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CAS No. : | 93-10-7 | MDL No. : | MFCD00006752 |
Formula : | C10H7NO2 | Boiling Point : | - |
Linear Structure Formula : | (C9H6N)COOH | InChI Key : | LOAUVZALPPNFOQ-UHFFFAOYSA-N |
M.W : | 173.17 | Pubchem ID : | 7124 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
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 triethylamine; In tetrahydrofuran; water; | EXAMPLE 55 Preparation of N-(1-carbamoyl-1,2-dimethylpropyl)quinaldamide STR203 To a solution of quinaldic acid (20 g, 0.116 mol) in tetrahydrofuran (500 ml) cooled to -9 C. is added methyl chloroformate (8.92 ml, 0.116 mol) followed by triethylamine (18.4 ml, 0.139 mol). After 20 minutes <strong>[40963-14-2]2-amino-2,3-dimethylbutyramide</strong> (15.1 g, 0.116 mol) is added and the mixture stirred overnight at room temperature. Water is added and the solution is reduced to 200 ml of a rotorvap. A white solid separates and is filtered off, water washed and dried. Recrystallization from absolute ethanol gives the product mp 179-180 C., 26.86 g (87%). Anal. calcd. for C16 H19 N3 O2: C, 67.34; H, 6.73; N, 14.72. Found: C, 67.14; H, 6.17; N, 14.72. |
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