GB1444224A - Cephalosporin compounds' - Google Patents
Cephalosporin compounds'Info
- Publication number
- GB1444224A GB1444224A GB3429772A GB3429772A GB1444224A GB 1444224 A GB1444224 A GB 1444224A GB 3429772 A GB3429772 A GB 3429772A GB 3429772 A GB3429772 A GB 3429772A GB 1444224 A GB1444224 A GB 1444224A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- alkyl
- compound
- aryl
- amino
- 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
- 229930186147 Cephalosporin Natural products 0.000 title abstract 5
- 229940124587 cephalosporin Drugs 0.000 title abstract 5
- -1 Cephalosporin compounds Chemical class 0.000 title abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 229910052751 metal Inorganic materials 0.000 abstract 4
- 239000002184 metal Substances 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 150000001780 cephalosporins Chemical class 0.000 abstract 3
- 150000002431 hydrogen Chemical class 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 239000007858 starting material Substances 0.000 abstract 3
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 abstract 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 230000000903 blocking effect Effects 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052723 transition metal Inorganic materials 0.000 abstract 2
- 150000003624 transition metals Chemical class 0.000 abstract 2
- FZEVMBJWXHDLDB-ZCFIWIBFSA-N (6r)-5-thia-1-azabicyclo[4.2.0]oct-2-en-8-one Chemical compound S1CC=CN2C(=O)C[C@H]21 FZEVMBJWXHDLDB-ZCFIWIBFSA-N 0.000 abstract 1
- SXBDXXFTJVHSAF-ZCFIWIBFSA-N (6r)-5-thia-1-azabicyclo[4.2.0]oct-3-en-8-one Chemical compound S1C=CCN2C(=O)C[C@H]21 SXBDXXFTJVHSAF-ZCFIWIBFSA-N 0.000 abstract 1
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 abstract 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- RHOCAKCKESHZJJ-OXQOHEQNSA-N benzhydryl (6r,7r)-7-amino-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chemical compound S([C@H]1N2C([C@H]1N)=O)CC(C)=C2C(=O)OC(C=1C=CC=CC=1)C1=CC=CC=C1 RHOCAKCKESHZJJ-OXQOHEQNSA-N 0.000 abstract 1
- 229910052793 cadmium Inorganic materials 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- MPMSMUBQXQALQI-UHFFFAOYSA-N cobalt phthalocyanine Chemical class [Co+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 MPMSMUBQXQALQI-UHFFFAOYSA-N 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- VRLDVERQJMEPIF-UHFFFAOYSA-N dbdmh Chemical compound CC1(C)N(Br)C(=O)N(Br)C1=O VRLDVERQJMEPIF-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
- 125000005883 dithianyl group Chemical group 0.000 abstract 1
- 125000005411 dithiolanyl group Chemical group S1SC(CC1)* 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 229910052748 manganese Inorganic materials 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
Landscapes
- Cephalosporin Compounds (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3429772A GB1444224A (en) | 1972-07-21 | 1972-07-21 | Cephalosporin compounds' |
| BE133700A BE802605A (fr) | 1972-07-21 | 1973-07-20 | Procede de preparation de derives de cephalosporine et nouveaux composes obtenus |
| FR7326801A FR2199540B1 (enExample) | 1972-07-21 | 1973-07-20 | |
| CH1071173A CH601307A5 (enExample) | 1972-07-21 | 1973-07-20 | |
| IE124273A IE37939B1 (en) | 1972-07-21 | 1973-07-20 | Improvements in or relating to cephalosporin compounds |
| LU68063D LU68063A1 (enExample) | 1972-07-21 | 1973-07-20 | |
| NL7310122A NL7310122A (enExample) | 1972-07-21 | 1973-07-20 | |
| AT643173A AT335058B (de) | 1972-07-21 | 1973-07-20 | Verfahren zur herstellung von 3-athyl- und 3-subst. athylcephalosporinverbindungen |
| DE19732337047 DE2337047A1 (de) | 1972-07-21 | 1973-07-20 | Neue cephalosporinverbindungen und verfahren zu ihrer herstellung |
| JP8248273A JPS4985090A (enExample) | 1972-07-21 | 1973-07-20 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3429772A GB1444224A (en) | 1972-07-21 | 1972-07-21 | Cephalosporin compounds' |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1444224A true GB1444224A (en) | 1976-07-28 |
Family
ID=10363867
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3429772A Expired GB1444224A (en) | 1972-07-21 | 1972-07-21 | Cephalosporin compounds' |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS4985090A (enExample) |
| AT (1) | AT335058B (enExample) |
| BE (1) | BE802605A (enExample) |
| CH (1) | CH601307A5 (enExample) |
| DE (1) | DE2337047A1 (enExample) |
| FR (1) | FR2199540B1 (enExample) |
| GB (1) | GB1444224A (enExample) |
| IE (1) | IE37939B1 (enExample) |
| LU (1) | LU68063A1 (enExample) |
| NL (1) | NL7310122A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5043439A (en) * | 1990-03-08 | 1991-08-27 | Bristol-Myers Squibb Company | Process for production of cephalosporins |
-
1972
- 1972-07-21 GB GB3429772A patent/GB1444224A/en not_active Expired
-
1973
- 1973-07-20 JP JP8248273A patent/JPS4985090A/ja active Pending
- 1973-07-20 AT AT643173A patent/AT335058B/de not_active IP Right Cessation
- 1973-07-20 CH CH1071173A patent/CH601307A5/xx not_active IP Right Cessation
- 1973-07-20 IE IE124273A patent/IE37939B1/xx unknown
- 1973-07-20 DE DE19732337047 patent/DE2337047A1/de active Pending
- 1973-07-20 NL NL7310122A patent/NL7310122A/xx not_active Application Discontinuation
- 1973-07-20 LU LU68063D patent/LU68063A1/xx unknown
- 1973-07-20 FR FR7326801A patent/FR2199540B1/fr not_active Expired
- 1973-07-20 BE BE133700A patent/BE802605A/xx unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5043439A (en) * | 1990-03-08 | 1991-08-27 | Bristol-Myers Squibb Company | Process for production of cephalosporins |
| GR910100112A (en) * | 1990-03-08 | 1992-06-30 | Bristol Myers Squibb Co | Organo cuprate process for cefprozil |
Also Published As
| Publication number | Publication date |
|---|---|
| ATA643173A (de) | 1976-06-15 |
| JPS4985090A (enExample) | 1974-08-15 |
| CH601307A5 (enExample) | 1978-07-14 |
| DE2337047A1 (de) | 1974-01-31 |
| NL7310122A (enExample) | 1974-01-23 |
| BE802605A (fr) | 1974-01-21 |
| IE37939L (en) | 1974-01-21 |
| AT335058B (de) | 1977-02-25 |
| LU68063A1 (enExample) | 1973-09-26 |
| IE37939B1 (en) | 1977-11-23 |
| FR2199540B1 (enExample) | 1978-05-26 |
| FR2199540A1 (enExample) | 1974-04-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 48S | Specification amended (sect. 8/1949) | ||
| PS | Patent sealed | ||
| SP | Amendment (slips) printed | ||
| PCNP | Patent ceased through non-payment of renewal fee |