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CAS No. : | 40472-88-6 | MDL No. : | MFCD16988536 |
Formula : | C8H10BrNO | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 216.08 | Pubchem ID : | - |
Synonyms : |
|
Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501 | UN#: | 2810 |
Hazard Statements: | H301-H311-H331 | Packing Group: | Ⅲ |
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); sodium t-butanolate; tert-butyl XPhos; In toluene; at 80℃; for 14h;Sealed tube; Microwave irradiation; | To a solution of 4-fluro-1H-indazole (11.3 mg, 0.083mmol) in toluene (1 mL) in a microwave vial were added 2-(5-bromo-3-pyridinyl)-2-propanol (18 mg, 0.083 mmol), tris(dibenzylideneacetone) palladium (0) (7.6 mg, 8.33 umol), sodium tert-butoxide (12 mg, 0.125 mmol) and 2-di-tert-butylphosphino-2',4',6'- triisopropylbiphenyl (3.5 mg, 8.33 umol). The resulting mixture was sealed and heated to 80 C for 14 hours, then concentrated under reduced pressure. Purification by flash chromatography on silica gel (0% to 50% ethyl acetate/hexanes linear gradient) provided the title compound: LCMS m/z 271.98 [M + H]+; 1H NMR (500 MHz, CD3OD) delta 8.74 - 8.75 (m, 2 H), 8.40 (d, J= 2.4 Hz, 1 H), 8.20 (d, J= 2.7 Hz, 1 H), 7.71 (ddd, J= 4.0, 10.8, 12.8 Hz, 1 H), 7.22 - 7.30 (m, 3 H), 1.65 (s, 6 H). | |
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; tert-butyl XPhos; In toluene; at 80℃; for 14h;Microwave irradiation; Sealed tube; | To a solution of <strong>[341-23-1]4-fluoro-1H-indazole</strong> (11.3 mg, 0.083 mmol) in toluene (1 mL) in a microwave vial were added 2-(5-bromo-3-pyridinyl)-2-propanol (18 mg, 0.083 mmol), tris(dibenzylideneacetone) palladium (0) (7.6 mg, 8.33 umol), sodium tert-butoxide (12 mg, 0.125 mmol) and 2-di-tert-butylphosphino-2',4'6'-triisopropylbiphenyl (3.5 mg, 8.33 umol). The resulting mixture was sealed and heated to 80 C for 14 hours, then concentrated under reduced pressure. Purification by flash chromatography on silica gel (0% to 50% ethyl acetate/hexanes linear gradient) provided the title compound: HRMS (Positive ESI) m/z 272.1199 (272.1199 calcd for C15H14FN3O); 1H NMR (500 MHz, CD3OD) d 8.74 - 8.75 (m, 2 H), 8.40 (d, J = 2.4 Hz, 1 H), 8.20 (d, J = 2.7 Hz, 1 H), 7.71 (ddd, J = 4.0, 10.8, 12.8 Hz, 1 H), 7.22 - 7.30 (m, 3 H), 1.65 (s, 6 H). |
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