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CAS No. : | 734524-15-3 | MDL No. : | MFCD09787869 |
Formula : | C10H6FNO2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | PXJCGANFXZBADU-UHFFFAOYSA-N |
M.W : | 191.16 | Pubchem ID : | 17040038 |
Synonyms : |
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Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-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 |
---|---|---|
16% |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With N-ethyl-N,N-diisopropylamine; HATU In 1,2-dichloro-ethane at 60℃; for 12h; | 94.4 Step 4. Into a 25-mL round-bottom flask was placed 7-fluoroquinoline-3-carboxylic acid (100 mg, 0.52 mmol), DCE (4 mL), 3-(2-amino-5-chloro-4-methoxyphenyl)-4,5-dihydro-1,2,4-oxadiazol-5-one (138.8 mg, 0.57 mmol), HATU (258.6 mg, 0.68 mmol) and DIEA (202.6 mg, 1.57 mmol). The resulting solution was stirred for 12 hrs at 60 °C in an oil bath. The resulting mixture was concentrated under vacuum and washed with 10 mL of methanol. The solids were collected by filtration to afford the title compound as a light yellow solid. LC-MS 415 (M+H)+. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With N-ethyl-N,N-diisopropylamine; HATU In 1,2-dichloro-ethane at 60℃; for 12h; | 121.3 Step 3: N-(4-bromo-2-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)phenyl)-7-fluoroquinoline-3-carboxamide. Into a 25-mL round-bottom flask was placed 7-fluoroquinoline- 3-carboxylic acid (200 mg, 1.05 mmol), DCE (10 mL), 3-(2-amino-5-bromophenyl)-4,5-dihydro-1,2,4-oxadiazol-5-one (293.7 mg, 1.15 mmol), HATU (596.9 mg, 1.57 mmol), DIEA (405.2 mg, 3.14 mmol). The resulting solution was stirred for 12 hrs at 60 °C in an oil bath. The resulting solution was diluted with 10 mL of methanol. The solids were collected by filtration. This resulted in 290 mg (crude) of N-[4-bromo-2-(5-oxo-4,5-dihydro-l,2,4-oxadiazol-3-yl)phenyl]-7-fluoroquinoline-3-carboxamide as a yellow solid. |
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