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CAS No. : | 86-59-9 | MDL No. : | MFCD00047619 |
Formula : | C10H7NO2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | QRDZFPUVLYEQTA-UHFFFAOYSA-N |
M.W : | 173.17 | Pubchem ID : | 66582 |
Synonyms : |
|
Chemical Name : | Quinoline-8-carboxylic acid |
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With trifluoroacetic acid; In water; N,N-dimethyl-formamide; | Using the method of Example 12 the following compounds of the invention are prepared from the starting quinolines listed in the table. example 11 to a solution of 1.7 g. (10 mmole) of 8-quinoline carboxylic acid in 50 ml. of N,N-dimethylformamide is added 1.6 g. (10 mmole) of carbonyl diimidazole, and the mixture is stirred for four hours at 100 C. The reactive intermediate which is formed is reacted with 1.0 g. (10 mmole) of 5-amino-2-methyltetrazole. The reaction is carried out by adding the solution and two drops of trifluoroacetic acid to the stirred solution of reactive intermediate and heating for four hours at 140-150 C. The solution is then evaporated to remove the N,N-dimethylformamide. Water is added to the residue, the mixture is cooled, then filtered. The solid product is recrystallized from ethanol to provide 8-(2-methyl-1H-tetrazol-5-ylcarbamoyl)quinoline, m.p. 222-223 C. |
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