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CAS No. : | 301673-16-5 | MDL No. : | MFCD04115304 |
Formula : | C10H20N2O3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 216.28 | Pubchem ID : | - |
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 |
---|---|---|
67.0% | With triethylamine; In tetrahydrofuran; at 10 - 30℃; for 1h; | To a solution of tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (1.00 g, 4.62 mmol) and triethylamine (0.967 ml, 6.94 mmol) in tetrahydrofuran (20 ml) was added 5-trifluoromethyl-2-fluorobenzoyl chloride (0.837 ml, 5.54 mmol) at room temperature, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give the object product (1.26 g, 67.0%) as an oil. 1H-NMR (CDCl3) δ; 1.47 (9H, s), 3.02 (3H, br s), 3.29 (1H, br s), 3.61 (1H, br s), 3.79 (1H, br s), 4.08-4.22 (2H, br s), 4.51-4.54 (1H, m), 4.85 (1H, br s), 7.21-7.26 (1H, m), 7.68-7.72 (2H, m) |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
50.3% | A mixture of <strong>[171178-50-0]2,6-difluoronicotinic acid</strong> (1.00 g, 6.28 mmol) and thionyl chloride (10 ml) was stirred at 85 C. for 2 hr, and the solvent was evaporated under reduced pressure. The residue was added to a solution of tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (1.00 g, 4.62 mmol) and triethylamine (1.29 ml, 9.24 mmol) in tetrahydrofuran (10 ml) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give the object product (830 mg, 50.3%) as a solid. 1H-NMR (CDCl3) δ; 1.47 (9H, s), 3.01 (3H, br s), 3.31-3.38 (1H, m), 3.61 (1H, br s), 3.78 (1H, br s), 4.12 (2H, br s), 4.45-4.48 (1H, m), 4.82 (1H, br s), 6.90-6.96 (1H, m), 7.94-8.06 (1H, m). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
83% | With sodium tetrahydroborate; ethanol; nickel dichloride; at 0℃; for 4h;Inert atmosphere; | To a mixture of 1-tert-butyl 3-methyl piperazine-1, 3-dicarboxylate (1.0 g, 4.1 mmol) , nickel chloride (640 mg, 4.9 mmol) and anhydrous ethanol (10 mL) was added sodium borohydride (380 mg, 10.0 mmol) at 0 . The mixture was stirred for 4 h and quenched with ice-water (5 mL) . The mixture was adjusted with concentrated hydrochloric acid to pH 1. After the mixture was clear, a NaOH aqueous solution (1.0 M) was added to adjust pH 10. The resulting mixture was extracted with EtOAc (10 mL × 3) . The combined organic layers were dried over anhydrous Na2SO4 and concentrated to give tert-butyl 3- (hydroxymethyl) piperazine-1-carboxylate as a reseda solid (890 mg, 83) .1H NMR (400 MHz, CD3OD) : delta ppm 3.99-4.02 (m, 1H) , 3.90-3.93 (m, 1H) , 3.48-3.54 (m, 2H) , 2.96-3.00 (m, 1H) , 2.83-2.93 (m, 1H) , 2.66-2.72 (m, 2H) , 2.56-2.66 (m, 1H) , 1.48 (m, 9H) and MS-ESI: m/z 217.10 [M+H] +. |
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