ES295651A1 - Un procedimiento para la preparación de un nuevo compuesto antibacterial - Google Patents

Un procedimiento para la preparación de un nuevo compuesto antibacterial

Info

Publication number: ES295651A1
Authority: ES; Spain
Prior art keywords: alkyl; group; belonging; translation; formula
Prior art date: 1963-01-25
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

Application number

ES295651A

Other languages

English (en)

Spanish (es)

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bristol Myers Co

Original Assignee

Bristol Myers Co

Priority date (The priority date 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 date listed.)

1963-01-25

Filing date

1964-01-23

Publication date

1964-10-16

1964-01-23 Application filed by Bristol Myers Co filed Critical Bristol Myers Co

1964-10-16 Publication of ES295651A1 publication Critical patent/ES295651A1/es

Status Expired legal-status Critical Current

Links

230000000844 anti-bacterial effect Effects 0.000 title abstract 2
150000001875 compounds Chemical class 0.000 title abstract 2
238000000034 method Methods 0.000 title abstract 2
125000000217 alkyl group Chemical group 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
125000001589 carboacyl group Chemical group 0.000 abstract 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
125000004435 hydrogen atom Chemical class [H]* 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
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 abstract 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
229930182555 Penicillin Natural products 0.000 abstract 1
239000002253 acid Substances 0.000 abstract 1
150000007513 acids Chemical class 0.000 abstract 1
150000001299 aldehydes Chemical class 0.000 abstract 1
125000003545 alkoxy group Chemical group 0.000 abstract 1
125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
-1 alkyl ketones Chemical class 0.000 abstract 1
125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
125000004414 alkyl thio group Chemical group 0.000 abstract 1
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 abstract 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
229910052794 bromium Inorganic materials 0.000 abstract 1
150000001728 carbonyl compounds Chemical class 0.000 abstract 1
239000007795 chemical reaction product Substances 0.000 abstract 1
229910052801 chlorine Inorganic materials 0.000 abstract 1
239000000460 chlorine Substances 0.000 abstract 1
125000000753 cycloalkyl group Chemical group 0.000 abstract 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 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
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
125000001153 fluoro group Chemical group F* 0.000 abstract 1
125000002541 furyl group Chemical group 0.000 abstract 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
125000001624 naphthyl group Chemical group 0.000 abstract 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
231100000252 nontoxic Toxicity 0.000 abstract 1
230000003000 nontoxic effect Effects 0.000 abstract 1
150000002960 penicillins Chemical class 0.000 abstract 1
150000003254 radicals Chemical class 0.000 abstract 1
238000011084 recovery Methods 0.000 abstract 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Cylinder Crankcases Of Internal Combustion Engines (AREA)
Combustion Methods Of Internal-Combustion Engines (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

ES295651A 1963-01-25 1964-01-23 Un procedimiento para la preparación de un nuevo compuesto antibacterial Expired ES295651A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US25399563A	1963-01-25	1963-01-25

Publications (1)

Publication Number	Publication Date
ES295651A1 true ES295651A1 (es)	1964-10-16

Family

ID=22962515

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES295651A Expired ES295651A1 (es)	1963-01-25	1964-01-23	Un procedimiento para la preparación de un nuevo compuesto antibacterial

Country Status (14)

Country	Link
AT (1)	AT248022B (fr)
CH (1)	CH448093A (fr)
CY (1)	CY712A (fr)
DE (1)	DE1445517B2 (fr)
DK (1)	DK119163B (fr)
ES (1)	ES295651A1 (fr)
FI (1)	FI48194C (fr)
FR (1)	FR3333M (fr)
GB (1)	GB1057654A (fr)
MY (1)	MY7300505A (fr)
NL (2)	NL6400559A (fr)
NO (1)	NO135066C (fr)
OA (1)	OA00997A (fr)
SE (1)	SE318276B (fr)

0
- NL NL129435D patent/NL129435C/xx active
1964
- 1964-01-21 AT AT44764A patent/AT248022B/de active
- 1964-01-21 DE DE1964B0075082 patent/DE1445517B2/de active Granted
- 1964-01-22 CH CH70964A patent/CH448093A/de unknown
- 1964-01-23 ES ES295651A patent/ES295651A1/es not_active Expired
- 1964-01-23 SE SE808/64A patent/SE318276B/xx unknown
- 1964-01-23 DK DK34264AA patent/DK119163B/da unknown
- 1964-01-24 NO NO151720A patent/NO135066C/no unknown
- 1964-01-24 FI FI640141A patent/FI48194C/fi active
- 1964-01-24 GB GB3251/64A patent/GB1057654A/en not_active Expired
- 1964-01-24 NL NL6400559A patent/NL6400559A/xx unknown
- 1964-04-23 FR FR972084A patent/FR3333M/fr active Active
- 1964-12-29 OA OA51100A patent/OA00997A/fr unknown
1973
- 1973-11-06 CY CY71273A patent/CY712A/xx unknown
- 1973-12-31 MY MY1973505A patent/MY7300505A/xx unknown

Also Published As

Publication number	Publication date
DE1445517B2 (de)	1976-06-10
DK119163B (da)	1970-11-23
NO135066C (fr)	1977-02-02
FI48194B (fr)	1974-04-01
OA00997A (fr)	1968-08-07
NL6400559A (fr)	1964-07-27
CY712A (en)	1973-11-06
SE318276B (fr)	1969-12-08
NL129435C (fr)
FI48194C (fi)	1974-07-10
CH448093A (de)	1967-12-15
GB1057654A (en)	1967-02-08
DE1445517A1 (de)	1969-09-25
FR3333M (fr)	1965-05-24
AT248022B (de)	1966-07-11
MY7300505A (en)	1973-12-31
NO135066B (fr)	1976-10-25

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