IT1209388B - Composizioni antibatteriche e relativi intermedi e procedimenti per la loro preparazione - Google Patents

Composizioni antibatteriche e relativi intermedi e procedimenti per la loro preparazione

Info

Publication number: IT1209388B
Authority: IT; Italy
Prior art keywords: substd; opt; phenyl; alkyl; heterocyclyl
Prior art date: 1979-12-17

Application number

IT5110579A

Other languages

English (en)

Other versions

IT7951105A0 (it

Inventor

Marcel Menard

Alain Martel

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.)

1979-12-17

Filing date

1979-12-17

Publication date

1989-07-16

1979-12-17 Application filed by Bristol Myers Co filed Critical Bristol Myers Co

1979-12-17 Priority to IT5110579A priority Critical patent/IT1209388B/it

1979-12-17 Publication of IT7951105A0 publication Critical patent/IT7951105A0/it

1989-07-16 Application granted granted Critical

1989-07-16 Publication of IT1209388B publication Critical patent/IT1209388B/it

Links

239000003242 anti bacterial agent Substances 0.000 title abstract 2
DUNKKIRUWZSMPT-RXMQYKEDSA-N (5r)-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid Chemical compound OC(=O)C1=CS[C@@H]2CC(=O)N12 DUNKKIRUWZSMPT-RXMQYKEDSA-N 0.000 title 1
125000000217 alkyl group Chemical group 0.000 abstract 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
125000000623 heterocyclic group Chemical group 0.000 abstract 5
229910052736 halogen Inorganic materials 0.000 abstract 4
150000002367 halogens Chemical class 0.000 abstract 4
125000003545 alkoxy group Chemical group 0.000 abstract 3
125000003282 alkyl amino group Chemical group 0.000 abstract 3
MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 3
125000004663 dialkyl amino group Chemical group 0.000 abstract 3
229910006069 SO3H Inorganic materials 0.000 abstract 2
125000004423 acyloxy group Chemical group 0.000 abstract 2
125000005236 alkanoylamino group Chemical group 0.000 abstract 2
125000004414 alkyl thio group Chemical group 0.000 abstract 2
125000002947 alkylene group Chemical group 0.000 abstract 2
125000001589 carboacyl group Chemical group 0.000 abstract 2
125000004043 oxo group Chemical group O=* 0.000 abstract 2
125000001424 substituent group Chemical group 0.000 abstract 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 2
IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 abstract 1
241000894006 Bacteria Species 0.000 abstract 1
-1 COOH alkoxycarbonyl Chemical group 0.000 abstract 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
229910004727 OSO3H Inorganic materials 0.000 abstract 1
125000001931 aliphatic group Chemical group 0.000 abstract 1
125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 1
125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
239000003795 chemical substances by application Substances 0.000 abstract 1
125000005117 dialkylcarbamoyl group Chemical group 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
125000001188 haloalkyl group Chemical group 0.000 abstract 1
125000005844 heterocyclyloxy group Chemical group 0.000 abstract 1
125000004468 heterocyclylthio group Chemical group 0.000 abstract 1
239000000543 intermediate Substances 0.000 abstract 1
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 abstract 1
HHXMXAQDOUCLDN-RXMQYKEDSA-N penem Chemical compound S1C=CN2C(=O)C[C@H]21 HHXMXAQDOUCLDN-RXMQYKEDSA-N 0.000 abstract 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
125000003884 phenylalkyl group Chemical group 0.000 abstract 1
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 abstract 1
150000003839 salts Chemical class 0.000 abstract 1
125000000464 thioxo group Chemical group S=* 0.000 abstract 1

Landscapes

Nitrogen Condensed Heterocyclic Rings (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

IT5110579A 1979-12-17 1979-12-17 Composizioni antibatteriche e relativi intermedi e procedimenti per la loro preparazione IT1209388B (it)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
IT5110579A IT1209388B (it)	1979-12-17	1979-12-17	Composizioni antibatteriche e relativi intermedi e procedimenti per la loro preparazione

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT5110579A IT1209388B (it)	1979-12-17	1979-12-17	Composizioni antibatteriche e relativi intermedi e procedimenti per la loro preparazione

Publications (2)

Publication Number	Publication Date
IT7951105A0 IT7951105A0 (it)	1979-12-17
IT1209388B true IT1209388B (it)	1989-07-16

Family

ID=11274389

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IT5110579A IT1209388B (it)	1979-12-17	1979-12-17	Composizioni antibatteriche e relativi intermedi e procedimenti per la loro preparazione

Country Status (1)

Country	Link
IT (1)	IT1209388B (it)

1979
- 1979-12-17 IT IT5110579A patent/IT1209388B/it active

Also Published As

Publication number	Publication date
IT7951105A0 (it)	1979-12-17

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