SE7709583L - 2,3-legre alkylenpenam-3-karboxylsyraderivat samt forfarande for framstellning derav - Google Patents

2,3-legre alkylenpenam-3-karboxylsyraderivat samt forfarande for framstellning derav

Info

Publication number: SE7709583L
Authority: SE; Sweden
Prior art keywords: alkanoylamino; substituted; phenyl; group; compounds
Prior art date: 1972-11-22

Application number

SE7709583A

Other languages

Unknown language ( )

English (en)

Inventor

T Kamiya

T Teraji

M Hashimoto

O Nakaguti

T Oku

Original Assignee

Fujisawa Pharmaceutical 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.)

1972-11-22

Filing date

1977-08-25

Publication date

1977-08-25

1972-11-22 Priority claimed from JP11738572A external-priority patent/JPS5727114B2/ja

1972-11-27 Priority claimed from JP11911372A external-priority patent/JPS5727115B2/ja

1972-12-15 Priority claimed from JP12663672A external-priority patent/JPS5535397B2/ja

1973-08-02 Priority claimed from JP8785473A external-priority patent/JPS5643471B2/ja

1973-08-02 Priority claimed from JP8785173A external-priority patent/JPS5641635B2/ja

1973-08-02 Priority claimed from JP8785573A external-priority patent/JPS5643472B2/ja

1977-08-25 Application filed by Fujisawa Pharmaceutical Co filed Critical Fujisawa Pharmaceutical Co

1977-08-25 Publication of SE7709583L publication Critical patent/SE7709583L/sv

Links

238000000034 method Methods 0.000 title abstract 3
125000005236 alkanoylamino group Chemical group 0.000 abstract 14
150000001875 compounds Chemical class 0.000 abstract 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 7
125000003277 amino group Chemical group 0.000 abstract 3
239000003795 chemical substances by application Substances 0.000 abstract 3
150000003839 salts Chemical class 0.000 abstract 3
125000006624 (C1-C6) alkoxycarbonylamino group Chemical group 0.000 abstract 2
-1 3-phenylureido, phenylglyoxylamido, phenylthiocarbamoylamino, phenyl Chemical group 0.000 abstract 2
125000003118 aryl group Chemical group 0.000 abstract 2
238000006243 chemical reaction Methods 0.000 abstract 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
239000002904 solvent Substances 0.000 abstract 2
125000003107 substituted aryl group Chemical group 0.000 abstract 2
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
239000002253 acid Substances 0.000 abstract 1
150000008065 acid anhydrides Chemical class 0.000 abstract 1
125000002252 acyl group Chemical group 0.000 abstract 1
125000004442 acylamino group Chemical group 0.000 abstract 1
230000010933 acylation Effects 0.000 abstract 1
238000005917 acylation reaction Methods 0.000 abstract 1
125000004423 acyloxy group Chemical group 0.000 abstract 1
125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 1
125000002947 alkylene group Chemical group 0.000 abstract 1
150000001408 amides Chemical class 0.000 abstract 1
150000001412 amines Chemical class 0.000 abstract 1
230000000845 anti-microbial effect Effects 0.000 abstract 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
125000002843 carboxylic acid group Chemical group 0.000 abstract 1
238000007796 conventional method Methods 0.000 abstract 1
150000002148 esters Chemical class 0.000 abstract 1
125000005059 halophenyl group Chemical group 0.000 abstract 1
125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
239000007788 liquid Substances 0.000 abstract 1
230000001590 oxidative effect Effects 0.000 abstract 1
239000008194 pharmaceutical composition Substances 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
125000005544 phthalimido group Chemical group 0.000 abstract 1
125000006239 protecting group Chemical group 0.000 abstract 1
230000001681 protective effect Effects 0.000 abstract 1
DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 abstract 1
239000007858 starting material Substances 0.000 abstract 1
125000003831 tetrazolyl group Chemical group 0.000 abstract 1
125000001113 thiadiazolyl group Chemical group 0.000 abstract 1
125000001544 thienyl group Chemical group 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
- C07D499/04—Preparation
- 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
- 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)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Cephalosporin Compounds (AREA)

SE7709583A 1972-11-22 1977-08-25 2,3-legre alkylenpenam-3-karboxylsyraderivat samt forfarande for framstellning derav SE7709583L (sv)

Applications Claiming Priority (6)

Application Number	Priority Date	Filing Date
JP11738572A JPS5727114B2 (sv)	1972-11-22	1972-11-22
JP11911372A JPS5727115B2 (sv)	1972-11-27	1972-11-27
JP12663672A JPS5535397B2 (sv)	1972-12-15	1972-12-15
JP8785473A JPS5643471B2 (sv)	1973-08-02	1973-08-02
JP8785173A JPS5641635B2 (sv)	1973-08-02	1973-08-02
JP8785573A JPS5643472B2 (sv)	1973-08-02	1973-08-02

Publications (1)

Publication Number	Publication Date
SE7709583L true SE7709583L (sv)	1977-08-25

Family

ID=27551725

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
SE7315773A SE416654B (sv)	1972-11-22	1973-11-21	Forfarande for framstellning av 2,3-legre alkylenpenam-3-karboxylsyraderivat
SE7709583A SE7709583L (sv)	1972-11-22	1977-08-25	2,3-legre alkylenpenam-3-karboxylsyraderivat samt forfarande for framstellning derav

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
SE7315773A SE416654B (sv)	1972-11-22	1973-11-21	Forfarande for framstellning av 2,3-legre alkylenpenam-3-karboxylsyraderivat

Country Status (11)

Country	Link
US (1)	US3904607A (sv)
CA (1)	CA1026746A (sv)
CH (1)	CH599219A5 (sv)
DE (1)	DE2358178C2 (sv)
FI (1)	FI793327A7 (sv)
FR (1)	FR2207696B1 (sv)
GB (1)	GB1455693A (sv)
HU (1)	HU169066B (sv)
NL (1)	NL7316005A (sv)
NO (2)	NO750470L (sv)
SE (2)	SE416654B (sv)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1576414A (en) *	1976-05-25	1980-10-08	Ucb Sa	Anti-bacterially-active penicillins

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3466275A (en) *	1962-07-31	1969-09-09	Lilly Co Eli	Modified penicillins and their preparation via penicillin sulfoxides

1973
- 1973-11-14 GB GB5175973A patent/GB1455693A/en not_active Expired
- 1973-11-19 CH CH1621373A patent/CH599219A5/xx not_active IP Right Cessation
- 1973-11-21 FR FR7341464A patent/FR2207696B1/fr not_active Expired
- 1973-11-21 HU HUFU321A patent/HU169066B/hu unknown
- 1973-11-21 SE SE7315773A patent/SE416654B/sv unknown
- 1973-11-21 CA CA186,418A patent/CA1026746A/en not_active Expired
- 1973-11-22 DE DE2358178A patent/DE2358178C2/de not_active Expired
- 1973-11-22 NL NL7316005A patent/NL7316005A/xx not_active Application Discontinuation
- 1973-11-23 US US418259A patent/US3904607A/en not_active Expired - Lifetime
1975
- 1975-02-13 NO NO750470A patent/NO750470L/no unknown
- 1975-02-13 NO NO750471A patent/NO750471L/no unknown
1977
- 1977-08-25 SE SE7709583A patent/SE7709583L/sv not_active Application Discontinuation
1979
- 1979-10-25 FI FI793327A patent/FI793327A7/sv not_active Application Discontinuation

Also Published As

Publication number	Publication date
HU169066B (sv)	1976-09-28
SE416654B (sv)	1981-01-26
NO750471L (sv)	1974-05-24
AU6277673A (en)	1975-05-22
GB1455693A (en)	1976-11-17
CH599219A5 (sv)	1978-05-12
US3904607A (en)	1975-09-09
NO750470L (sv)	1974-05-24
FR2207696A1 (sv)	1974-06-21
FI793327A7 (sv)	1981-01-01
DE2358178C2 (de)	1985-06-27
DE2358178A1 (de)	1974-05-30
FR2207696B1 (sv)	1977-04-22
NL7316005A (sv)	1974-05-27
CA1026746A (en)	1978-02-21

Legal Events

Date

Code

Title

Description

1995-02-28

NAV

Patent application has lapsed

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DD212510B3 (de)	1989-11-08	Verfahren zur herstellung von 1-sulfo-2-azetidinon-derivaten
IE37767B1 (en)	1977-10-12	Derivatives of 7beta-amino-cephem-3-ol-4-carboxylic acids
GB1291675A (en)	1972-10-04	0-(1,3,4-thiadiazol-2-yl)-imidazolidinone(2) derivatives, process for their production and their use as herbicidal agents
JPS587637B2 (ja)	1983-02-10	シンキペニシリンノセイホウ
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SE7709583L (sv)	1977-08-25	2,3-legre alkylenpenam-3-karboxylsyraderivat samt forfarande for framstellning derav
GB1497039A (en)	1978-01-05	Penicillins and cephalosporins
GB1129158A (en)	1968-10-02	Coronary dilating compositions
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GB1332833A (en)	1973-10-03	Amindines
GB1440470A (en)	1976-06-23	Acylamino carboxylic acids and derivatives thereof
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