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CAS No. : | 108612-54-0 | MDL No. : | MFCD02683051 |
Formula : | C11H22N2O2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | DJJOYDXRUBOZON-UHFFFAOYSA-N |
M.W : | 214.30 | Pubchem ID : | 2756806 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | 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 |
---|---|---|
65% | With potassium carbonate; In dimethyl sulfoxide; at 120℃; for 48h; | Preparation 1 tert-Butyl l-(6-chloro-4,5-dimethylpyridazin-3-yl)piperidin-4-yl(methyl)carbamate; Heat a mixture of <strong>[34584-69-5]3,6-dichloro-4,5-dimethylpyridazine</strong> (11.0 g, 62.1 mmol), tert- butyl methyl(piperidin-4-yl)carbamate (23.3 g, 109 mmol), and powdered K2CO3 (17.2 g, 124 mmol) in DMSO (310 mL) at 120 0C for 2 d. Cool the reaction mixture, dilute with H2O, and filter off the solid. Rinse the solid with H2O, and dry under vacuum at 45 0C. Dissolve the solid in CH2CI2, and pass the solution through a pad of silica gel, eluting with CH2CI2. Concentrate the organic layer under reduced pressure to obtain the title compound as a yellow solid (14.3 g, 65%). ES/MS m/z (35Cl) 355.0 (M+l). |
30% | With N-ethyl-N,N-diisopropylamine; In 1-methyl-pyrrolidin-2-one; at 150℃; for 5h; | tert-Butyl piperidin-4-ylmethylcarbamate (3.8i g, i 7.8mmol), <strong>[34584-69-5]3,6-dichloro-4,5-dimethyl-pyridazine</strong> (3.Og, i7.Ommol), NMP (i4mL) and N,N-Diisopropylethylamine (4.43mL, 25.4mmol) were added to a round bottom flask and heated to iSO C for 5 h. The mixture was partitioned between EtOAc (i 00 mL) and i M Na2003 aq. (50 mL). The organic layer was washed with i M Na2003 aq. (5OmL),water (2 x 7OmL), brine (70 mL), before passage through a hydrophobic frit and concentrated in vacuo to give an orange/brown solid. The crude material was purified by silica flash chromatography using 0% EtOAc in heptane with tn ethylamine i% with a gradient increasing to 30% ethyl actetate. Fractions containing product were combined and concentrated in vacuo to afford tert-butyl N-[i -(6-chloro-4,5-dimethyl-pyridazin-3-yl)-4-piperidyl]-N-methyl-carbamate(i .8g,5.i mmol, 30% yield).1H NMR (400MHz, ODd3) s/ppm: 4.34-3.84 (m, 2H), 3.56-3.47 (m(br), 2H), 3.00 (t(br), Ji2.OHz,2H), 2.78 (s, 3H), 2.3i (s, 3H), 2.25 (s, 3H), i .93-i .80 (m, 2H), i .78-i .7i (m(br), 2H), i .47 (s, 9H).MS Method 2: RT: i .88 mi m/z 355.9 [M÷H]÷ |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
56% | With sodium cyanoborohydride; acetic acid; In methanol; at 20℃; for 16h; | 4-Bromopicolinaldehyde (500 mg, 2.69 mmol) and ierf-butyl methyl(piperidin-4- yl)carbamate (634 mg, 2.96 mmol) were dissolved in 50 mL methanol. Sodium cyanoborohydride (254 mg, 4.04 mmol) and four drops of acetic acid were added and the reaction mixture was stirred at room temperature for 16 h. The solvent was evaporated and the crude was re-dissolved in dichloromethane, washed with sodium carbonate and sodium hydroxide. The organics were dried over sodium sulphate, filtered and concentrated under reduced pressure. The yellow oil obtained was purified by reverse phase using SP1? Purification System to give 573 mg (56percent yield) of the title compound. LRMS (m/z): 385 (M+1 )+. |
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