GB873049A - Improvements in or relating to penicillin derivatives - Google Patents
Improvements in or relating to penicillin derivativesInfo
- Publication number
- GB873049A GB873049A GB31847/58A GB3184758A GB873049A GB 873049 A GB873049 A GB 873049A GB 31847/58 A GB31847/58 A GB 31847/58A GB 3184758 A GB3184758 A GB 3184758A GB 873049 A GB873049 A GB 873049A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- substituted
- penicillin
- group
- 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
- 150000002960 penicillins Chemical class 0.000 title abstract 5
- 229930182555 Penicillin Natural products 0.000 abstract 6
- 150000003839 salts Chemical class 0.000 abstract 5
- 125000003277 amino group Chemical group 0.000 abstract 4
- 125000006239 protecting group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- -1 amino, carboxyl Chemical group 0.000 abstract 3
- 229940049954 penicillin Drugs 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 2
- 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 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 231100000252 nontoxic Toxicity 0.000 abstract 2
- 230000003000 nontoxic effect Effects 0.000 abstract 2
- NGHVIOIJCVXTGV-UHFFFAOYSA-N 6beta-amino-penicillanic acid Natural products OC(=O)C1C(C)(C)SC2C(N)C(=O)N21 NGHVIOIJCVXTGV-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- BWLUMTFWVZZZND-UHFFFAOYSA-N Dibenzylamine Chemical class C=1C=CC=CC=1CNCC1=CC=CC=C1 BWLUMTFWVZZZND-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- JVVXZOOGOGPDRZ-SLFFLAALSA-N [(1R,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]methanamine Chemical compound NC[C@]1(C)CCC[C@]2(C)C3=CC=C(C(C)C)C=C3CC[C@H]21 JVVXZOOGOGPDRZ-SLFFLAALSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical class 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- 150000003863 ammonium salts Chemical class 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- UPABQMWFWCMOFV-UHFFFAOYSA-N benethamine Chemical class C=1C=CC=CC=1CNCCC1=CC=CC=C1 UPABQMWFWCMOFV-UHFFFAOYSA-N 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 abstract 1
- 125000000068 chlorophenyl group Chemical group 0.000 abstract 1
- 229960004244 cyclacillin Drugs 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 230000006378 damage Effects 0.000 abstract 1
- 150000004985 diamines Chemical class 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 229910052763 palladium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical class CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 abstract 1
- 229960004919 procaine Drugs 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 125000005270 trialkylamine group Chemical class 0.000 abstract 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[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
- C07D499/21—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 with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
- C07D499/44—Compounds with an amino radical acylated by carboxylic acids, attached in position 6
- C07D499/48—Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical
- C07D499/58—Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical
- C07D499/64—Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical by nitrogen atoms
- C07D499/68—Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical by nitrogen atoms with aromatic rings as additional substituents on the carbon chain
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D499/21—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 with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
- C07D499/44—Compounds with an amino radical acylated by carboxylic acids, attached in position 6
- C07D499/48—Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB31847/58A GB873049A (en) | 1958-10-06 | 1958-10-06 | Improvements in or relating to penicillin derivatives |
ES0252422A ES252422A1 (es) | 1958-10-06 | 1959-10-02 | Proceso para la preparaciën de derivados penicilinicos de la fërmula general: |
FR806723A FR246M (enrdf_load_stackoverflow) | 1958-10-06 | 1959-10-05 | |
NO133325A NO115737B (enrdf_load_stackoverflow) | 1958-10-06 | 1959-10-05 | |
DK356359AA DK126118B (da) | 1958-10-06 | 1959-10-06 | Fremgangsmåde til fremstilling af 6-aminopenicillansyrederivater eller salte deraf. |
CH7907859A CH387635A (de) | 1958-10-06 | 1959-10-06 | Verfahren zur Herstellung von Penicillinen |
CH638961A CH407126A (de) | 1958-10-06 | 1961-06-01 | Verfahren zur Herstellung von epimeren a-Amino-benzylpenicillinen |
FR863883A FR12F (fr) | 1958-10-06 | 1961-06-05 | Dérivés de la pénicilline et leur procédé de préparation. |
CY24262A CY242A (en) | 1958-10-06 | 1962-07-03 | Improvements in or relating to penicillin derivatives |
GB4154162A GB978178A (en) | 1958-10-06 | 1962-11-02 | Penicillins |
MY6200044A MY6200044A (en) | 1958-10-06 | 1962-12-31 | Improvements in or relating to penicillin derivatives |
OA50915A OA00880A (fr) | 1958-10-06 | 1964-12-18 | Dérivés de la pénicélline et leur procédé de préparation. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB31847/58A GB873049A (en) | 1958-10-06 | 1958-10-06 | Improvements in or relating to penicillin derivatives |
GB1630359 | 1959-05-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB873049A true GB873049A (en) | 1961-07-19 |
Family
ID=26251956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31847/58A Expired GB873049A (en) | 1958-10-06 | 1958-10-06 | Improvements in or relating to penicillin derivatives |
Country Status (8)
Country | Link |
---|---|
CH (1) | CH387635A (enrdf_load_stackoverflow) |
CY (1) | CY242A (enrdf_load_stackoverflow) |
DK (1) | DK126118B (enrdf_load_stackoverflow) |
ES (1) | ES252422A1 (enrdf_load_stackoverflow) |
FR (1) | FR246M (enrdf_load_stackoverflow) |
GB (1) | GB873049A (enrdf_load_stackoverflow) |
NO (1) | NO115737B (enrdf_load_stackoverflow) |
OA (1) | OA00880A (enrdf_load_stackoverflow) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK104060C (da) * | 1962-08-18 | 1966-03-28 | Beecham Res Lab | Fremgangsmåde til fremstilling af α-aminobenzylpenicillin eller salte deraf. |
US3245984A (en) * | 1961-09-26 | 1966-04-12 | Lepetit Spa | Amino-alpha-phenylalkyl penicillins |
DE1296142B (de) * | 1962-01-29 | 1969-05-29 | Bristol Myers Co | Verfahren zur Herstellung von ª‡-Aminobenzylpenicillin |
EP0477639A1 (de) * | 1990-09-22 | 1992-04-01 | Bayer Ag | Substituierte Aminosäureamid-Derivate deren Herstellung und Verwendung |
US5158962A (en) * | 1989-11-01 | 1992-10-27 | Bayer Aktiengesellschaft | Fungicidal substituted amino acid amides |
US5723646A (en) * | 1991-01-24 | 1998-03-03 | Bayer Aktiengesellschaft | Substituted amino acid amide derivatives their preparation and use as fungicides |
-
1958
- 1958-10-06 GB GB31847/58A patent/GB873049A/en not_active Expired
-
1959
- 1959-10-02 ES ES0252422A patent/ES252422A1/es not_active Expired
- 1959-10-05 NO NO133325A patent/NO115737B/no unknown
- 1959-10-05 FR FR806723A patent/FR246M/fr not_active Expired
- 1959-10-06 DK DK356359AA patent/DK126118B/da unknown
- 1959-10-06 CH CH7907859A patent/CH387635A/de unknown
-
1962
- 1962-07-03 CY CY24262A patent/CY242A/xx unknown
-
1964
- 1964-12-18 OA OA50915A patent/OA00880A/xx unknown
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3245984A (en) * | 1961-09-26 | 1966-04-12 | Lepetit Spa | Amino-alpha-phenylalkyl penicillins |
DE1296142B (de) * | 1962-01-29 | 1969-05-29 | Bristol Myers Co | Verfahren zur Herstellung von ª‡-Aminobenzylpenicillin |
DK104060C (da) * | 1962-08-18 | 1966-03-28 | Beecham Res Lab | Fremgangsmåde til fremstilling af α-aminobenzylpenicillin eller salte deraf. |
US5158962A (en) * | 1989-11-01 | 1992-10-27 | Bayer Aktiengesellschaft | Fungicidal substituted amino acid amides |
EP0477639A1 (de) * | 1990-09-22 | 1992-04-01 | Bayer Ag | Substituierte Aminosäureamid-Derivate deren Herstellung und Verwendung |
US5723646A (en) * | 1991-01-24 | 1998-03-03 | Bayer Aktiengesellschaft | Substituted amino acid amide derivatives their preparation and use as fungicides |
US5942541A (en) * | 1991-01-24 | 1999-08-24 | Bayer Aktiengesellschaft | Substituted amino acid amide derivatives their preparation and use as fungicides |
Also Published As
Publication number | Publication date |
---|---|
FR246M (enrdf_load_stackoverflow) | 1900-01-01 |
NO115737B (enrdf_load_stackoverflow) | 1968-11-25 |
OA00880A (fr) | 1968-03-22 |
CH387635A (de) | 1965-02-15 |
DK126118B (da) | 1973-06-12 |
ES252422A1 (es) | 1960-01-01 |
CY242A (en) | 1962-07-03 |
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