GB1527110A - 2-thienylsulphinylacetic acid - Google Patents
2-thienylsulphinylacetic acidInfo
- Publication number
- GB1527110A GB1527110A GB1649478A GB1649478A GB1527110A GB 1527110 A GB1527110 A GB 1527110A GB 1649478 A GB1649478 A GB 1649478A GB 1649478 A GB1649478 A GB 1649478A GB 1527110 A GB1527110 A GB 1527110A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- thienylsulphinylacetic
- isomer
- dec
- thienylthioacetic
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/34—Sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
1527110 2-Thienylsulphinylacetic acid ASAHI KASEI KOGYO KK 22 Dec 1975 [28 Dec 1974 15 July 1975] 16494/78 Divided out of 1527109 Heading C2C 2-Thienylsulphinylacetic acid is obtained by oxidation of 2-thienylthioacetic acid with H 2 O. The starting material may be obtained from 2- mercaptothiophene and monochloroacetic acid. The isomer having positive optical rotation (α) D in ethanol is useful in the preparation of cephalosporin derivatives having lower minimum inhibiting concentration against Gramnegative bacteria c. f. the isomer with negative rotation.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14918074A JPS5180886A (en) | 1974-12-28 | 1974-12-28 | GANIOSEFUAROSUHORINNOSEIHO |
JP8576375A JPS5210289A (en) | 1975-07-15 | 1975-07-15 | Process for preparing penicillins and cephalosporins having thionylsul finyl group |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1527110A true GB1527110A (en) | 1978-10-04 |
Family
ID=26426769
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1649478A Expired GB1527110A (en) | 1974-12-28 | 1975-12-22 | 2-thienylsulphinylacetic acid |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1527110A (en) |
-
1975
- 1975-12-22 GB GB1649478A patent/GB1527110A/en not_active Expired
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19921222 |