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CAS No. : | 1137826-05-1 | MDL No. : | MFCD18417138 |
Formula : | C10H7NO3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | OKIIDYYKVMNMGL-UHFFFAOYSA-N |
M.W : | 189.17 | Pubchem ID : | 58902455 |
Synonyms : |
|
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 |
---|---|---|
91% | With hydrogen bromide; acetic acid In water at 140℃; for 1 h; Microwave irradiation | Example 11: N-hydroxy-6-phenoxyquinoline-3-carboxamide Compound 1-12 Step 1: 6-hydi*oxyquinoline-3-carboxylic acid Intermediate-15 [00183] 6-Methoxyquinoline-3-carbox lic acid (0.75 g, 3.69 mmol) was placed in a 20 mL microwave vial fitted with a stirbar. The solid was suspended in acetic acid (7 mL) and hydrobrorrric acid (48 percent in water, 3.5 mL) was added. The vial was capped and the suspension was carefully heated under microwave irradiation at 140 °C for 1 h. After reaction, the vial was thoroughly cooled to room temperature and very carefully vented with an 18 g needle in a fume hood prior to opening. The solids were collected by filtration and washed with ethyl acetate to afford the title product as a solid (0.678 g, 91 percent). LC-MS: (FA) ES+ 190; .H NMR (400 MHz, d6-DMSO) δ ppm 10.68 (br s, 1 H), 9.26 (d, J = 1.9 Hz, 1 H), 9.14 (d, J = 1.3 Hz, 1 H), 8.08 (d, J = 9.1 Hz, 1 H), 7,62 (dd, J = 9.1, 2.7 Hz, 1 H), 7.52 (d, J = 2.7 Hz, 1 H). |
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