of an a-aminoarylacetamido cephalo-sporin, II, with the above p-nitrophenyl carbamates is conveniently carried out in dry acetonitrile at about room temperature (20-25C.). Ir. order to insure anhydrous condi-tions the acylation is preferably carried out in an atmos-X-~087A 14 ~9~3q3~
phere of a dry inert gas such as nitrogen or argon. A sily-lating agent such as BSA or MSA is added in excess and serves two functions. It first serves to solubilize the -aminoarylacetamidocephalosporin II via formation of solu-ble silyl derlvatives (for example a silyl ester of II) and secondly the excess reacts with the p-nitrophenyl carbamate to generate, in situ, the isocyanate as described above.
. .
The acylation reaction is carried out as follows.
A suspension of the a-aminoarylacetamido-cephalosporin II, in dry acetonitrile is treated with excess BSA. After a homogeneous solution is obtained the mixture of p-nitro-phenyl carbamates is added in an amount sufficient to provide at least one molar equivalent of the desired p-nitrophenyl carbamate isomer per compound II.
The reaction mixture is stirred at room tempera-ture for between 1 and 3 hours after which the product is recovered.
The cephalosporin product (formula I, R'=H, R3=H) is conveniently recovered by extracting the reaction mixture, after dilution with water, with a water-immiscible organic solvent such as ethyl acetate, amyl acetate or other suit-able solvent. The extraction is carried out at acid pH and ' preferably at about pH 2.5. The extract is washed, dried and evaporated to yield the cephalosporin antibiotic of the invention.
In an exemplary preparation of the cephalosporins of the formula I wherein R' is hydrogen, 7-[a-amino-a-(2-thienyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthio-methyl)-3-cephem-4-carboxylic acid is reacted in dry aceton-itrile in the presence of excess bis-(trimethylsilyl)-1~963~73 acetamide with p-nitrobenzyl N-(methylcarbamoyl)carbamate to provide, after recovery, 7-[a-(3-methylcarbamoyl-1-ureido)-~-(2-thienyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-yl-thiomethyl)-3-cephem-4-carboxylic acid.
According to the above described preparative procedures the compounds of the formula I wherein R is a 1,3-disubstituted ureido group of the formula H O
R' '-N-C-N- (R'=CH3) are prepared with the above described carbamoyl chlorides.
The compounds I, wherein R' is hydrogen, are prepared as described above with a p-nitrophenyl N-(substituted carba-moyl) carbamate, H O H O
I 11 1 11 ~ ~
R''-N-C-N-C-0--~ / -N02 Illustrative of the cephalosporin antibiotics of the formula I wherein R3 is hydrogen are the following.
1~6.~73 R Rl R2 CH3N-C-N- phenyl -S~
4-hydroxy- CH3 do phenyl do 4-chloro-do phenyl do 4-hydroxy-
The cyclic ureido carbamoyl chlorides used to prepare the cephalosporins of the formula I are imidazol-idine-2-one-1-ylcarbonyl chloride, 3-(methylsulfonyl)-imidazolidine-2-one-1-ylcarbonyl chloride, hexahydropyrimidino-2-one-1-ylcarbonyl chloride, 3-(methylsulfonyl)hexahydropyrimi-dine-2-one-1-yl-carbonyl chloride, and 3-(acetyl)hexahydro-pyrimidine-2-one-1-ylcarbonyl chloride.
The preparation of the compounds represented by 1~9~i37~
the formula I wherein R3 is hydrogen and R' is CH3 is illus-trated by the following description of the preparation of 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-phenylacet-amido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid. 7-(D--Amino-a-phenylacetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid is suspended in acetonitrile containing an excess of propylene oxide. A small excess of bis-(trimethylsilyl)-acetamide is added to the suspension with stirring to effect solution. The solution is cooled to about 5C. and a molar equivalent of N-methylaminocarbonyl-N-methylcarbamoyl chlor-ide is added dropwise or portionwise with stirring. After stirring for about 2-4 hours in the cold, the reaction mixture is allowed to warm to room temperature. The product is preferably isolated via extraction with an organic sol-vent such as ethyl acetate. The reaction mixture is poured i~,o a mixture of ethyl acetate and water, the aqueous phase ;3 separated, acidified, and the product extracted with ethyl acetate.
The compounds of the formula I wherein R' is hydrogen are prepared by acylating the ~-amino cephalosporin starting material II with a p-nitrophenyl carbamate R' ' -N-C-N-C-O--~ >--NO2 wherein R" has the previously defined meanings. These esters are prepared by reacting urea or the mono-substituted urea, ~-4087A 12 ~' ~96373 R"-NH-C(O)-NH2 in an inert solvent such as THF with p-nitro-phenyl chloroformate. For example, methylurea is reacted in dry THF at about 0C. with p-nitrophenyl chloroformate to form p-nitrophenyl N-(methylcarbamoyl)carbamate.
As is the case in the preparation of the above described carbamoyl chlorides, the reaction of urea or a mono-substituted urea with p-nitrophenyl chloroformate affords two isomeric p-nitrophenyl carbamates.
The desired carbamate is formed by the acylation of the Nl(unsubstituted)urea nitrogen while the undesired carbamate ester is fo~med by the acylation of the N3(sub-stituted), or the R"-N-, urea nitrogen. Usually the two products are formed in equal amounts.
The desired p-nitrophenyl N-(substituted carbamoyl) carbamates form isocyanates when treated with silylating agents such as bis-(trimethylsilyl)acetamide (BSA) or mono-(trimethylsilyl)acetamide (MSA). The reaction is illus-trated by the scheme:
H 0 H 0 ._ H 0 1 11 1 11 ~ ~ 1 11 R''-N-C-N-C-0~ -N02 BSA ~ R''-N~C-N=C=0 -- +
H0~ -N02 The undesired p-nitrophenyl carbamate ~6373 R' '-N-C-NH2 C=O
o~ -NO2 .
formed along with the above desired carbamate is incapable of forming an isocyanate with the silylating agent.
In the acylation of an a-aminoarylacetamido cephalosporin, II, to form the cephalosporin I wherein R'=H, the mixture of both carbamates obtained as described above is conveniently used. The acylation reaction is carried out in an inert dry solvent in the presence of an excess of a silylating agent such as BSA or MSA. The p-nitrophenyl N-(substituted carbamoyl)carbamate forms the isocyanate ln situ which then reacts with the ~-amino group of II to form the product.
Illustrative p-nitrophenyl carbamates useful in preparing the compounds of the formula I wherein R'=H are p-nitrophenyl N-(ethylcarbamoyl)carbamate, p-nitrophenyl N-tcyclopropylcarbamoyl)carbamate, p-nitrophenyl N-(phenyl-carbamoyl)carbamate, p-nitrophenyl N-(phenylcarbamoyl)-carbamate, p-nitrophenyl N-(propargylcarbamoyl)carbamate, p-nitrophenyl N-(allylcarbamoyl)carbamate, p-nitrophenyl N-(benzylcarbamoyl)carbamate and p-nitrophenyl N-(carbamoyl)-carbamate (R"=H).
The acylation of an a-aminoarylacetamido cephalo-sporin, II, with the above p-nitrophenyl carbamates is conveniently carried out in dry acetonitrile at about room temperature (20-25C.). Ir. order to insure anhydrous condi-tions the acylation is preferably carried out in an atmos-X-~087A 14 ~9~3q3~
phere of a dry inert gas such as nitrogen or argon. A sily-lating agent such as BSA or MSA is added in excess and serves two functions. It first serves to solubilize the -aminoarylacetamidocephalosporin II via formation of solu-ble silyl derlvatives (for example a silyl ester of II) and secondly the excess reacts with the p-nitrophenyl carbamate to generate, in situ, the isocyanate as described above.
. .
The acylation reaction is carried out as follows.
A suspension of the a-aminoarylacetamido-cephalosporin II, in dry acetonitrile is treated with excess BSA. After a homogeneous solution is obtained the mixture of p-nitro-phenyl carbamates is added in an amount sufficient to provide at least one molar equivalent of the desired p-nitrophenyl carbamate isomer per compound II.
The reaction mixture is stirred at room tempera-ture for between 1 and 3 hours after which the product is recovered.
The cephalosporin product (formula I, R'=H, R3=H) is conveniently recovered by extracting the reaction mixture, after dilution with water, with a water-immiscible organic solvent such as ethyl acetate, amyl acetate or other suit-able solvent. The extraction is carried out at acid pH and ' preferably at about pH 2.5. The extract is washed, dried and evaporated to yield the cephalosporin antibiotic of the invention.
In an exemplary preparation of the cephalosporins of the formula I wherein R' is hydrogen, 7-[a-amino-a-(2-thienyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthio-methyl)-3-cephem-4-carboxylic acid is reacted in dry aceton-itrile in the presence of excess bis-(trimethylsilyl)-1~963~73 acetamide with p-nitrobenzyl N-(methylcarbamoyl)carbamate to provide, after recovery, 7-[a-(3-methylcarbamoyl-1-ureido)-~-(2-thienyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-yl-thiomethyl)-3-cephem-4-carboxylic acid.
According to the above described preparative procedures the compounds of the formula I wherein R is a 1,3-disubstituted ureido group of the formula H O
R' '-N-C-N- (R'=CH3) are prepared with the above described carbamoyl chlorides.
The compounds I, wherein R' is hydrogen, are prepared as described above with a p-nitrophenyl N-(substituted carba-moyl) carbamate, H O H O
I 11 1 11 ~ ~
R''-N-C-N-C-0--~ / -N02 Illustrative of the cephalosporin antibiotics of the formula I wherein R3 is hydrogen are the following.
1~6.~73 R Rl R2 CH3N-C-N- phenyl -S~
4-hydroxy- CH3 do phenyl do 4-chloro-do phenyl do 4-hydroxy-
3-chloro-do phenyl do do 2-thienyl do do 2-furyl do do 3-thienyl do do phenyl -S-~ -CH3
4-hydroxy-do phenyl do do 2-thienyl do H~ phenyl -S-~
3-hydroxy- CH3 do phenyl do do 2-thienyl do 3-chloro-do phenyl do do phenyl do 4-hydroxy-do phenyl do 1~39~Y~3 H~ phenyl_s_~\ ~-CH3 3-chloro-4-hydroxy--do phenyl do do 2-thienyl do do 2-furyl do do phenylacetoxy 4-hydroxy-do phenyl do do 2-thienyl do O ~ .
CH3-C-N \~- phenyl acetoxy 4-hydroxy-do phenyl 20CH3-SO2-~ phenyl do do 2-thienyl do do 2-furyl do CH3-SO2-~ 1- phenyl do \~/
~L~ ~3~;3~7 3 R Rl R2 do do acetoxy 4-hydroxy-do phenyl do H do do ~ ~~
CH3-N-C-N- phenyl acetoxy 4-hydroxy-do phenyl do 3-chloro-4-hydroxy-do phenyl do do 2-thienyl do R''-N-C-N~
R' (R") (R') ~ _ ~
phenyl H phenyl --~\/Y CH3 do CH3 do acetoxy benzyl H do ~
4-hydroxy-2-furfuryl H phenyl do allyl H phenyl do do CH3 do acetoxy ~9~373 R Rl R2 (R") (R') 3-chloro-4-hydroxy-propargyl H phenyl do do H 2-thienyl do do CH3 do ~
do H phenyl do cyclo-propyl H do do do H do acetoxy do CH3 do do cyclo-pentyl H do do 4-chloro- N N
do H phenyl \S/
4-hydroxy-do H phenyl do do CH3 phenyl 1~9637'3 The cephalosporin antibiotics of the formula I
wherein R3 is hydrogen are converted to the acyloxymethyl esters, wherein R3 is represented by the group O
-CH2-O-C-Y' by reacting an alkali metal salt of the cephalosporin car-boxylic acid, for example, the lithium, sodium, or potassium ; salt, with an acyloxymethyl halide of the formula O
X-CH2-O-C-Y' wherein X is chloro or bromo and Y' has the same meanings as previously defined. Acyloxymethyl halides which can be ; employed include chloromethyl acetate, bromomethyl acetate, bromomethyl propionate, chloromethyl pivaloate, and benzo-yloxymethyl chloride.
The preparation of the acyloxymethyl esters of the formula I is carried out by reacting the alkali metal salt form of the parent acid in an inert solvent with a slight molar excess of the bromo or ch]oromethyl ester, e.g., bromomethyl acetate at room temperature or at slightly elevated temperatures up to about 40-45C. Solvents such as acetone, tetrahydrofuran, dioxane, dimethylformamide, and methylene chloride can be used.
The indanyl esters of the formula I wherein R3 is ~C~9G373 1 `
are prepared by reacting 5-indanol in an inert solvent such as dioxane or tetrahydrofuran with the free acid form of a compound of the formula I wherein R3 is hydrogen, in the presence of a condensing agent such as a diimide, for example, dicyclohexyldiimide. T~e reaction is carried out with stirring at about 20-35C. for about 6 to 8 hours. The indanyl ester is isolated by first diluting the reaction mixture with water and filtering the reaction mixtu~ to remove the insoluble dicyclohexylurea. The ester is then extracted from the filtrate.
Alternatively, the indanyl esters can be prepared by reacting a mixed acid anhydride formed with a cephalo-sporin acid of the formula I and acetic acid with 5-indanol.
The phthalidyl esters of the formula I wherein R3 is the phthalidyl group 63~73 are obtained by reacting bromopht:halide of t-he Eormula with a salt of a cephalosporin acid of the formula I. The esterification can be carried out in dimethylformamide, dimethylacetamide, dioxane, tetrahydrofuran, or mixtures thereof by slowly warming a mixture of equimolar amounts of the cephalosporin acid salt, for example, the sodium or potassium salt and bromophthalide.
I~lustrative esters of the formula I are:
acetoxymethyl 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)--phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl)-3-cephem-4-carboxylate;
pivaloyloxymethyl 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido]-a-(4-hydroxyphenyl)acetamido]-3-t5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylate;
phthalidyl 7-[a-(3-methylaminocarbamoyl-3-methyl-l-ureido)--phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylate;
acetoxymethyl 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(3-chloro-4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylate;
1~ 373 acetoxy~ethyl 7-[~-(3-methylcarbamoyl-1-ureido)-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl)-3-cephem-4-carboxylate; and pivaloyloxymethyl 7-[~-(3-methylcarbamoyl-1-ureido)-~-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylate.
The cephalosporin compounds of this invention, in the free acid form (formula I, R3=H), form pharmaceutically acceptable salts with inorganic bases such as the alkali metal carbonates and bicarbonates. For example, the sodium and potassium salts can be formed with sodium and potassium carbonate by following conventional procedures.
Salts can also be prepared with basic organic amines, such as methylamine, diethylamine, cyclohexylamine, dicyclohexylamine, ethanol amine, diethanol amine, and tris-~hydroxymethyl)aminomethane. Such salts can be used to formulate the antibiotics into suitable pharmaceutical forms for parenteral administraticn.
The cephalosporin antibiotics of this invention are highly effective in inhibiting the growth of a wide spectrum of pathogenic microorganisms of both the gram-positive and gram-negative type.
A number of cephalosporin antibiotics are known which are effective against gram-positive microorganisms but are limited in the spectrum of activity against the gram-negative microorganisms. Other cephalosporin antibiotics which have been synthesized have demonstrated enhanced gram-negative activity; however, they possess either a lower spectrum of activity against the gram-positive organisms 1~963~73 or a decreased level of activity against these organisms.
The antibiotics described herein ~have enhanced gram-negative activity both with respect to spectrum and level of activity as well as activity against the gram-positive microorganisms.
Thus, the antibiotics described herein can be characterized as cephalosporins having an expanded spectrum of activity.
These cephalosporin antibiotics exhibit high levels of activity against -the Pseudomonas, Enterobacter sp., indole (+) and (-), Pro-teus sp., Aerobacter, Serratia, and Klebsiella gram-negative microorganisms. They also are effective in controlling the growth of penicillin resistant Staphylococcus as well as the Streptococcus D group, e.g., S. faecalis.
The antibiotic activity of the cephalosporin compounds of the formula I is illustrated by the data pre-sented in Table I for representative compounds. The values in the table are the minimum inhibitory concentrations (MIC) for the test compounds against the indicated microorganisms.
The MIC values were obtained in the Gradient Plate ln vitro method for determining antibiotic activity.
1~9~373 Z
H ^ 1:'~ ~ ~ ~ ~ ~1 N ~ 0 O ~i ~ (~
P~ ~ A
V~
O
o ) ~ o ~ ~ ~ ~ n o o C) ~ N
O
o a ~ ~ 1-- ~ ~ O O ~D ,~ O O
m ~ ~
H :~ O U~
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~9~373 A. 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl) 3-cephem-4-carboxylic acid.
B. 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid.
C. 7-[a-(3-methylcarbamoyl-3-methyl-1 ureido)-a-phenylacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid.
D. 7-[a-(imidazolidine-2-one-1-ylcarbonylamino)-a-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
E. 7-[a-(imidazclidine-2-one-1-ylcarbonylamino)-a-phenylacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid.
F. 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-phenyl-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
H. 7-[a-(3-carbamoyl-1-ureido-a-phenylacetamido]-3-(l-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
I. 7-[a-(3-methylcarbamoyl-1-ureido)-a-(2-thienyl)-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
J. 7-[a-(3-methylcarbamoyl-1-ureido)-a-phenylacetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-car-boxylic acid.
K. 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl)-3-cephem-4-carboxylic acid.
L. Sodium 7-la-(3-methylcarbamoyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-yl-'1~9~i373 thiomethyl)3-cephem-4-carboxylat:e.
M. 7-[~-(3-phenylcarbamoyl-1-ureido)-~-phenylace-tamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
In the standard agar dilution method, the MIC
values for the above test compounds A through E against Staphylococcus aureus were as follows: A, 2; B, l; C, 0.5;
. . .
D, 2; and E, 0.5 mcg./ml.
The cephalosporin antibiotics of the formula I, wherein R3 is hydrogen, and the pharmaceutically acceptable salts thereof are useful in combating infections in warm blooded mammals when administered parenterally in non-toxic doses between about 10 and 500 mg./kg. The indanyl, phthal-idyl and acyloxymethyl esters of the formula I are useful antibiotics when administered orally in non-toxic doses of between about 50 and 750 mg./kg. of body weight.
A preferred group of cephalosporin antibiotics of this invention are represented by the formula I wherein R is CH~-N-C-N- or H-N \N-H R ~
R' is H or methyl;
Rl is phenyl, hydroxyphenyl, hydroxy-substituted halo-phenyl, or 2-thienyl;
R2 iS
~96,3~3 -S-~
R3 is hydrogen and the pharmaceutically acceptable salts thereof.
A further preferred group of antibiotics are represented by the formula I when R is H R' R' is hydrogen or methyl;
Rl is phenyl, hydroxyphenyl, or hydroxy substituted halophenyl or 2-thienyl;
R2 iS
\S
R3 is hydrogen and the pharmaceutically acceptable non-toxic salts thereof.
Exemplary of the preferred antibiotics are 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-phenylacetamido]-3-(1-1~9~i3'73 methyl-lH-tetrazole-5-ylthiomethyl)--3-cephem-4-carboxylie acid, 7-[~-(3-methylcarbamoyl-3--methyl-1-ureido)-~-(4-hydroxyphenyl)aeetamido]-3-(S-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid;
7-[~-(3-methylcarbamoyl-3--methyl-1-ureido)--(4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-2-ylthiomethyl)-3-eephem-4-carboxylic acid, 7-[~-(3-methylcarbamoyl-1-ureido)-~-phenylacet-amido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid, 7-[~-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-earboxylie acid, 7-[-(3-methylearbamoyl-1-ureido)-a-(2-thienyl)-aeetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl-3-cephem-4-earboxylie aeid.
7-[~-(imidazolidine-2-one-1-ylearbonylamino)-~-phenylaeetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-eephem-4-earboxylie aeid, 7-[a-(3-methylearbamoyl-3-methyl-1-ureido)-~-(3-chloro-4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-
3-hydroxy- CH3 do phenyl do do 2-thienyl do 3-chloro-do phenyl do do phenyl do 4-hydroxy-do phenyl do 1~39~Y~3 H~ phenyl_s_~\ ~-CH3 3-chloro-4-hydroxy--do phenyl do do 2-thienyl do do 2-furyl do do phenylacetoxy 4-hydroxy-do phenyl do do 2-thienyl do O ~ .
CH3-C-N \~- phenyl acetoxy 4-hydroxy-do phenyl 20CH3-SO2-~ phenyl do do 2-thienyl do do 2-furyl do CH3-SO2-~ 1- phenyl do \~/
~L~ ~3~;3~7 3 R Rl R2 do do acetoxy 4-hydroxy-do phenyl do H do do ~ ~~
CH3-N-C-N- phenyl acetoxy 4-hydroxy-do phenyl do 3-chloro-4-hydroxy-do phenyl do do 2-thienyl do R''-N-C-N~
R' (R") (R') ~ _ ~
phenyl H phenyl --~\/Y CH3 do CH3 do acetoxy benzyl H do ~
4-hydroxy-2-furfuryl H phenyl do allyl H phenyl do do CH3 do acetoxy ~9~373 R Rl R2 (R") (R') 3-chloro-4-hydroxy-propargyl H phenyl do do H 2-thienyl do do CH3 do ~
do H phenyl do cyclo-propyl H do do do H do acetoxy do CH3 do do cyclo-pentyl H do do 4-chloro- N N
do H phenyl \S/
4-hydroxy-do H phenyl do do CH3 phenyl 1~9637'3 The cephalosporin antibiotics of the formula I
wherein R3 is hydrogen are converted to the acyloxymethyl esters, wherein R3 is represented by the group O
-CH2-O-C-Y' by reacting an alkali metal salt of the cephalosporin car-boxylic acid, for example, the lithium, sodium, or potassium ; salt, with an acyloxymethyl halide of the formula O
X-CH2-O-C-Y' wherein X is chloro or bromo and Y' has the same meanings as previously defined. Acyloxymethyl halides which can be ; employed include chloromethyl acetate, bromomethyl acetate, bromomethyl propionate, chloromethyl pivaloate, and benzo-yloxymethyl chloride.
The preparation of the acyloxymethyl esters of the formula I is carried out by reacting the alkali metal salt form of the parent acid in an inert solvent with a slight molar excess of the bromo or ch]oromethyl ester, e.g., bromomethyl acetate at room temperature or at slightly elevated temperatures up to about 40-45C. Solvents such as acetone, tetrahydrofuran, dioxane, dimethylformamide, and methylene chloride can be used.
The indanyl esters of the formula I wherein R3 is ~C~9G373 1 `
are prepared by reacting 5-indanol in an inert solvent such as dioxane or tetrahydrofuran with the free acid form of a compound of the formula I wherein R3 is hydrogen, in the presence of a condensing agent such as a diimide, for example, dicyclohexyldiimide. T~e reaction is carried out with stirring at about 20-35C. for about 6 to 8 hours. The indanyl ester is isolated by first diluting the reaction mixture with water and filtering the reaction mixtu~ to remove the insoluble dicyclohexylurea. The ester is then extracted from the filtrate.
Alternatively, the indanyl esters can be prepared by reacting a mixed acid anhydride formed with a cephalo-sporin acid of the formula I and acetic acid with 5-indanol.
The phthalidyl esters of the formula I wherein R3 is the phthalidyl group 63~73 are obtained by reacting bromopht:halide of t-he Eormula with a salt of a cephalosporin acid of the formula I. The esterification can be carried out in dimethylformamide, dimethylacetamide, dioxane, tetrahydrofuran, or mixtures thereof by slowly warming a mixture of equimolar amounts of the cephalosporin acid salt, for example, the sodium or potassium salt and bromophthalide.
I~lustrative esters of the formula I are:
acetoxymethyl 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)--phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl)-3-cephem-4-carboxylate;
pivaloyloxymethyl 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido]-a-(4-hydroxyphenyl)acetamido]-3-t5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylate;
phthalidyl 7-[a-(3-methylaminocarbamoyl-3-methyl-l-ureido)--phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylate;
acetoxymethyl 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(3-chloro-4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylate;
1~ 373 acetoxy~ethyl 7-[~-(3-methylcarbamoyl-1-ureido)-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl)-3-cephem-4-carboxylate; and pivaloyloxymethyl 7-[~-(3-methylcarbamoyl-1-ureido)-~-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylate.
The cephalosporin compounds of this invention, in the free acid form (formula I, R3=H), form pharmaceutically acceptable salts with inorganic bases such as the alkali metal carbonates and bicarbonates. For example, the sodium and potassium salts can be formed with sodium and potassium carbonate by following conventional procedures.
Salts can also be prepared with basic organic amines, such as methylamine, diethylamine, cyclohexylamine, dicyclohexylamine, ethanol amine, diethanol amine, and tris-~hydroxymethyl)aminomethane. Such salts can be used to formulate the antibiotics into suitable pharmaceutical forms for parenteral administraticn.
The cephalosporin antibiotics of this invention are highly effective in inhibiting the growth of a wide spectrum of pathogenic microorganisms of both the gram-positive and gram-negative type.
A number of cephalosporin antibiotics are known which are effective against gram-positive microorganisms but are limited in the spectrum of activity against the gram-negative microorganisms. Other cephalosporin antibiotics which have been synthesized have demonstrated enhanced gram-negative activity; however, they possess either a lower spectrum of activity against the gram-positive organisms 1~963~73 or a decreased level of activity against these organisms.
The antibiotics described herein ~have enhanced gram-negative activity both with respect to spectrum and level of activity as well as activity against the gram-positive microorganisms.
Thus, the antibiotics described herein can be characterized as cephalosporins having an expanded spectrum of activity.
These cephalosporin antibiotics exhibit high levels of activity against -the Pseudomonas, Enterobacter sp., indole (+) and (-), Pro-teus sp., Aerobacter, Serratia, and Klebsiella gram-negative microorganisms. They also are effective in controlling the growth of penicillin resistant Staphylococcus as well as the Streptococcus D group, e.g., S. faecalis.
The antibiotic activity of the cephalosporin compounds of the formula I is illustrated by the data pre-sented in Table I for representative compounds. The values in the table are the minimum inhibitory concentrations (MIC) for the test compounds against the indicated microorganisms.
The MIC values were obtained in the Gradient Plate ln vitro method for determining antibiotic activity.
1~9~373 Z
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~9~373 A. 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl) 3-cephem-4-carboxylic acid.
B. 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid.
C. 7-[a-(3-methylcarbamoyl-3-methyl-1 ureido)-a-phenylacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid.
D. 7-[a-(imidazolidine-2-one-1-ylcarbonylamino)-a-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
E. 7-[a-(imidazclidine-2-one-1-ylcarbonylamino)-a-phenylacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid.
F. 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-phenyl-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
H. 7-[a-(3-carbamoyl-1-ureido-a-phenylacetamido]-3-(l-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
I. 7-[a-(3-methylcarbamoyl-1-ureido)-a-(2-thienyl)-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
J. 7-[a-(3-methylcarbamoyl-1-ureido)-a-phenylacetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-car-boxylic acid.
K. 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl)-3-cephem-4-carboxylic acid.
L. Sodium 7-la-(3-methylcarbamoyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-yl-'1~9~i373 thiomethyl)3-cephem-4-carboxylat:e.
M. 7-[~-(3-phenylcarbamoyl-1-ureido)-~-phenylace-tamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
In the standard agar dilution method, the MIC
values for the above test compounds A through E against Staphylococcus aureus were as follows: A, 2; B, l; C, 0.5;
. . .
D, 2; and E, 0.5 mcg./ml.
The cephalosporin antibiotics of the formula I, wherein R3 is hydrogen, and the pharmaceutically acceptable salts thereof are useful in combating infections in warm blooded mammals when administered parenterally in non-toxic doses between about 10 and 500 mg./kg. The indanyl, phthal-idyl and acyloxymethyl esters of the formula I are useful antibiotics when administered orally in non-toxic doses of between about 50 and 750 mg./kg. of body weight.
A preferred group of cephalosporin antibiotics of this invention are represented by the formula I wherein R is CH~-N-C-N- or H-N \N-H R ~
R' is H or methyl;
Rl is phenyl, hydroxyphenyl, hydroxy-substituted halo-phenyl, or 2-thienyl;
R2 iS
~96,3~3 -S-~
R3 is hydrogen and the pharmaceutically acceptable salts thereof.
A further preferred group of antibiotics are represented by the formula I when R is H R' R' is hydrogen or methyl;
Rl is phenyl, hydroxyphenyl, or hydroxy substituted halophenyl or 2-thienyl;
R2 iS
\S
R3 is hydrogen and the pharmaceutically acceptable non-toxic salts thereof.
Exemplary of the preferred antibiotics are 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-phenylacetamido]-3-(1-1~9~i3'73 methyl-lH-tetrazole-5-ylthiomethyl)--3-cephem-4-carboxylie acid, 7-[~-(3-methylcarbamoyl-3--methyl-1-ureido)-~-(4-hydroxyphenyl)aeetamido]-3-(S-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid;
7-[~-(3-methylcarbamoyl-3--methyl-1-ureido)--(4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-2-ylthiomethyl)-3-eephem-4-carboxylic acid, 7-[~-(3-methylcarbamoyl-1-ureido)-~-phenylacet-amido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid, 7-[~-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-earboxylie acid, 7-[-(3-methylearbamoyl-1-ureido)-a-(2-thienyl)-aeetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl-3-cephem-4-earboxylie aeid.
7-[~-(imidazolidine-2-one-1-ylearbonylamino)-~-phenylaeetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-eephem-4-earboxylie aeid, 7-[a-(3-methylearbamoyl-3-methyl-1-ureido)-~-(3-chloro-4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-
5-ylthiomethyl)-3-eephem-4-earboxylie aeid.
7-1~-(3-methylearbamoyl-3-methyl-1-ureido)-~-(3,5-diehloro-4-hydroxyphenyl)aeetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-eephem-4-earboxylie aeid, and the pharma-eeutieally aeeeptable, non-toxie salts thereof.
The in vivo effeetive dose (ED50) in mg./kg. for representative antibioties of the formula I has been deter-mined in experimental infeetions in miee. Table II lists 63'73 the ED50 dose vs Streptococcus ~ogenes and Escherichia coli infections. In the table, the antibiotics are identified with the R", R', and Rl-R3 terms of Formula I.
1~963~73 TABLE II
Test Compound ED50(mg/kg x 2) i.p.
R" R' R R R S. pyogenes E. coli ~ 2 3 --CH3 H phenyl tet H 0.7 72 4-hydroxy CH3 CH3 phenyl tet H 0.7 72 H H phenyl tet H 0.7 <72 4-hydroxy 2 CH3 H phenyl thiad H 0.7 <72 CH3 H 2-thienyl tet H ~7.2 <72 CH3 CH3 phenyl acetoxy H<7.2 ~7.2 l/tet=l-methyl-lH-tetrazole-5-ylthio-2/thiad=5-methyl-1,3,4-thiadiazole-2-ylthio-, ~96373 The following examples are provided to further describe this invention and are not to be construed as limiting thereof.
In the examples the following abbreviations have the meaning indicated below.
BSA - bis-(trimethylsilyl)acetamide THS - tetrahydrofuran DMF - dimethylformamide NMR - nuclear magnetic resonance spectrum IR - infrared absorption spectrum UV - ultraviolet absorption spectrum.
Example 1 N-Methylcarbamoyl-N-methylcarbamoyl chloride.
To a cold suspension of 22 g. (0.25 m.) of sym-di-methylurea in dichloroethane was added dropwise with stirring a cold solution of 30 g. (0.3 m.) of phosgene in 90 ml. of dichloroethane. After the addition of the phosgene sclution was complete, the reaction mixture was allowed to stir at room temperature for one hour and was then heated to 80C.
and purged with nitrogen for one hour. The reaction mixture was evaporated under reduced pressure and the residual gum was extracted twice with 350 ml. portions of ether. The extracts were combined and evaporated to provide 25 g. of the carbamoyl chloride.
Example 2 Imidazolidine-2-one-1-ylcarbonyl chloride.
To a stirred suspension of 35 g. of 2-imidazolidine in 500 ml. of dry tetrahydrofuran cooled in an ice bath was added a cold solution of 40 g. of phosgene in 100 ml. of dry tetrahydrofuran. The reaction mixture was stirred at room ~963~3 temperature for about 16 hours and was filtered to remove insolubles. The filtrate was concentrated under reduced pressure and the reaction product precipitated from the concentrate on the addition of acetone and petroleum ether.
The product was collected by filtration and dried on the filter.
Example 3 Preparation of 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a suspension of 483 mg. (1 mmole) of 7-[D-a-amino--(4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 8 ml of dry acetonitrile containing 2 ml. of propylene oxide maintained under an atmosphere of dry argon was added 1 ml. of bis-ttri-methylsilyl)acetamide. When solution was obtained, the reaction vessel and solution were cooled to 0-5C. A solu-tion of 150 mg. (1 mmole) of N-methylaminocarbonyl-N~methyl-carbamoyl chloride in 2 ml. of dry acetonitrile was added dropwise to the cold solution with stirring. The reaction mixture was stirred for 2 hours and was allowed to warm to room temperature. The reaction mixture was poured into a mixture of water and ethyl acetate and the pH of the mixture was adjusted to pH 9. The aqueous layer was separated and relayered with fresh ethyl acetate. The pH of the aqueous layer was adjusted to pH 2.5 and the ethyl acetate layer was separated, was washed with brine and dried over sodium sulfate. The dried ethyl acetate solution containing the reaction product was evaporated to dryness in vacuo to obtain the product as a faintly yellow powder. The product was dissolved in ethyl acetate and in part precipitated by adding petroleum ether to the solution. The precipitate of product was filtered and dried to yield 138 mg. Additional product was recovered by evaporation of the filtrate.
NMR (60 MHz., DMSO d6): 9.8 (d, J=7, lH), 9.3 (d, J=8, lH), 7.4-6.5 (m, 5H), 5.85-5.50 (g, lH), 5.50-5.30 (d, J=7, lH), 4.9 (d, J=5, lH), 4.3 (broad, 2H), 3.5 (s, 3H), 3.6 (broad, 2H), 3.1 (s, 3H) and 2.65 (d, J=3, 3H) delta.
Elemental analysis (percent) for C22H25NgO7S2 Theory: C, 44.66; H, 4.26; N, 21.31 Found: C, 44.32; H, 4.34; N, 19.32.
Example 4 Preparation of 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a suspension of 2.12 g. (4 mmole) of 7-[D-a-amino-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thia-diazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid in 32 ml.
of dry acetonitrile containing 8 ml. of propylene oxide maintained under an atmosphere of dry argon was added 4 ml.
of bis-(trimethylsilyl)acetamide with stirring. When solu-tion had occurred, the solution was cooled to O~C. and 600 mg. (4 mmole) of N-methylaminocarbonyl-N-methylcarbamoyl chloride in 8 ml. of dry acetonitrile were added dropwise with stirring. The reaction mixture was stirred for 2 hours during which time the temperature of the mixture was allowed to rise to room temperature. The reaction mixture was poured into a water-ethyl acetate mixture and the pH of the g~,373 a~ueous layer was adjusted to pH 8.5. The aqueous layer was separated and layered with fresh ethyl acetate. The pH of the aqueous layer was then adjusted to about pH 2.5 and the ethyl acetate layer was separated, washed with brine and dried over sodium sulfate. The dried solution was evaporated to dryness under reduced pressure to yield about 1.6 g. of the product as a light yellow solid. The product ~as trit-urated with ethyl acetate and the insoluhle product (645 mg.) was filtered. The filtrate was concentrated by evapora-tion to yield 423 mg. of precipitated product. The latter filtrate was evaporated to dryness to yield 560 mg. The above three product fractions were shown to be the same when chromatographed on silica gel thin layer chromatograms using chloroform:methanol (7:3, v:v) for development and either iodine vapors or ultraviolet light for visualization of the developed plates.
Elemental analysis (percent) for C23H25N7O7S3:
Theory: C, 45.46; H, 4.15; N, 16.13 Found: C, 45.53; H, 4.47; N, 14.85.
Electrometric tritration in 66 percent DMF showed the presence of two titratable groups:
PKa 4.8 and 12.2 and an apparent molecular weight as calculated from the titration data of 587 (calculated MW=607). The infrared absorption spectrum (mineral oil mull) showing the character- -istic ~-lactam carbonyl absorption at about 2920 wave numbers and the NMR spectrum were in agreement with the expected product.
~96~7:~
UV absorption spectrum (methanol) A max 303 ~=9,246 max 275 ~=9,273 max 229 ~=16,254 Example 5 Preparation of 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-phenylacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid.
The above-named compound was ~repared by the reaction of 7-(D-a-amino-a-phenylacetamido)-3-acetoxymethyl-3-cephem-4-carboxylic acid (cephaloglycine) with N-methyl-aminocarbonyl-N-methylcarbamoyl chloride by following the reaction conditions employed in Example 3. The product (158 mg.) was obtained as a white crystalline solid.
Nuclear magnetic resonance spectrum (60 MHz., DMSO
d6): 7.45 (s, 5H), 5.9-5.4 (m, 2H), 5.2-4.4 tm, 3H) 3.5 ~broad, 2H), 3.15 (s, 3H), 2.7 (s, 3H) and 2.05 (s, 3H) delta.
Example 6 Preparation of 7-[D-a-(imidazolidine-2-one-1-ylcarbonyl-amino)-~-phenylacetamido]-3-acetoxymethyl-3-cephem-4-carboxy-lic ncid.
A suspension of 17.66 g. of cephaloglycine di-hydrate in 150 ml. of tetrahydrofuran-water (80 percent THF) was cooled in an ice bath and the pH of the suspension was adjusted to 7.8-8.2 by the addition of triethylamine. To the cold (0C.) suspension was added in small portions 5.94 g. of N-chlorocarbonylimidazolidine-2-one. Throughout the addition of the acid chloride, the pH of the reaction mixture was maintained between 7.5 and 8n 0 by adding triethylamine as required. Following the addition of the acid chloride, the reaction mixture was stirred at 0C. for 30 minutes and then at room temperature for another 20 minutes. The reaction mixture (pH 7.5) was diluted with 130 ml. of water and then evaporated to remove most of the THF. The aqueous phase was extracted once with ether and was then layered with ethyl acetate. The pH of the aqueous layer was adjusted to 1.5 to 2.0 with dilute hydrochloric acid. The ethyl acetate layer was separated and was washed with water and dried over magnesi~m sulfate. Evaporation of the dried ethyl acetate solution under reduced pressure provided the product as an amorphous solid.
Example 7 By following the acylation procedures and condi-tions described by Example 6, 7-(D--amino-a-phenylacetamido)-3-(1-methyl-lH-tetrazole-5~ylthiomethyl)-3-cephem-4-carboxy-lic acid is reacted with N-chlorocarbonylimidazolidine-2-one to provide 7-[D-(a-(imidazolidine-2-one-1-ylcarbonylamino)-a-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
Example 8 By following the procedures and by employing the solvents and conditions described in the acylation of Example
7-1~-(3-methylearbamoyl-3-methyl-1-ureido)-~-(3,5-diehloro-4-hydroxyphenyl)aeetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-eephem-4-earboxylie aeid, and the pharma-eeutieally aeeeptable, non-toxie salts thereof.
The in vivo effeetive dose (ED50) in mg./kg. for representative antibioties of the formula I has been deter-mined in experimental infeetions in miee. Table II lists 63'73 the ED50 dose vs Streptococcus ~ogenes and Escherichia coli infections. In the table, the antibiotics are identified with the R", R', and Rl-R3 terms of Formula I.
1~963~73 TABLE II
Test Compound ED50(mg/kg x 2) i.p.
R" R' R R R S. pyogenes E. coli ~ 2 3 --CH3 H phenyl tet H 0.7 72 4-hydroxy CH3 CH3 phenyl tet H 0.7 72 H H phenyl tet H 0.7 <72 4-hydroxy 2 CH3 H phenyl thiad H 0.7 <72 CH3 H 2-thienyl tet H ~7.2 <72 CH3 CH3 phenyl acetoxy H<7.2 ~7.2 l/tet=l-methyl-lH-tetrazole-5-ylthio-2/thiad=5-methyl-1,3,4-thiadiazole-2-ylthio-, ~96373 The following examples are provided to further describe this invention and are not to be construed as limiting thereof.
In the examples the following abbreviations have the meaning indicated below.
BSA - bis-(trimethylsilyl)acetamide THS - tetrahydrofuran DMF - dimethylformamide NMR - nuclear magnetic resonance spectrum IR - infrared absorption spectrum UV - ultraviolet absorption spectrum.
Example 1 N-Methylcarbamoyl-N-methylcarbamoyl chloride.
To a cold suspension of 22 g. (0.25 m.) of sym-di-methylurea in dichloroethane was added dropwise with stirring a cold solution of 30 g. (0.3 m.) of phosgene in 90 ml. of dichloroethane. After the addition of the phosgene sclution was complete, the reaction mixture was allowed to stir at room temperature for one hour and was then heated to 80C.
and purged with nitrogen for one hour. The reaction mixture was evaporated under reduced pressure and the residual gum was extracted twice with 350 ml. portions of ether. The extracts were combined and evaporated to provide 25 g. of the carbamoyl chloride.
Example 2 Imidazolidine-2-one-1-ylcarbonyl chloride.
To a stirred suspension of 35 g. of 2-imidazolidine in 500 ml. of dry tetrahydrofuran cooled in an ice bath was added a cold solution of 40 g. of phosgene in 100 ml. of dry tetrahydrofuran. The reaction mixture was stirred at room ~963~3 temperature for about 16 hours and was filtered to remove insolubles. The filtrate was concentrated under reduced pressure and the reaction product precipitated from the concentrate on the addition of acetone and petroleum ether.
The product was collected by filtration and dried on the filter.
Example 3 Preparation of 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a suspension of 483 mg. (1 mmole) of 7-[D-a-amino--(4-hydroxyphenyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 8 ml of dry acetonitrile containing 2 ml. of propylene oxide maintained under an atmosphere of dry argon was added 1 ml. of bis-ttri-methylsilyl)acetamide. When solution was obtained, the reaction vessel and solution were cooled to 0-5C. A solu-tion of 150 mg. (1 mmole) of N-methylaminocarbonyl-N~methyl-carbamoyl chloride in 2 ml. of dry acetonitrile was added dropwise to the cold solution with stirring. The reaction mixture was stirred for 2 hours and was allowed to warm to room temperature. The reaction mixture was poured into a mixture of water and ethyl acetate and the pH of the mixture was adjusted to pH 9. The aqueous layer was separated and relayered with fresh ethyl acetate. The pH of the aqueous layer was adjusted to pH 2.5 and the ethyl acetate layer was separated, was washed with brine and dried over sodium sulfate. The dried ethyl acetate solution containing the reaction product was evaporated to dryness in vacuo to obtain the product as a faintly yellow powder. The product was dissolved in ethyl acetate and in part precipitated by adding petroleum ether to the solution. The precipitate of product was filtered and dried to yield 138 mg. Additional product was recovered by evaporation of the filtrate.
NMR (60 MHz., DMSO d6): 9.8 (d, J=7, lH), 9.3 (d, J=8, lH), 7.4-6.5 (m, 5H), 5.85-5.50 (g, lH), 5.50-5.30 (d, J=7, lH), 4.9 (d, J=5, lH), 4.3 (broad, 2H), 3.5 (s, 3H), 3.6 (broad, 2H), 3.1 (s, 3H) and 2.65 (d, J=3, 3H) delta.
Elemental analysis (percent) for C22H25NgO7S2 Theory: C, 44.66; H, 4.26; N, 21.31 Found: C, 44.32; H, 4.34; N, 19.32.
Example 4 Preparation of 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a suspension of 2.12 g. (4 mmole) of 7-[D-a-amino-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thia-diazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid in 32 ml.
of dry acetonitrile containing 8 ml. of propylene oxide maintained under an atmosphere of dry argon was added 4 ml.
of bis-(trimethylsilyl)acetamide with stirring. When solu-tion had occurred, the solution was cooled to O~C. and 600 mg. (4 mmole) of N-methylaminocarbonyl-N-methylcarbamoyl chloride in 8 ml. of dry acetonitrile were added dropwise with stirring. The reaction mixture was stirred for 2 hours during which time the temperature of the mixture was allowed to rise to room temperature. The reaction mixture was poured into a water-ethyl acetate mixture and the pH of the g~,373 a~ueous layer was adjusted to pH 8.5. The aqueous layer was separated and layered with fresh ethyl acetate. The pH of the aqueous layer was then adjusted to about pH 2.5 and the ethyl acetate layer was separated, washed with brine and dried over sodium sulfate. The dried solution was evaporated to dryness under reduced pressure to yield about 1.6 g. of the product as a light yellow solid. The product ~as trit-urated with ethyl acetate and the insoluhle product (645 mg.) was filtered. The filtrate was concentrated by evapora-tion to yield 423 mg. of precipitated product. The latter filtrate was evaporated to dryness to yield 560 mg. The above three product fractions were shown to be the same when chromatographed on silica gel thin layer chromatograms using chloroform:methanol (7:3, v:v) for development and either iodine vapors or ultraviolet light for visualization of the developed plates.
Elemental analysis (percent) for C23H25N7O7S3:
Theory: C, 45.46; H, 4.15; N, 16.13 Found: C, 45.53; H, 4.47; N, 14.85.
Electrometric tritration in 66 percent DMF showed the presence of two titratable groups:
PKa 4.8 and 12.2 and an apparent molecular weight as calculated from the titration data of 587 (calculated MW=607). The infrared absorption spectrum (mineral oil mull) showing the character- -istic ~-lactam carbonyl absorption at about 2920 wave numbers and the NMR spectrum were in agreement with the expected product.
~96~7:~
UV absorption spectrum (methanol) A max 303 ~=9,246 max 275 ~=9,273 max 229 ~=16,254 Example 5 Preparation of 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-phenylacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid.
The above-named compound was ~repared by the reaction of 7-(D-a-amino-a-phenylacetamido)-3-acetoxymethyl-3-cephem-4-carboxylic acid (cephaloglycine) with N-methyl-aminocarbonyl-N-methylcarbamoyl chloride by following the reaction conditions employed in Example 3. The product (158 mg.) was obtained as a white crystalline solid.
Nuclear magnetic resonance spectrum (60 MHz., DMSO
d6): 7.45 (s, 5H), 5.9-5.4 (m, 2H), 5.2-4.4 tm, 3H) 3.5 ~broad, 2H), 3.15 (s, 3H), 2.7 (s, 3H) and 2.05 (s, 3H) delta.
Example 6 Preparation of 7-[D-a-(imidazolidine-2-one-1-ylcarbonyl-amino)-~-phenylacetamido]-3-acetoxymethyl-3-cephem-4-carboxy-lic ncid.
A suspension of 17.66 g. of cephaloglycine di-hydrate in 150 ml. of tetrahydrofuran-water (80 percent THF) was cooled in an ice bath and the pH of the suspension was adjusted to 7.8-8.2 by the addition of triethylamine. To the cold (0C.) suspension was added in small portions 5.94 g. of N-chlorocarbonylimidazolidine-2-one. Throughout the addition of the acid chloride, the pH of the reaction mixture was maintained between 7.5 and 8n 0 by adding triethylamine as required. Following the addition of the acid chloride, the reaction mixture was stirred at 0C. for 30 minutes and then at room temperature for another 20 minutes. The reaction mixture (pH 7.5) was diluted with 130 ml. of water and then evaporated to remove most of the THF. The aqueous phase was extracted once with ether and was then layered with ethyl acetate. The pH of the aqueous layer was adjusted to 1.5 to 2.0 with dilute hydrochloric acid. The ethyl acetate layer was separated and was washed with water and dried over magnesi~m sulfate. Evaporation of the dried ethyl acetate solution under reduced pressure provided the product as an amorphous solid.
Example 7 By following the acylation procedures and condi-tions described by Example 6, 7-(D--amino-a-phenylacetamido)-3-(1-methyl-lH-tetrazole-5~ylthiomethyl)-3-cephem-4-carboxy-lic acid is reacted with N-chlorocarbonylimidazolidine-2-one to provide 7-[D-(a-(imidazolidine-2-one-1-ylcarbonylamino)-a-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
Example 8 By following the procedures and by employing the solvents and conditions described in the acylation of Example
6, 7-(D-a-amino-a-phenylacetamido)-3-(5-methyl-1,3,4-thia-diazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid is reacted with chlorocarbonylimidazolidine-2-one to provide 7-[D-a-37~
(imidazolidine-2-one-1-ylcarbonylamino)-a-phenylaceta~ido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-car-boxylic acid.
Example ~
Preparation of Sodium 7-[-(3-methylcarbamoyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylate.
To a suspension of 2.88 g. (6 mmole) of sodium
(imidazolidine-2-one-1-ylcarbonylamino)-a-phenylaceta~ido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-car-boxylic acid.
Example ~
Preparation of Sodium 7-[-(3-methylcarbamoyl-1-ureido)-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylate.
To a suspension of 2.88 g. (6 mmole) of sodium
7-[D-a-amino-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylate in 48 ml.
of dry acetontrile at room temperature were added 6 ml. of BSA. When an homogeneous solution was obtained 5.2 g. of p-nitrophenyl methylcarbamoylcarbamate were added. The reaction mixture was stirred for one hour and was poured into a mixture of water and ethyl acetate. The pH was adjusted to 6 and the ethyl acetate phase was separated and replaced with fresh ethyl acetate. The pH of the aqueous phase was adjusted to pH 2.5. The aqueous layer was separ-ated and discarded. The ethyl acetate phase was washed with dilute hydrochloric acid (pH 2.0) and fresh water was added. The pH was finally adjusted to 5.5 and the aqueous phase lyophilized to yield 1.3 g. of the product as a light yellow powder.
NMR(DMSO-d6): 2.7 (s, 6H, NHCH3 & thiadiazole CH3), 3.5 (broad, 2H, C2-H2), 5O0 (d, J=5, lH, C6-H), 5.4-5.9 (m, 2H, C7-H & side chain CH), 6.9 (d, J=9, 2H, aromatic) and 7.4 (d, J=9, 2H, aromatic) delta.
~9~i3,7;~
Example 10 Preparation of Sodium 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-~-phenylacetamido]-3-(5-methyl-1,3,4-thiadiazole-2-y]thiomethyl)-3-cephem-4-carboxylate.
To a suspension of 2.78 g. of sodium 7-(D-a-amino-a-phenylacetamido)-3-(5-methyl-1,3,4-thiadiazole-2-ylthio-methyl)-3-cephem-4-carboxylate in 48 ml of dry acetonitrile containing 12 ml. of propylene oxide were added 6 ml. of bis-(trimethylsilyl)acetamide. When a homogeneous solution was obtained the solution was cooled to about 0C. and a solution of 6 mmoles of N-methylaminocarbonyl-N-methyl-carbamoyl chloride in 12 ml. of dry acetonitrile was added.
The reaction mixture was stirred for 2 hours.
The product was recovered by following the work-up procedures described in Example 9 to yield 1.1 g. of the sodium salt.
IR (mull): ~-lactam carbonyl absorption at about 2920 cm 1 NMR (DMSO d6): 2.7 (Broad, 6H, NHCH3 & Thiadiazole CH3), 3.1 (s, 3H, N-CH3), 4.4 (Broad, 2H, C(3')H2), 4.9 (d, J=4.5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)H & Side Chain CH), 9.4 (d, J=9, lH, NH) and 10.0 (d, J=7, lH, NH) delta.
Example 11 Preparation of 7-la-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl)-3-cephem-4-carboxylic acid.
To a suspension of 234 mg. of 7-[a-amino-a-(2-thienyl) acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio i373 methyl)-3-cephem-4-carboxylic acid in 4 ml. of dry aceton-itrile containing 1 ml. of propylene oxide was added under argon 0.5 ml. of BSA to form a homogeneous solution. The solution was cooled to 0C. and a solution of 75 mg. of N-methylaminocarbonyl-N-methylcarbamoyl chloride in 1 ml. of acetonitrile. The reaction mixture was stirred for 2 hours and was then poured into a mixture of water-ethyl acetate.
The pH of the aqueous phase was adjusted to pH 6 and the organic phase separated. Fresh ethyl acetate was added to the aqueous phase and the pH adjusted to 2.5 with dilute hydrochloric acid. The organic phase was separated, dried and evaporated to dryness to yield the product.
Elemental analysis for: C20H23NgO6S3 Theory: C, 41.30; H, 3.99; N, 21.68 Found: C, 41.78; H, 4.14; N, 21.73.
UV(methanol): ~ max 238 ~ 17,475 max 270 ~ 9,000 Example 12 Preparation of p-nitrophenyl methylcarbamoylcarbamate.
Methylurea (3.7 g., S0 mmole) and p-nitrophenyl chloroformate (50 mmole) were allowed to react under nitro-gen in 10 ml. of dry THF. The reaction mixture became clear initially and the product began to precipitate from the clear solution. The mixture was stirred for about 18 hours and the precipitated product was filtered. The product was washed with water and diethyl ether to yield 5.9 g. of approximately a 50:50 mixture of p-nitrophenyl methylcar-bamoylcarbamate and p-nitrophenyl carbamoyl-N-methylcarbamate as shown by NMR.
~39~3~3 Example 13 Preparation of 7-[~-(3-methylcarbamoyl-1-ureido)-phenyl-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
A suspension under argon of 2 mmoles of 7-(a-amino-a-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 16 ml. of dry acetonitrile was solubilized by adding 2 ml of BSA. With stirring, 4 mmoles of the product mixture obtained as described by Example 12 (mixture of p-nitrophenyl methylcarbamoylcarbamate and p-nitrophenyl carbamoyl-N-methylcarbamate) were added. The reaction mixture became clear in a few minutes and was stirred for about 2 hours.
The reaction mixture was poured into a mixture of water-ethyl acetate and the pH adjusted to 6. The ethyl acetate layer was separated and discarded. The aqueous phase was relayered with fresh ethyl acetate and the pH of the aqueous phase was the adjusted to pH 2.5. The organic layer was separated, washed with water, dried and evaporated in vacuo. The product residue was triturated with diethyl ether to yield 600 mg. of product as a faintly yellow powder.
Elemental analysis for: C21H23NgO6S2 Theory: C, 44.91; H, 4.13; 22.45; S, 11.42 Found: C, 44.66; H, 4.34; 22.29; S, 11.28.
UV(methanol): ~ max 272 11 , 091 NMR (DMSO d6): 2.6 (d, J5H2, 3H, NHCH3), 3.9 (S, 3H), -CH3 on tetrazole), 3.55 (Broad, 2H, CH2), 5.0 (d, J=5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)H & Side ~91 i:373 Chain CH), 7.3 (S, 5H, Q), 8.4 (d, J-7, lH, NH),
of dry acetontrile at room temperature were added 6 ml. of BSA. When an homogeneous solution was obtained 5.2 g. of p-nitrophenyl methylcarbamoylcarbamate were added. The reaction mixture was stirred for one hour and was poured into a mixture of water and ethyl acetate. The pH was adjusted to 6 and the ethyl acetate phase was separated and replaced with fresh ethyl acetate. The pH of the aqueous phase was adjusted to pH 2.5. The aqueous layer was separ-ated and discarded. The ethyl acetate phase was washed with dilute hydrochloric acid (pH 2.0) and fresh water was added. The pH was finally adjusted to 5.5 and the aqueous phase lyophilized to yield 1.3 g. of the product as a light yellow powder.
NMR(DMSO-d6): 2.7 (s, 6H, NHCH3 & thiadiazole CH3), 3.5 (broad, 2H, C2-H2), 5O0 (d, J=5, lH, C6-H), 5.4-5.9 (m, 2H, C7-H & side chain CH), 6.9 (d, J=9, 2H, aromatic) and 7.4 (d, J=9, 2H, aromatic) delta.
~9~i3,7;~
Example 10 Preparation of Sodium 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-~-phenylacetamido]-3-(5-methyl-1,3,4-thiadiazole-2-y]thiomethyl)-3-cephem-4-carboxylate.
To a suspension of 2.78 g. of sodium 7-(D-a-amino-a-phenylacetamido)-3-(5-methyl-1,3,4-thiadiazole-2-ylthio-methyl)-3-cephem-4-carboxylate in 48 ml of dry acetonitrile containing 12 ml. of propylene oxide were added 6 ml. of bis-(trimethylsilyl)acetamide. When a homogeneous solution was obtained the solution was cooled to about 0C. and a solution of 6 mmoles of N-methylaminocarbonyl-N-methyl-carbamoyl chloride in 12 ml. of dry acetonitrile was added.
The reaction mixture was stirred for 2 hours.
The product was recovered by following the work-up procedures described in Example 9 to yield 1.1 g. of the sodium salt.
IR (mull): ~-lactam carbonyl absorption at about 2920 cm 1 NMR (DMSO d6): 2.7 (Broad, 6H, NHCH3 & Thiadiazole CH3), 3.1 (s, 3H, N-CH3), 4.4 (Broad, 2H, C(3')H2), 4.9 (d, J=4.5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)H & Side Chain CH), 9.4 (d, J=9, lH, NH) and 10.0 (d, J=7, lH, NH) delta.
Example 11 Preparation of 7-la-(3-methylcarbamoyl-3-methyl-1-ureido)-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio-methyl)-3-cephem-4-carboxylic acid.
To a suspension of 234 mg. of 7-[a-amino-a-(2-thienyl) acetamido]-3-(1-methyl-lH-tetrazole-5-ylthio i373 methyl)-3-cephem-4-carboxylic acid in 4 ml. of dry aceton-itrile containing 1 ml. of propylene oxide was added under argon 0.5 ml. of BSA to form a homogeneous solution. The solution was cooled to 0C. and a solution of 75 mg. of N-methylaminocarbonyl-N-methylcarbamoyl chloride in 1 ml. of acetonitrile. The reaction mixture was stirred for 2 hours and was then poured into a mixture of water-ethyl acetate.
The pH of the aqueous phase was adjusted to pH 6 and the organic phase separated. Fresh ethyl acetate was added to the aqueous phase and the pH adjusted to 2.5 with dilute hydrochloric acid. The organic phase was separated, dried and evaporated to dryness to yield the product.
Elemental analysis for: C20H23NgO6S3 Theory: C, 41.30; H, 3.99; N, 21.68 Found: C, 41.78; H, 4.14; N, 21.73.
UV(methanol): ~ max 238 ~ 17,475 max 270 ~ 9,000 Example 12 Preparation of p-nitrophenyl methylcarbamoylcarbamate.
Methylurea (3.7 g., S0 mmole) and p-nitrophenyl chloroformate (50 mmole) were allowed to react under nitro-gen in 10 ml. of dry THF. The reaction mixture became clear initially and the product began to precipitate from the clear solution. The mixture was stirred for about 18 hours and the precipitated product was filtered. The product was washed with water and diethyl ether to yield 5.9 g. of approximately a 50:50 mixture of p-nitrophenyl methylcar-bamoylcarbamate and p-nitrophenyl carbamoyl-N-methylcarbamate as shown by NMR.
~39~3~3 Example 13 Preparation of 7-[~-(3-methylcarbamoyl-1-ureido)-phenyl-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
A suspension under argon of 2 mmoles of 7-(a-amino-a-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 16 ml. of dry acetonitrile was solubilized by adding 2 ml of BSA. With stirring, 4 mmoles of the product mixture obtained as described by Example 12 (mixture of p-nitrophenyl methylcarbamoylcarbamate and p-nitrophenyl carbamoyl-N-methylcarbamate) were added. The reaction mixture became clear in a few minutes and was stirred for about 2 hours.
The reaction mixture was poured into a mixture of water-ethyl acetate and the pH adjusted to 6. The ethyl acetate layer was separated and discarded. The aqueous phase was relayered with fresh ethyl acetate and the pH of the aqueous phase was the adjusted to pH 2.5. The organic layer was separated, washed with water, dried and evaporated in vacuo. The product residue was triturated with diethyl ether to yield 600 mg. of product as a faintly yellow powder.
Elemental analysis for: C21H23NgO6S2 Theory: C, 44.91; H, 4.13; 22.45; S, 11.42 Found: C, 44.66; H, 4.34; 22.29; S, 11.28.
UV(methanol): ~ max 272 11 , 091 NMR (DMSO d6): 2.6 (d, J5H2, 3H, NHCH3), 3.9 (S, 3H), -CH3 on tetrazole), 3.55 (Broad, 2H, CH2), 5.0 (d, J=5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)H & Side ~91 i:373 Chain CH), 7.3 (S, 5H, Q), 8.4 (d, J-7, lH, NH),
8.8 (S, lH, NH) and 9.4 (d, J=9, lH, NH) delta.
Example 14 Preparation of 7-~a-(3-methylcarbamoyl-1-ureido)-a-(4-hydro-xyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a suspension of 988 mg. (2 mmole) of 7-[a-amino-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thia-diazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid in 16 ml.
of dry acetonitrile were added 2 ml. of BSA under argon. An homogeneous solution was obtained and 1.43 g. (6 mmole) of the product mixture containing 50% of p-nitrophenyl methyl-carbamoylcarbamate (Example 12) were added. After stirring for one hour the product was recovered from the reaction mixture by following the work-up procedures described in Example 13. The product, 524 mg., was obtained as a light i yellow powder.
UV(methanol): A max 232 ~ 16,072 ~ max 275 ~ 14,309 IRtmull): ~-lactam carbonyl absorption at about 2900 cm 1 Example 15 Preparation of 7-[a-(3-methylcarbamoyl-1-ureido)-a-(2-thienyl) acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a suspension of 435 mg. (0.93 mmole) of 7-[D-a-amino-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-yl-, ~ ~
~9637~
thiomethyl)-3-cephem-4-carboxylic acid in 8 ml. of dry acetonitrile was added 1 ml. of b:is-(trimethylsilyl)acetamide.
After an homogeneous solution was obtained 1.4 g. of p-nitro-phenyl methylcarbamoylcarbamate were added.
The reaction mixture was stirred at room tempera-ture for 90 minutes. The product was recovered from the reaction mixture by following the work-up procedures describ-ed in Examp]e 11. The product was obtained as a white powder weighing 341 mg.
Elemental analysis for: C29H21NgO6S3:
Theory: C, 40.20; H, 3.73; N, 22.21; S, 16.95 Found: C, 39.86; H, 4.02; N, 22.88; S, 14.66.
I.R.(mull) ~-lactam carbonyl absorption at about 2920 cm 1.
U.V.(methanol): ~ max 235 ~ 15,459 ~ max 272 ~ 9,360 NMR(DMSO d6): 2.6(d, J=4.5, 3H, NHCH3), 3.6 (Broad, 2H, C(2)H2), 3.9 (5, 3H, tetrazole CH3), 4.25 (Broad, 2H, C(3')H2), 5.1 (d, J=5, lH, C(6)H), 5.6-5.9(m, 2H, C(7)H & Side Chain CH), 6.9-7.6(m, 4H, Thiophene & lNH), 8.4 (d, J=8, lH, NH), 8.9 (S, lH, NH) and 9.5 (d, J=8.5, lH, NH) delta.
Example 16 Preparation of p-nitrophenyl phenylcarbamoylcarbamate.
To a stirred solution of 6.8 g. of phenylurea in 50 ml. of dry THF maintained at 0C. under nitrogen were ~96373 added 5.05 g. of p-nitrophenyl chloroformate. The reaction mixture was allowed to warm to room temperature and was stirred for about 18 hours. The mixture was evaporated to dryness and the residue dissolved in ethyl acetate. The solution was washed twice with water, twice with brine, and was filtered through sodium sulfate. The filtrate was evapor-ated to dryness to yield 4.9 g. of the product as a white product.
Example 17 Preparation of 7-[~-(3-phenylcarbamoyl-1-ureido)-a-phenyl-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
A suspension of 950 mg. (2 mmole) of 7-(D-a-amino-a-phenylacetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 16 ml. of dry acetonitrile at 0C. was solubilized under nitrogen with 2 ml. of BSA. With stirring 1.2 g. of p-nitrophenyl N-phenylcarbamoylcarbamate, prepared as described in Example 16, were added to the solution. The reaction mixture was stirred for one hour and the product recovered by following the work-up procedures described in Example 11. The product was obtained as a light yellow powder weighing 839 mg.
NMR(DMSO d6): 3.6 (Broad, 2H C(2)-H2), 3.95 (S, 3H, Tetrazole-CH3), 4.3 (Broad, 2H, C(3')-H2), 5.0 (d, J=5, lH, C(6)-H), 5.5-5.9 (m, 2H, C(7)-H & Side Chain CH), 7.0-7.6 (Broad, lOH, Aromatic), 8.4 (d, J=7.5, lH, NH), 9.1 (s, lH, NH), 9.6 (d, J=9, lH, NH), 9.8 (S, lH, NH).
1~6373 Example 18 Preparation of 7-[a-(3-benzylcarbamoyl-1-ureido)-a-phenyl-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
By following the procedure described in Example 17, 2 mmoles of 7-(a-amino-a-phenylace~amido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid were dissolved in acetonitrile with BSA and reacted with 1.26 g.
of p-nitrophenyl N-benzylcarbamoylcarbamate to yield the title compound.
NMR(DMSO d6): 3.6(Broad, 2H, C(3)H2), 3.9(S, 3H, Tetrazole CH3), 4.3 (Broad, 4H, C(3')-H2 and benzyl CH2), 5.0 (d, J=5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)H & Side Chain CH), 7.2-7.6 tm, lOH, Aromatic), 7.8 (t, J=5.5, lH), 8.4 (d, J=7, lH, NH), 8.95 (S, lH, NH), 9.5 (d, J=8, lH, NH).
Example 19 Preparation of 7-[a-(3-furfurylcarbamoyl-1-ureido)-a-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
By following the procedure described in Example 17, 2 mmoles of 7-(a-amino-~-phenylacetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid were reacted at 0C. in dry acetonitrii~ with BSA and 1.22 g. of p-nitrophenyl N-furfurylcarbamoylcarbamate to obtain the title compound.
1~96~3~3 NMR(DMSO d6): 3.55 (Broad, 2H, C(2)-H2), 3.9 (S, 3H, Tetrazole CH3), 4.3 (Bxoad, 4H, C(3')H2 & Thiophene CH2), 5.0 (d, J=5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)-H & Side Chain CH), 6.3 (m, 2H, thiophene aromatic), 7.2-7.9 (m, 7H, aromatic & NH), 8.4 (d, J=7, lH, NH), 8.9 (s, lH, NH), 9.4 (d, J=8, lH, NH).
Example 20 Preparation of p-nitrophenyl carbamoylcarbamate.
To a mixture of 1.20 g. (20 mmole) of urea and 2.02 g. (10 mmole) of p-nitrophenyl chloroformate in a dry flask under nitrogen were added 10 ml. of dry acetonitrile.
The reaction mixture momentarily became clear and then a precipitate formed. The mixture was tirred for 18 hours at room temperature and the precipitate was filtered, washed with water and dried under vacuum. The dried prcduct was triturated with ether and redried to yield 1.0 g. of crystal-line product.
Example 21 Preparation of 7-[a-(3-carbamoyl-1-ureido)-~-phenylacetamido~-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxy-lic acid.
To a suspension of 2 mmole of 7-(a-amino-~-phenyl-acetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 20 ml. of dry acetonitrile under argon were added 3/4 ml. of BSA. When an homogeneous solu-tion was obtained it was evaporated to dryness. The residual dry off-white powder was dissolved in DMF and the solution ~Gi9~373 added under argon with stirring to a solution of 20 mmole of p-nitrophenyl carbamoylcarbamate (Example 20) in 10 ml. of DMF containing 20 mg. of l-hydroxybenzotriazole monohydrate.
The reaction mixture was stirred for 72 hours at room tem-perature and then was diluted with water and the product extracted with ethyl acetate at a pH of about 2.5. The extract was washed, dried and evaporated to yield the product as an amorphous powder.
Elemental analysis for: C20H2lN9o6s2 Theory: C, 43.87; H, 3.87; N, 23.02; S, 11.71 Found: C, 43.77; , 4.00; N, 22.86; S, 11.41.
UV(methanol): ~ max 250 ~ 8,957 NMR (DMS0 d6): 3.55 (Broad, 2H, C(2)H2), 3.95 (S, 3H, tetrazole-CH3), 4.45 (Broad, 2H, c(3')H2), 5.0(d, J=5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)H & Side Chain CH), 6.75 (Broad S, 2H, -NH2), 7.4 (S, 5H, phenyl), 8.51 (d, J=7, lH, NH), 8.8 (S, lH, NH~
and 9.5 (d, J=10, lH, NH) delta.
Example 22 Preparation of 3-(methylsulfonyl)imidazolidine-2-one-1-ylcarbonyl chloride.
To a suspension of 10.7 g. of imidazolidone-2 in 100 ml. of dry THF were added dropwise with stirring at room temperature 15.7 g. of methanesulfonyl chloride. The reac-tion mixture was stirred for one-hour at about 40C. and was then heated at the reflux temperature for one-hour.
The reaction mixture was evaporated in vacuo and the thick syrupy residue was dried in vacuo for about 18 1~63~;~
hours. The dried residue was crystallized from warm acetone to yield 7.1 g. of N-methylsulfonyl-imidazolidone-2. The percent elemental composition of the product was determined by microanalysis:
Calculated for: C4H8N2O3S:
Theory: C, 29.26; H, 4.91; N, 17.06; S, 19.53 Found: C, 29.47; H, 4.96; N, 17.17; S, 19.50.
A solution of 4.1 g. of the above product in dioxane was treated with 7 g. of trimethylchlorosilane and 5 g. of triethylamine.
The solution was heated at the reflux temperature for about 2.5 days and was cooled to room temperature. The precipitate of triethylamine hydrochloride was filtered and the filtrate treated with 3 ml. of phosgene. The filtrate was allowed to stand at room temperature for 2 days and was evaporated in vacuo to dryness. The residue was crystallized from warm acetone and the product further dried in vacuo to yield 2.8 g. of the title compound melting at about 178C.
Example 23 Preparation of 7-[-[3-(methylsulfonyl)imidazolidine-2-one-l-ylcarbonylamino]a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a solution of 200 mg. of 7-[~-amino-~-(2-thienyl) acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 25 ml. of dichloromethane were added 2 molar equivalents of triethylamine and a pinch of sodium sulfate. The mixture was filtered and 100 mg. of 3-1~6373 methylsulfonylimidazolidine-2-one-1-ylcarbonyl chloride were added to the filtrate. The reaction mixture was stirred for 3 hours in a water bath after which the dichloromethane was evaporated. The residue was extracted at pH 2 with ethyl acetate and the extract was washed with water and dried.
The dried extract was evaporated in vacuo and the residue recrystallized twice from acetone:diethyl ether:petroleum ether to yield 109 mg. of the product.
UV(methanolJ: ~ max 270 ~ 9,328 233 ~ 15,995 NMR(DMSO d6): 3.45 (S, 3H, CH3SO2-), 3.65 (AB, 2H, C(2)-H2), 3.8(Broad, 4H, CH2CH2), 3.95 (S, 3H, tetrazole CH3), 4.6 (AB, 2H, C(3')-H2), 5.05 (d, J=5, lH, C(6)-H), 5.75 (dd, J=8, J2=5' lH, C(7)-H), 5.88 (d, J=7.5, lH, Side Chain CH), 6.94-7.15 (m, 2H, thiophene aromatic), 7.4-7.5 ~dd, lH, thiophene aromatic), 8.72 (d, J=7, lH, NH) and 9.51 (d, J=8.5, lH, NH) delta.
Following the preparative methods described in the above examples, 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-~4-hydroxyphenyl)acetamido]-3-(1-methyl-1,2,3-triazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid and 7-[D-a-(imidazolidine-2-one-1-ylcarbonylamino)-~-phenylacetamdio]-3-(l-methyl-1,2,3-triazole-5-ylthiomethyl)-3-cephem-4-carboxy-lic acid are prepared.
Example 14 Preparation of 7-~a-(3-methylcarbamoyl-1-ureido)-a-(4-hydro-xyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a suspension of 988 mg. (2 mmole) of 7-[a-amino-a-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thia-diazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid in 16 ml.
of dry acetonitrile were added 2 ml. of BSA under argon. An homogeneous solution was obtained and 1.43 g. (6 mmole) of the product mixture containing 50% of p-nitrophenyl methyl-carbamoylcarbamate (Example 12) were added. After stirring for one hour the product was recovered from the reaction mixture by following the work-up procedures described in Example 13. The product, 524 mg., was obtained as a light i yellow powder.
UV(methanol): A max 232 ~ 16,072 ~ max 275 ~ 14,309 IRtmull): ~-lactam carbonyl absorption at about 2900 cm 1 Example 15 Preparation of 7-[a-(3-methylcarbamoyl-1-ureido)-a-(2-thienyl) acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a suspension of 435 mg. (0.93 mmole) of 7-[D-a-amino-a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-yl-, ~ ~
~9637~
thiomethyl)-3-cephem-4-carboxylic acid in 8 ml. of dry acetonitrile was added 1 ml. of b:is-(trimethylsilyl)acetamide.
After an homogeneous solution was obtained 1.4 g. of p-nitro-phenyl methylcarbamoylcarbamate were added.
The reaction mixture was stirred at room tempera-ture for 90 minutes. The product was recovered from the reaction mixture by following the work-up procedures describ-ed in Examp]e 11. The product was obtained as a white powder weighing 341 mg.
Elemental analysis for: C29H21NgO6S3:
Theory: C, 40.20; H, 3.73; N, 22.21; S, 16.95 Found: C, 39.86; H, 4.02; N, 22.88; S, 14.66.
I.R.(mull) ~-lactam carbonyl absorption at about 2920 cm 1.
U.V.(methanol): ~ max 235 ~ 15,459 ~ max 272 ~ 9,360 NMR(DMSO d6): 2.6(d, J=4.5, 3H, NHCH3), 3.6 (Broad, 2H, C(2)H2), 3.9 (5, 3H, tetrazole CH3), 4.25 (Broad, 2H, C(3')H2), 5.1 (d, J=5, lH, C(6)H), 5.6-5.9(m, 2H, C(7)H & Side Chain CH), 6.9-7.6(m, 4H, Thiophene & lNH), 8.4 (d, J=8, lH, NH), 8.9 (S, lH, NH) and 9.5 (d, J=8.5, lH, NH) delta.
Example 16 Preparation of p-nitrophenyl phenylcarbamoylcarbamate.
To a stirred solution of 6.8 g. of phenylurea in 50 ml. of dry THF maintained at 0C. under nitrogen were ~96373 added 5.05 g. of p-nitrophenyl chloroformate. The reaction mixture was allowed to warm to room temperature and was stirred for about 18 hours. The mixture was evaporated to dryness and the residue dissolved in ethyl acetate. The solution was washed twice with water, twice with brine, and was filtered through sodium sulfate. The filtrate was evapor-ated to dryness to yield 4.9 g. of the product as a white product.
Example 17 Preparation of 7-[~-(3-phenylcarbamoyl-1-ureido)-a-phenyl-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
A suspension of 950 mg. (2 mmole) of 7-(D-a-amino-a-phenylacetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 16 ml. of dry acetonitrile at 0C. was solubilized under nitrogen with 2 ml. of BSA. With stirring 1.2 g. of p-nitrophenyl N-phenylcarbamoylcarbamate, prepared as described in Example 16, were added to the solution. The reaction mixture was stirred for one hour and the product recovered by following the work-up procedures described in Example 11. The product was obtained as a light yellow powder weighing 839 mg.
NMR(DMSO d6): 3.6 (Broad, 2H C(2)-H2), 3.95 (S, 3H, Tetrazole-CH3), 4.3 (Broad, 2H, C(3')-H2), 5.0 (d, J=5, lH, C(6)-H), 5.5-5.9 (m, 2H, C(7)-H & Side Chain CH), 7.0-7.6 (Broad, lOH, Aromatic), 8.4 (d, J=7.5, lH, NH), 9.1 (s, lH, NH), 9.6 (d, J=9, lH, NH), 9.8 (S, lH, NH).
1~6373 Example 18 Preparation of 7-[a-(3-benzylcarbamoyl-1-ureido)-a-phenyl-acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
By following the procedure described in Example 17, 2 mmoles of 7-(a-amino-a-phenylace~amido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid were dissolved in acetonitrile with BSA and reacted with 1.26 g.
of p-nitrophenyl N-benzylcarbamoylcarbamate to yield the title compound.
NMR(DMSO d6): 3.6(Broad, 2H, C(3)H2), 3.9(S, 3H, Tetrazole CH3), 4.3 (Broad, 4H, C(3')-H2 and benzyl CH2), 5.0 (d, J=5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)H & Side Chain CH), 7.2-7.6 tm, lOH, Aromatic), 7.8 (t, J=5.5, lH), 8.4 (d, J=7, lH, NH), 8.95 (S, lH, NH), 9.5 (d, J=8, lH, NH).
Example 19 Preparation of 7-[a-(3-furfurylcarbamoyl-1-ureido)-a-phenylacetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
By following the procedure described in Example 17, 2 mmoles of 7-(a-amino-~-phenylacetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid were reacted at 0C. in dry acetonitrii~ with BSA and 1.22 g. of p-nitrophenyl N-furfurylcarbamoylcarbamate to obtain the title compound.
1~96~3~3 NMR(DMSO d6): 3.55 (Broad, 2H, C(2)-H2), 3.9 (S, 3H, Tetrazole CH3), 4.3 (Bxoad, 4H, C(3')H2 & Thiophene CH2), 5.0 (d, J=5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)-H & Side Chain CH), 6.3 (m, 2H, thiophene aromatic), 7.2-7.9 (m, 7H, aromatic & NH), 8.4 (d, J=7, lH, NH), 8.9 (s, lH, NH), 9.4 (d, J=8, lH, NH).
Example 20 Preparation of p-nitrophenyl carbamoylcarbamate.
To a mixture of 1.20 g. (20 mmole) of urea and 2.02 g. (10 mmole) of p-nitrophenyl chloroformate in a dry flask under nitrogen were added 10 ml. of dry acetonitrile.
The reaction mixture momentarily became clear and then a precipitate formed. The mixture was tirred for 18 hours at room temperature and the precipitate was filtered, washed with water and dried under vacuum. The dried prcduct was triturated with ether and redried to yield 1.0 g. of crystal-line product.
Example 21 Preparation of 7-[a-(3-carbamoyl-1-ureido)-~-phenylacetamido~-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxy-lic acid.
To a suspension of 2 mmole of 7-(a-amino-~-phenyl-acetamido)-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 20 ml. of dry acetonitrile under argon were added 3/4 ml. of BSA. When an homogeneous solu-tion was obtained it was evaporated to dryness. The residual dry off-white powder was dissolved in DMF and the solution ~Gi9~373 added under argon with stirring to a solution of 20 mmole of p-nitrophenyl carbamoylcarbamate (Example 20) in 10 ml. of DMF containing 20 mg. of l-hydroxybenzotriazole monohydrate.
The reaction mixture was stirred for 72 hours at room tem-perature and then was diluted with water and the product extracted with ethyl acetate at a pH of about 2.5. The extract was washed, dried and evaporated to yield the product as an amorphous powder.
Elemental analysis for: C20H2lN9o6s2 Theory: C, 43.87; H, 3.87; N, 23.02; S, 11.71 Found: C, 43.77; , 4.00; N, 22.86; S, 11.41.
UV(methanol): ~ max 250 ~ 8,957 NMR (DMS0 d6): 3.55 (Broad, 2H, C(2)H2), 3.95 (S, 3H, tetrazole-CH3), 4.45 (Broad, 2H, c(3')H2), 5.0(d, J=5, lH, C(6)H), 5.4-5.9 (m, 2H, C(7)H & Side Chain CH), 6.75 (Broad S, 2H, -NH2), 7.4 (S, 5H, phenyl), 8.51 (d, J=7, lH, NH), 8.8 (S, lH, NH~
and 9.5 (d, J=10, lH, NH) delta.
Example 22 Preparation of 3-(methylsulfonyl)imidazolidine-2-one-1-ylcarbonyl chloride.
To a suspension of 10.7 g. of imidazolidone-2 in 100 ml. of dry THF were added dropwise with stirring at room temperature 15.7 g. of methanesulfonyl chloride. The reac-tion mixture was stirred for one-hour at about 40C. and was then heated at the reflux temperature for one-hour.
The reaction mixture was evaporated in vacuo and the thick syrupy residue was dried in vacuo for about 18 1~63~;~
hours. The dried residue was crystallized from warm acetone to yield 7.1 g. of N-methylsulfonyl-imidazolidone-2. The percent elemental composition of the product was determined by microanalysis:
Calculated for: C4H8N2O3S:
Theory: C, 29.26; H, 4.91; N, 17.06; S, 19.53 Found: C, 29.47; H, 4.96; N, 17.17; S, 19.50.
A solution of 4.1 g. of the above product in dioxane was treated with 7 g. of trimethylchlorosilane and 5 g. of triethylamine.
The solution was heated at the reflux temperature for about 2.5 days and was cooled to room temperature. The precipitate of triethylamine hydrochloride was filtered and the filtrate treated with 3 ml. of phosgene. The filtrate was allowed to stand at room temperature for 2 days and was evaporated in vacuo to dryness. The residue was crystallized from warm acetone and the product further dried in vacuo to yield 2.8 g. of the title compound melting at about 178C.
Example 23 Preparation of 7-[-[3-(methylsulfonyl)imidazolidine-2-one-l-ylcarbonylamino]a-(2-thienyl)acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid.
To a solution of 200 mg. of 7-[~-amino-~-(2-thienyl) acetamido]-3-(1-methyl-lH-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 25 ml. of dichloromethane were added 2 molar equivalents of triethylamine and a pinch of sodium sulfate. The mixture was filtered and 100 mg. of 3-1~6373 methylsulfonylimidazolidine-2-one-1-ylcarbonyl chloride were added to the filtrate. The reaction mixture was stirred for 3 hours in a water bath after which the dichloromethane was evaporated. The residue was extracted at pH 2 with ethyl acetate and the extract was washed with water and dried.
The dried extract was evaporated in vacuo and the residue recrystallized twice from acetone:diethyl ether:petroleum ether to yield 109 mg. of the product.
UV(methanolJ: ~ max 270 ~ 9,328 233 ~ 15,995 NMR(DMSO d6): 3.45 (S, 3H, CH3SO2-), 3.65 (AB, 2H, C(2)-H2), 3.8(Broad, 4H, CH2CH2), 3.95 (S, 3H, tetrazole CH3), 4.6 (AB, 2H, C(3')-H2), 5.05 (d, J=5, lH, C(6)-H), 5.75 (dd, J=8, J2=5' lH, C(7)-H), 5.88 (d, J=7.5, lH, Side Chain CH), 6.94-7.15 (m, 2H, thiophene aromatic), 7.4-7.5 ~dd, lH, thiophene aromatic), 8.72 (d, J=7, lH, NH) and 9.51 (d, J=8.5, lH, NH) delta.
Following the preparative methods described in the above examples, 7-[a-(3-methylcarbamoyl-3-methyl-1-ureido)-a-~4-hydroxyphenyl)acetamido]-3-(1-methyl-1,2,3-triazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid and 7-[D-a-(imidazolidine-2-one-1-ylcarbonylamino)-~-phenylacetamdio]-3-(l-methyl-1,2,3-triazole-5-ylthiomethyl)-3-cephem-4-carboxy-lic acid are prepared.
Claims (42)
1. A process for preparing ureido substituted cephalosporin compounds of the formula I
wherein R is a 3-substituted ureido group represented by the formula wherein R" is hydrogen, C1-C3 alkyl, allyl, propargyl, C3-C6 cycloalkyl, phenyl, benzyl, or furfuryl; and R' is hydrogen or methyl;
or R is a cyclic ureido group of the formula wherein Y is hydrogen, acetyl or methanesulfonyl, and n is 2 or 3;
R1 is phenyl, hydroxyphenyl, halophenyl, hydroxy substituted halophenyl, or ;
R2 is acetoxy, , or wherein Z is C1-C4 lower alkyl;
R3 is hydrogen, indanyl, phthalidyl, or an acyloxymethyl group of the formula wherein Y' is C1-C4 alkyl or phenyl; and when R3 is hydrogen, the pharmaceutically acceptable non-toxic salts thereof; characterized by reacting a compound of the formula II
II
wherein R1 and R2 are as defined above, with a compound of the formula wherein R is as defined above and A is -C1 or ;
and if desired converting the acid so obtained wherein R3 is hydrogen to the corresponding ester wherein R3 is other than hydrogen ; and where desired, when R3 is hydrogen, forming a pharmaceutically acceptable, non-toxic salt of said compound of formula I.
wherein R is a 3-substituted ureido group represented by the formula wherein R" is hydrogen, C1-C3 alkyl, allyl, propargyl, C3-C6 cycloalkyl, phenyl, benzyl, or furfuryl; and R' is hydrogen or methyl;
or R is a cyclic ureido group of the formula wherein Y is hydrogen, acetyl or methanesulfonyl, and n is 2 or 3;
R1 is phenyl, hydroxyphenyl, halophenyl, hydroxy substituted halophenyl, or ;
R2 is acetoxy, , or wherein Z is C1-C4 lower alkyl;
R3 is hydrogen, indanyl, phthalidyl, or an acyloxymethyl group of the formula wherein Y' is C1-C4 alkyl or phenyl; and when R3 is hydrogen, the pharmaceutically acceptable non-toxic salts thereof; characterized by reacting a compound of the formula II
II
wherein R1 and R2 are as defined above, with a compound of the formula wherein R is as defined above and A is -C1 or ;
and if desired converting the acid so obtained wherein R3 is hydrogen to the corresponding ester wherein R3 is other than hydrogen ; and where desired, when R3 is hydrogen, forming a pharmaceutically acceptable, non-toxic salt of said compound of formula I.
2. Compounds of the formula I wherein R, R1, R2 and R3 are as defined in claim 1,when prepared by the process of claim 1 or by an obvious chemical equivalent thereof.
3, The process for preparing 7-[.alpha.-(3-methylcarbamoyl-3-methyl-1-ureido)-.alpha.-(4-hydroxyphenyl) acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-(4-hydroxyphenyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid with N-methylamino-carbonyl-N-methylcarbamoyl chloride.
4. 7-¦.alpha.-(3-Methylcarbamoyl-3-methyl-1-ureido)-.alpha.-(4-hydroxyphenyl)acetamido]-3-(1-methyl-1H-tetrazole-5-yl-thiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 3 or by an obvious chemical equivalent thereof.
The process for preparing 7- [.alpha.-(3-methylcarbamoyl-3-methyl-1-ureido)-.alpha.-phenylacetamido]-3-(5-methyl-1,3,4-thia-diazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-a-amino-.alpha.-phenylacetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid with N-methylaminocarbonyl-N-methylcarbamoyl chloride.
6. 7-[.alpha.-13-Methylcarbamoyl-3-methyl-1-ureido)-.alpha.-phenylacetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 5 or by an obvious chemical equivalent thereof.
7 The process for preparing 7-[.alpha.-(3-methylcarbamoyl-3-methyl-1-ureido)-.alpha.-(4-hydroxyphenyl)-acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-(4-hydroxyphenyl)-acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid with N-methylaminocarbonyl-N
methylcarbamoyl chloride.
methylcarbamoyl chloride.
8. 7-[.alpha.-(3-Methylcarbamoyl-3-methyl-1-ureido)-.alpha.-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 7 or by an obvious chemical equivalent thereof.
9. The process for preparing 7-[.alpha.-(3-methyl-carbamoyl-3-methyl-1-ureido)-.alpha.-(2-thienyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-(2-thienyl-acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid with N-methylaminocarbonyl-N-methylcarbamoyl chloride
10. 7-[.alpha.-(3-Methylcarbamoyl-3-methyl-1-ureido)-.alpha.-(2-thienyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthio-methyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 9 or by an obvious chemical equivalent thereof.
11. The process for preparing 7-[.alpha.-3-methyl-carbamoyl-1-ureido)-.alpha.-phenylacetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-phenylacetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid with p-nitrophenyl N-methylcarbamoylcarbamate.
12. 7-[.alpha.-(3-Methylcarbamoyl-1-ureido)-.alpha.-phenyl-acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 11 or by an obvious chemical equivalent thereof.
13. The process for preparing 7-[.alpha.-3-methyl-carbamoyl-1-ureido)-.alpha.-(2-thienyl)acetamiao]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-(2-thienyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-car-boxylic acid with p-nitrophenyl N-methylcarbamoylcarbamate.
14. 7-[.alpha.-(3-Methylcarbamoyl-1-ureido)-.alpha.-(2-thienyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid,when prepared by the process of claim 13 or by an obvious chemical equivalent thereof.
The process for preparing 7-[.alpha.-(3-methyl-carbamoyl-1-ureido)-.alpha.-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid with p-nitrophenyl N-methylcarbamoylcarbamate.
16. 7-[.alpha.-(3-Methylcarbamoyl-1-ureido)-.alpha.-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4,-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 15 or by an obvious chemical equivalent thereof.
17. The process for preparing 7-[.alpha.-(3-phenylcar-bamoyl -1-ureido)-.alpha.-phenylacetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-phenylacetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-car-boxylic acid with p-nitrophenyl N-phenylcarbamoyl-carbamate.
18. 7-[.alpha.-(3-phenylcarbamoyl-1-ureido)- .alpha.-phenyl-acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylie acid, when prepared by the process of claim 17 or by an obvious chemical equivalent thereof.
19. The process for preparing 7-[.alpha.-(3-benzylcarbamoyl-1-ureido)-.alpha.-phenylacetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-(.alpha.-amino-.alpha.-phenylacetamido)-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid with p-nitrophenyl N-benzylcarbamoyl carbamate.
20. 7-[.alpha.-(3-benzylcarbamoyl-1-ureido)-.alpha.-phenyl-acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 19 or by an obvious chemical equivalent thereof.
21. The process for preparing 7-[.alpha.-(3-furfurylcarbamoyl-1-ureido)-.alpha.-phenylacetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid, which comprises reacting 7-(.alpha.-amino-.alpha.-phenylacetamido)-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid with p-nitrophenyl N-furfurylcarbamoyl carbamate.
22. 7-[.alpha.-(3-furfurylcarbamoyl-1-ureido)-.alpha.-phenyl-acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 21 or by an obvious chemical equivalent thereof.
23. The process for preparing 7-[.alpha.-(3-carbamoyl-1-ureido)-.alpha.-phenylacetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-(.alpha.-amino-.alpha.-phenylacetamido)-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid with p-nitrophenylcarbamoyl carbamate.
24. 7-[.alpha.-(3-carbamoyl-1-ureido)-.alpha.-phenylacetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid, whenever prepared by the process of claim 23 or by an obvious chemical equivalent thereof.
25. The process for preparing 7-[.alpha.-(imidazoli-dine-2-one-1-ylcarbonylaminoj-.alpha.-phenylacetamido]-3-)1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-phenylaceta-mido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid with imidazolidine-2-one-1-ylcarbonyl chloride.
26. 7-[.alpha.-(Imidazoliaine-2-one-1-ylcarbonyl-amino)-.alpha.-phenylacetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 25 or by an obvious chemical equivalent thereof.
27. The process for preparing 7-[.alpha.-imidazoli-dine-2-one-1-ylcarbonylamino)-.alpha.-phenylacetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-phenylacetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthio-methyl)-3-cephem-4-carboxylic acid with imidazolidine-2-one-1-ylcarbonyl chloride.
28. 7-[a-(Imidazolidine-2-one-1-ylcarbonylamino-.alpha.-phenylacetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthio-methyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 27 or by an obvious chemical equivalent thereof.
29. The process for preparing 7-[.alpha.-(imidazoli-dine-2-one-1-ylcarbonylamino)-.alpha.-(4-hydroxyphenyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-(4-hydroxy-phenyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid with imidazolidine-2-one-1-ylcarbonyl chloride.
30. 7-[.alpha.-(Imidazolidine-2-one-1-ylcarbonylamino)-.alpha.-(4-hydroxyphenyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid,when prepared by the process of claim 29 or by an obvious chemical equivalent thereof.
31. The process for preparing 7-[.alpha.-(imidazoli-dine-2-one-1-ylcarbonylamino)-.alpha.-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid with imidazoli-dine-2-one-1-ylcarbonyl chloride.
32. 7-[.alpha.-(Imidazolidine-2-one-1-ylcarbonylamino)-.alpha.-(4-hydroxyphenyl)acetamido]-3-(5-methyl-1,3,4-thiadiazole-2-ylthiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 31 or by an obvious chemical equivalent thereof.
33. The process for preparing 7-[.alpha.-[3-(methyl-sulfonyl)imidazoline-.alpha.-one-1-ylcarbonylamino]-.alpha.-(2-thienyl)-acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid which comprises reacting 7-[D-.alpha.-amino-.alpha.-(2-thienyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid with methylsulfonyl-imidazolidine-2-one-1-ylcarbonyl chloride.
34. 7-[.alpha.-[3-(Methylsulfonyl)imidazolidine-2-one-1-ylcarbonylamino]-a-(2-thienyl)acetamido]-3-(1-methyl-1H-tetrazole-5-ylthiomethyl)-3-cephem-4-carboxylic acid, when prepared by the process of claim 33 or by an obvious chemical equivalent thereof.
35. A process for preparing a compound of the formula wherein R" is C1-C3 alkyl; R' is methyl; or R' and R" to-gether with the nitrogen atoms to which they are attached form an imidazolidine-2-one-1-yl ring; R1 is phenyl, hydroxyphenyl, halophenyl, hydroxy substituted halo-phenyl, thienyl or furyl:
which comprises reacting a compound of the formula wherein R1 is as defined above, or a salt thereof,with a compound of the formula wherein R' and R" are as defined above.
which comprises reacting a compound of the formula wherein R1 is as defined above, or a salt thereof,with a compound of the formula wherein R' and R" are as defined above.
36. A compound of the formula wherein R1, R' and R" are as defined in claim 35, wherever prepared by the process of claim 35 or by an obvious chemical equivalent thereof.
37. A process for preparing a compound of the formula wherein R" is C1-C3 alkyl; R' is methyl; or R' and R" to-gether with the nitrogen atoms to which they are attached form an imidazolidine-2-one-1-yl ring; R1 is phenyl, hydroxyphenyl, halophenyl, hydroxy substituted halo-phenyl, thienyl or furyl:
which comprises reacting a compound of the formula wherein R1 is as defined above, or a salt thereof, with a compound of the formula wherein R' and R" are as defined above.
which comprises reacting a compound of the formula wherein R1 is as defined above, or a salt thereof, with a compound of the formula wherein R' and R" are as defined above.
38. A compound of the formula wherein R1, R' and R" are as defined in claim 37, wherever prepared by the process of claim 37 or by an obvious chemical equivalent thereof.
39. A process for preparing a compound of the formula wherein R" is C1-C3 alkyl; R' is methyl; or R' and R" to-gether with the nitrogen atoms to which they are attached form an imidazolidine-2-one-1-yl ring; R1 is phenyl, hydroxyphenyl, halophenyl, hydroxy substituted halo-phenyl, thienyl or furyl: provided when R' and R" are both methyl, R1 is not phenyl;
which comprises reacting a compound of the formula wherein R1 is as defined above, or a salt thereof with a compound of the formula wherein R' and R" are as defined above.
which comprises reacting a compound of the formula wherein R1 is as defined above, or a salt thereof with a compound of the formula wherein R' and R" are as defined above.
40. A compound of the formula wherein R1, R' and R" are as defined in claim 39, wherever prepared by the process of claim 39 or by an obvious chemical equivalent thereof.
41. A process for preparing a compound of the formula which comprises acylating a compound of the formula or a salt thereof with N-chlorocarbonylimidazolidine-2-one.
42. A compound of the formula , whenever prepared by the process of claim 41, or by an obvious chemical equivalent thereof.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US45651674A | 1974-04-01 | 1974-04-01 | |
US456,516 | 1974-04-01 |
Publications (1)
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CA1096373A true CA1096373A (en) | 1981-02-24 |
Family
ID=23813076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA223,530A Expired CA1096373A (en) | 1974-04-01 | 1975-04-01 | Ureido substituted cephalosporin antibiotics |
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JP (1) | JPS614837B2 (en) |
AR (1) | AR210258A1 (en) |
AT (1) | AT337896B (en) |
BE (1) | BE827408A (en) |
BG (1) | BG27376A3 (en) |
CA (1) | CA1096373A (en) |
CH (1) | CH627471A5 (en) |
CS (1) | CS196261B2 (en) |
DD (1) | DD118648A5 (en) |
DE (1) | DE2514019A1 (en) |
DK (1) | DK130375A (en) |
ES (1) | ES436198A1 (en) |
FR (1) | FR2265394B1 (en) |
GB (1) | GB1504589A (en) |
HU (1) | HU170816B (en) |
IE (1) | IE42705B1 (en) |
IL (1) | IL46956A (en) |
NL (1) | NL7503883A (en) |
PH (1) | PH13642A (en) |
PL (1) | PL101400B1 (en) |
RO (1) | RO67392A (en) |
SE (1) | SE423392B (en) |
ZA (1) | ZA752004B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US4063019A (en) | 1976-03-30 | 1977-12-13 | E. R. Squibb & Sons, Inc. | [[[(2,4-Dioxo-1-imidazolidinyl)amino]carbonyl]amino]-acetylcephalosporin derivatives |
CN1069639C (en) * | 1998-06-19 | 2001-08-15 | 山东沂蒙新华制药厂 | Preparation process of 1-chloroformyl-3-mesyl imidazolyl alkyl ketone |
-
1975
- 1975-03-26 DK DK130375A patent/DK130375A/da not_active Application Discontinuation
- 1975-03-28 IL IL46956A patent/IL46956A/en unknown
- 1975-03-28 HU HU75EI00000607A patent/HU170816B/en unknown
- 1975-03-29 DE DE19752514019 patent/DE2514019A1/en not_active Ceased
- 1975-03-29 PL PL1975179227A patent/PL101400B1/en unknown
- 1975-03-29 BG BG029484A patent/BG27376A3/en unknown
- 1975-03-31 RO RO7581853A patent/RO67392A/en unknown
- 1975-03-31 PH PH16988A patent/PH13642A/en unknown
- 1975-04-01 ZA ZA752004A patent/ZA752004B/en unknown
- 1975-04-01 CA CA223,530A patent/CA1096373A/en not_active Expired
- 1975-04-01 JP JP50040203A patent/JPS614837B2/ja not_active Expired
- 1975-04-01 FR FR7510143A patent/FR2265394B1/fr not_active Expired
- 1975-04-01 BE BE1006559A patent/BE827408A/en not_active IP Right Cessation
- 1975-04-01 GB GB13383/75A patent/GB1504589A/en not_active Expired
- 1975-04-01 ES ES436198A patent/ES436198A1/en not_active Expired
- 1975-04-01 NL NL7503883A patent/NL7503883A/en not_active Application Discontinuation
- 1975-04-01 AT AT247675A patent/AT337896B/en not_active IP Right Cessation
- 1975-04-01 CS CS752206A patent/CS196261B2/en unknown
- 1975-04-01 SE SE7503707-7A patent/SE423392B/en unknown
- 1975-04-01 CH CH411575A patent/CH627471A5/en not_active IP Right Cessation
- 1975-04-01 DD DD185120A patent/DD118648A5/xx unknown
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- 1975-04-10 AR AR258200A patent/AR210258A1/en active
Also Published As
Publication number | Publication date |
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BE827408A (en) | 1975-10-01 |
NL7503883A (en) | 1975-10-03 |
RO67392A (en) | 1981-04-30 |
CH627471A5 (en) | 1982-01-15 |
PH13642A (en) | 1980-08-18 |
AU7963775A (en) | 1976-09-30 |
IL46956A (en) | 1979-10-31 |
SE7503707L (en) | 1975-10-02 |
PL101400B1 (en) | 1978-12-30 |
AR210258A1 (en) | 1977-07-15 |
BG27376A3 (en) | 1979-10-12 |
ZA752004B (en) | 1976-11-24 |
AT337896B (en) | 1977-07-25 |
GB1504589A (en) | 1978-03-22 |
DD118648A5 (en) | 1976-03-12 |
SE423392B (en) | 1985-05-03 |
DK130375A (en) | 1975-10-02 |
IE42705L (en) | 1975-10-01 |
JPS614837B2 (en) | 1986-02-13 |
JPS50137995A (en) | 1975-11-01 |
ES436198A1 (en) | 1977-01-01 |
ATA247675A (en) | 1976-11-15 |
CS196261B2 (en) | 1980-03-31 |
FR2265394B1 (en) | 1978-07-28 |
FR2265394A1 (en) | 1975-10-24 |
HU170816B (en) | 1977-09-28 |
IE42705B1 (en) | 1980-10-08 |
IL46956A0 (en) | 1975-05-22 |
DE2514019A1 (en) | 1975-10-02 |
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