GB619087A - Improvements in or relating to the decarboxylation of 1:3-dialkyl-pyridofluorenone-4-carboxylic acids - Google Patents
Improvements in or relating to the decarboxylation of 1:3-dialkyl-pyridofluorenone-4-carboxylic acidsInfo
- Publication number
- GB619087A GB619087A GB3416246A GB3416246A GB619087A GB 619087 A GB619087 A GB 619087A GB 3416246 A GB3416246 A GB 3416246A GB 3416246 A GB3416246 A GB 3416246A GB 619087 A GB619087 A GB 619087A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pyridofluorenone
- acid
- dialkyl
- decarboxylation
- pyridofluorenones
- 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
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/16—Ring systems of three rings containing carbocyclic rings other than six-membered
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,3-Dialkyl-pyridofluorenones in which the alkyl groups do not contain more than six carbon atoms are obtained by heating the correspondingly substituted pyridofluorenone-4-carboxylic acid in an inert organic liquid at a temperature of 250-320 DEG C. to effect decarboxylation. Liquids specified are aliphatic or aromatic high boiling hydroxylic compounds, esters, bases or hydrocarbons such as liquid paraffin, glycerol and butyl phthalate. 300-320 DEG C. is the preferred temperature range. Acid salts of the pyridofluorenones are obtained on treatment with acid the isethionates being preferred. In examples: (1) 1,3-dimethyl-pyridofluorenone is obtained by heating 1,3-dimethyl-pyridofluorenone-4-carboxylic acid in liquid paraffin, and (2) the isethionate thereof obtained by treatment with isethionic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3416246A GB619087A (en) | 1946-11-18 | 1946-11-18 | Improvements in or relating to the decarboxylation of 1:3-dialkyl-pyridofluorenone-4-carboxylic acids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3416246A GB619087A (en) | 1946-11-18 | 1946-11-18 | Improvements in or relating to the decarboxylation of 1:3-dialkyl-pyridofluorenone-4-carboxylic acids |
Publications (1)
Publication Number | Publication Date |
---|---|
GB619087A true GB619087A (en) | 1949-03-03 |
Family
ID=10362163
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3416246A Expired GB619087A (en) | 1946-11-18 | 1946-11-18 | Improvements in or relating to the decarboxylation of 1:3-dialkyl-pyridofluorenone-4-carboxylic acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB619087A (en) |
-
1946
- 1946-11-18 GB GB3416246A patent/GB619087A/en not_active Expired
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