GB1290177A - - Google Patents
Info
- Publication number
- GB1290177A GB1290177A GB1290177DA GB1290177A GB 1290177 A GB1290177 A GB 1290177A GB 1290177D A GB1290177D A GB 1290177DA GB 1290177 A GB1290177 A GB 1290177A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- alkoxy
- carbo
- phenyl
- formula
- 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
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 125000003545 alkoxy group Chemical group 0.000 abstract 9
- -1 carboxyvinyl Chemical group 0.000 abstract 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 4
- 229930182555 Penicillin Natural products 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- 150000002960 penicillins Chemical class 0.000 abstract 2
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 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 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- 241000894006 Bacteria Species 0.000 abstract 1
- IYXGSMUGOJNHAZ-UHFFFAOYSA-N Ethyl malonate Chemical class CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 230000003115 biocidal effect Effects 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 231100000252 nontoxic Toxicity 0.000 abstract 1
- 230000003000 nontoxic effect Effects 0.000 abstract 1
- 235000010292 orthophenyl phenol Nutrition 0.000 abstract 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 abstract 1
- 229940049954 penicillin Drugs 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229960003424 phenylacetic acid Drugs 0.000 abstract 1
- 239000003279 phenylacetic acid Substances 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- WWYDYZMNFQIYPT-UHFFFAOYSA-N ru78191 Chemical compound OC(=O)C(C(O)=O)C1=CC=CC=C1 WWYDYZMNFQIYPT-UHFFFAOYSA-N 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/30—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings
- C07C57/34—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings containing more than one carboxyl group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83051769A | 1969-06-04 | 1969-06-04 | |
US83051669A | 1969-06-04 | 1969-06-04 | |
US83048169A | 1969-06-04 | 1969-06-04 | |
US83051869A | 1969-06-04 | 1969-06-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1290177A true GB1290177A (enrdf_load_stackoverflow) | 1972-09-20 |
Family
ID=27505879
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1290177D Expired GB1290177A (enrdf_load_stackoverflow) | 1969-06-04 | 1969-08-29 |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB1290177A (enrdf_load_stackoverflow) |
MY (1) | MY7400195A (enrdf_load_stackoverflow) |
-
1969
- 1969-08-29 GB GB1290177D patent/GB1290177A/en not_active Expired
-
1974
- 1974-12-30 MY MY7400195A patent/MY7400195A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
MY7400195A (en) | 1974-12-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1526978A (en) | 3-thiosubstituted cephalosporin antibiotics | |
GB1505885A (en) | Substituted cephalosporins | |
GB1289358A (enrdf_load_stackoverflow) | ||
ES8602705A1 (es) | Un procedimiento para la preparacion de un compuesto. | |
GB1268708A (en) | Acylation process | |
US4263292A (en) | 7α-methoxycephalosporins and pharmaceutical composition comprising the same | |
GB1290177A (enrdf_load_stackoverflow) | ||
DE2857696C2 (de) | Cephalosporine | |
GB1457484A (en) | Acylamidocephalosporins | |
US4160830A (en) | Cephalosporins | |
ES429864A1 (es) | Procedimiento para la obtencion de derivados cefem. | |
GB1421279A (en) | 3-heterocyclicthiomethylcephalosporins | |
GB1436977A (en) | 7-alkylthioacetamido cephaosporins | |
GB1293590A (en) | New penicillanic acid derivatives | |
GB1304202A (enrdf_load_stackoverflow) | ||
CA1136615A (en) | 7.alpha.-METHOXYCEPHALOSPORINS AND PROCESS FOR PRODUCING THE SAME | |
GB1335403A (en) | Pharmaceutical compositions containing benzofuran derivatives | |
FR2205515B1 (enrdf_load_stackoverflow) | ||
JPH0530836B2 (enrdf_load_stackoverflow) | ||
AT368164B (de) | Verfahren zur herstellung von neuen 7alphamethoxycephalosporinen | |
JPH0121152B2 (enrdf_load_stackoverflow) | ||
IE36558L (en) | Esterification of penicillins | |
GB1398564A (en) | 1-amino substituted-1-cycloalkane derivatives of 6-amino penicillanic acid | |
GB1410852A (en) | Substituted 4-biphenylyl-butenoic acids esters and amides and pharmaceutical compositions containing them | |
GB1410303A (en) | Piperazinyl-butanol derivatives |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PE20 | Patent expired after termination of 20 years |