GB1024645A - Chromone compounds - Google Patents
Chromone compoundsInfo
- Publication number
- GB1024645A GB1024645A GB2640362A GB2640362A GB1024645A GB 1024645 A GB1024645 A GB 1024645A GB 2640362 A GB2640362 A GB 2640362A GB 2640362 A GB2640362 A GB 2640362A GB 1024645 A GB1024645 A GB 1024645A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chroman
- hydroxy
- acid
- contacting
- propionic 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
The invention comprises 6-oxa-cyclohexano-[g] - chromone - 2 - carboxylic acid, salts and esters thereof and a process for the preparation thereof by condensing 7-acetyl-6-hydroxy-chroman with ethyl oxalate and cyclising the resultant diketone by heating with ethanolic HCl, H2SO4 or boron trifluoride to obtain the ethyl ester, or with glacial acetic acid and HCl to obtain the free acid. The 7-acetyl-6-hydroxy-chroman may be obtained by contacting b -(p-methoxyphenoxy) propionic acid with a strong acid catalyst to yield 6-methoxy-chromanone, reducing the chromanone to 6-methoxy chroman and contacting this with boron trifluoride acetic acid complex, or by acetylating b -(p-hydroxy-phenoxy) propionic acid with acetic anhydride, contacting the resulting (p-acetoxyphenoxy) propionic acid with a strong acid catalyst to yield 6-hydroxy chroman, acetylating to form 6-acetoxy chroman which is contacted with aluminium chloride. Pharmaceutical compositions having activity as inhibitors of the antigen-antibody reaction and containing the above compounds are administered orally in tablets, in solutions for injection or topically as creams, lotions and pastes or in an aerosol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2640362A GB1024645A (en) | 1962-07-10 | 1962-07-10 | Chromone compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2640362A GB1024645A (en) | 1962-07-10 | 1962-07-10 | Chromone compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1024645A true GB1024645A (en) | 1966-03-30 |
Family
ID=10243098
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2640362A Expired GB1024645A (en) | 1962-07-10 | 1962-07-10 | Chromone compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1024645A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4238606A (en) * | 1974-11-30 | 1980-12-09 | Fisons Limited | Tricyclic mono-chromone-2-carboxylic acids |
-
1962
- 1962-07-10 GB GB2640362A patent/GB1024645A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4238606A (en) * | 1974-11-30 | 1980-12-09 | Fisons Limited | Tricyclic mono-chromone-2-carboxylic acids |
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