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CAS No. : | 65169-43-9 | MDL No. : | MFCD07375372 |
Formula : | C8H8ClNO2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | FOKUGIKLNXFRTI-UHFFFAOYSA-N |
M.W : | 185.61 | Pubchem ID : | 11636946 |
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 |
---|---|---|
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; In toluene; for 5.5h;Reflux; Inert atmosphere; | [Example 124] (1087) (1088) The mixture of 118 mg of <strong>[26807-73-8]1-benzyl-1H-indol-5-amine</strong>, 100 mg of methyl 2-chloro-5-methylnicotinate, 25 mg of tris(dibenzylideneacetone)dipalladium(0), 31 mg of 4,5'-bis(diphenylphosphino)-9,9'-dimethylxanthene, 352 mg of cesium carbonate, and 5 mL of toluene, was heated at reflux for five hours and 30 minutes under a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and ethyl acetate and water were then added thereto. The organic layer was separated, washed with a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (gradient elution with hexane:ethyl acetate = 100:0-70:30). Water and methanol were added to the thus obtained residue, and the solid was collected by filtration to give 60 mg of methyl 2-((1-benzyl-1H-indol-5-yl)amino)-5-methylnicotinate as a yellow solid. 1H-NMR (DMSO-d6) delta: 2.27 (3H, s), 3.88 (3H, s), 5.40 (2H, s), 6.44 (1H, d, J = 2.6 Hz), 7.14-7.39 (7H, m), 7.48 (1H, d, J = 2.6 Hz), 7.95 (1H, d, J = 1.3 Hz), 8.05 (1H, d, J = 2.0 Hz), 8.21 (1H, d, J = 2.0 Hz), 9.82 (1H, s). MS (ESI, m/z): 372 (M+H)+. |
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