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CAS No. : | 1124382-72-4 | MDL No. : | MFCD16658939 |
Formula : | C6H5BrN4 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | SUFKKFLJJMKVJJ-UHFFFAOYSA-N |
M.W : | 213.04 | Pubchem ID : | 46864069 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-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 |
---|---|---|
81% | With tetrakis(triphenylphosphine) palladium(0); sodium carbonate; In ethanol; water; toluene; at 120℃; for 8h; | General procedure: 8-Bromo- [1,2,4] triazolo [1,5-a] pyridin-2-amine 10 g (46.9 mmol) and 9-phenyl-3- (4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl) to -9H-carbazole 19.1 g (51.6 mmol) was added to 200 mL toluene, 50 mL EtOH, 50 mL H2O. Pd(PPh3)4 2.7 g (2.3 mmol), Na2CO3 14.9 g (141 mmol) was added at 8 hours after 120 was heated to reflux. It was cooled to room temperature and stop the reaction with 300 mL of purified water to the reaction solution. Extract the mixture with E.A 500 mL, and washed with distilled water. The resulting organic layer was dried over anhydrous MgSO4, was evaporated under reduced pressure, and purified by silica gel column chromatography to give the title compound 13.0 g (yield 74%).Reaction with Preparation Example 1 and 4 - (naphthalen-1-yl) phenylboronic acid with the exception of that, the Preparation Example 2 and the same procedure carried out by the desired compound 12.8 g (yield 81%) was obtained. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
87% | With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; caesium carbonate; In 1,4-dioxane; water; at 100℃; | a) 8-(4-(Trifluoromethylthio)phenyl)-ri,2,41triazolori,5-alpyridin-2-amine In a 150 ml round-bottomed flask, 8-bromo-[l,2,4]triazolo[l,5-a]pyridin-2-amine (1.40 g, 6.58 mmol), 4,4,5,5-tetramethyl-2-(4-(trifluoromethylthio)phenyl)-l,3,2-dioxaborolane (2.00 g, 6.58 mmol) and cesium carbonate (4.29 g, 13.2 mmol) were combined with dioxane (80 ml) and water (8.00 ml) to give a white suspension. l,l'-Bis(diphenylphosphino)ferrocene- palladium(II)dichloride dichloromethane complex (481 mg, 658 μπιο) was added. The reaction mixture was heated to 100C and stirred overnight. Chromatography (silica gel, 70 g, ethyl acetate/heptane = 30:70 to 100:0) yielded the title compound as a light brown solid (1.77 g, 87%). MS: m/z = 311.0 [M+H]+. |
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