GB1505848A - 3,4-dicarboxycephalosporins and derivatives - Google Patents
3,4-dicarboxycephalosporins and derivativesInfo
- Publication number
- GB1505848A GB1505848A GB15803/75A GB1580375A GB1505848A GB 1505848 A GB1505848 A GB 1505848A GB 15803/75 A GB15803/75 A GB 15803/75A GB 1580375 A GB1580375 A GB 1580375A GB 1505848 A GB1505848 A GB 1505848A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- cycloalkyl
- group
- protected
- thienyl
- 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
- -1 1-methyl-1H-tetrazol-5-yl Chemical group 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000004442 acylamino group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 231100000252 nontoxic Toxicity 0.000 abstract 2
- 230000003000 nontoxic effect Effects 0.000 abstract 2
- VWKZOTOKKINGGP-GCZXYKMCSA-N (6r)-3-formyl-8-oxo-7-[(2-thiophen-2-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylic acid Chemical compound C1([C@@H]2N(C1=O)C(C(=CS2)C=O)C(=O)O)NC(=O)CC1=CC=CS1 VWKZOTOKKINGGP-GCZXYKMCSA-N 0.000 abstract 1
- 125000004521 1,3,4-thiadiazol-2-yl group Chemical group S1C(=NN=C1)* 0.000 abstract 1
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000005042 acyloxymethyl group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 abstract 1
- 239000003242 anti bacterial agent Substances 0.000 abstract 1
- 229940088710 antibiotic agent Drugs 0.000 abstract 1
- MKFLFZPSOCGNJJ-PUUKEUDRSA-N benzhydryl (6r)-3-(1,3-dioxolan-2-yl)-8-oxo-7-[(2-thiophen-2-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate Chemical compound S([C@@H]12)C=C(C3OCCO3)C(C(=O)OC(C=3C=CC=CC=3)C=3C=CC=CC=3)N1C(=O)C2NC(=O)CC1=CC=CS1 MKFLFZPSOCGNJJ-PUUKEUDRSA-N 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 abstract 1
- 150000001768 cations Chemical class 0.000 abstract 1
- ZGNIYAPHJAPRMA-UHFFFAOYSA-N chlorine azide Chemical group ClN=[N+]=[N-] ZGNIYAPHJAPRMA-UHFFFAOYSA-N 0.000 abstract 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical group C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 abstract 1
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004970 halomethyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000006502 nitrobenzyl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000003944 tolyl group Chemical group 0.000 abstract 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cephalosporin Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/462,459 US3953436A (en) | 1974-04-19 | 1974-04-19 | 3,4-Dicarboxycephalosporins and derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1505848A true GB1505848A (en) | 1978-03-30 |
Family
ID=23836483
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB15803/75A Expired GB1505848A (en) | 1974-04-19 | 1975-04-17 | 3,4-dicarboxycephalosporins and derivatives |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US3953436A (enExample) |
| JP (1) | JPS50148382A (enExample) |
| AR (4) | AR224221A1 (enExample) |
| AT (1) | AT341669B (enExample) |
| BE (1) | BE828066A (enExample) |
| BG (1) | BG26538A3 (enExample) |
| CA (1) | CA1043332A (enExample) |
| CS (1) | CS195286B2 (enExample) |
| DD (1) | DD118650A5 (enExample) |
| DE (1) | DE2517047A1 (enExample) |
| DK (1) | DK164775A (enExample) |
| ES (4) | ES436737A1 (enExample) |
| FR (1) | FR2267785B1 (enExample) |
| GB (1) | GB1505848A (enExample) |
| HU (1) | HU171887B (enExample) |
| IE (1) | IE41005B1 (enExample) |
| IL (1) | IL47111A (enExample) |
| NL (1) | NL7504607A (enExample) |
| NZ (1) | NZ177260A (enExample) |
| PL (4) | PL103474B1 (enExample) |
| RO (4) | RO69983A (enExample) |
| SE (1) | SE7504535L (enExample) |
| SU (3) | SU735169A3 (enExample) |
| YU (1) | YU98775A (enExample) |
| ZA (1) | ZA752472B (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI760756A7 (enExample) * | 1975-03-26 | 1976-09-27 | Novo Industri As | |
| CN114728008A (zh) * | 2019-08-29 | 2022-07-08 | 加利福尼亚大学董事会 | 鉴定β-内酰胺酶的化合物及其使用方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3864338A (en) * | 1970-08-11 | 1975-02-04 | Squibb & Sons Inc | Process for the preparation of {66 {hu 2{b -cephalosporin aldehydes |
| GB1368235A (en) * | 1970-11-03 | 1974-09-25 | Glaxo Lab Ltd | Azetidinone disulphides and their preparation |
-
1974
- 1974-04-19 US US05/462,459 patent/US3953436A/en not_active Expired - Lifetime
-
1975
- 1975-04-17 JP JP50047380A patent/JPS50148382A/ja active Pending
- 1975-04-17 CA CA224,856A patent/CA1043332A/en not_active Expired
- 1975-04-17 NL NL7504607A patent/NL7504607A/xx not_active Application Discontinuation
- 1975-04-17 FR FR7512026A patent/FR2267785B1/fr not_active Expired
- 1975-04-17 BE BE1006597A patent/BE828066A/xx unknown
- 1975-04-17 DE DE19752517047 patent/DE2517047A1/de not_active Withdrawn
- 1975-04-17 ZA ZA752472A patent/ZA752472B/xx unknown
- 1975-04-17 GB GB15803/75A patent/GB1505848A/en not_active Expired
- 1975-04-17 DK DK164775A patent/DK164775A/da not_active Application Discontinuation
- 1975-04-17 NZ NZ177260A patent/NZ177260A/xx unknown
- 1975-04-18 PL PL1975197696A patent/PL103474B1/pl unknown
- 1975-04-18 SE SE7504535A patent/SE7504535L/xx unknown
- 1975-04-18 ES ES436737A patent/ES436737A1/es not_active Expired
- 1975-04-18 RO RO7591730A patent/RO69983A/ro unknown
- 1975-04-18 AR AR258427A patent/AR224221A1/es active
- 1975-04-18 RO RO7591731A patent/RO70019A/ro unknown
- 1975-04-18 DD DD185554A patent/DD118650A5/xx unknown
- 1975-04-18 HU HU75EI00000614A patent/HU171887B/hu unknown
- 1975-04-18 CS CS752719A patent/CS195286B2/cs unknown
- 1975-04-18 SU SU752127589A patent/SU735169A3/ru active
- 1975-04-18 AT AT299575A patent/AT341669B/de not_active IP Right Cessation
- 1975-04-18 IE IE884/75A patent/IE41005B1/xx unknown
- 1975-04-18 PL PL1975197694A patent/PL103478B1/pl unknown
- 1975-04-18 IL IL47111A patent/IL47111A/xx unknown
- 1975-04-18 YU YU00987/75A patent/YU98775A/xx unknown
- 1975-04-18 PL PL1975179756A patent/PL100075B1/pl unknown
- 1975-04-18 PL PL1975197695A patent/PL103475B1/pl unknown
- 1975-04-18 RO RO7582025A patent/RO66822A/ro unknown
- 1975-04-19 BG BG029721A patent/BG26538A3/xx unknown
- 1975-04-19 RO RO7591729A patent/RO69982A/ro unknown
-
1976
- 1976-05-25 SU SU762361850A patent/SU677663A3/ru active
- 1976-05-27 SU SU762362203A patent/SU639455A3/ru active
- 1976-12-01 ES ES453860A patent/ES453860A1/es not_active Expired
- 1976-12-01 ES ES453859A patent/ES453859A1/es not_active Expired
- 1976-12-01 ES ES453858A patent/ES453858A1/es not_active Expired
- 1976-12-30 AR AR266090A patent/AR218238A1/es active
- 1976-12-30 AR AR266092A patent/AR219910A1/es active
- 1976-12-30 AR AR266091A patent/AR221325A1/es active
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |