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CAS No. : | 160357-94-8 | MDL No. : | MFCD03412449 |
Formula : | C7H14N2O | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | NLHBHVGPMMXWIM-UHFFFAOYSA-N |
M.W : | 142.20 | Pubchem ID : | 4962477 |
Synonyms : |
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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 |
---|---|---|
10% | With hydrogen In ethanol for 16 h; | Example 307; 1 -(4-Amino-piperidin-1 -vl)-ethanone:; 1-Acetyl-piperidin-4-one (10 gm (70 mmol)) was dissolved in 200 ml ethanol and treated with 10 gm (143 mmol) hydroxylamine hydrochloride and 10 ml pyridine. The reaction mixture was heated to 70 °Cfor 1.5 hr. The solvent was removed and the residue was treated with water and cooled to 0 °C. The resulting slurry was filtered and dried under vacuum to afford 6.5 gm 1-Acetyl-piperidin-4-one oxime as a white solid (59 percent). The oxime (2.0 gm (12 mmol)) in a Parr bottle was dissolved in 50 ml of ethanol and treated with 0.2 gm of Raney nickel which had been washed several times with water. The reaction was placed in to Parr apparatus and hydrogenated under 50 psi hydrogen pressure for 16 hours. The mixture was carefully filtered and the filtrate was evaporated in vacuo to afford 1.7 gm (100 percent) of the desired amine as a green solid. GC Mass spectrum m/z =142 |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
2.2 g | With hydrogenchloride In 1,4-dioxane at 20℃; for 5 h; | To a stirred suspension of ie f-butyl (1 -acetylpiperidin-4-yl) carbamate (6.61 g, 27.310 mmol) in dioxane (10 ml) was added 2.5 N HCI in dioxane (20 ml) at room temperature and the resulting reaction mixture was stirred at room temperature for 5 h. The resulting reaction mixture was concentrated under reduced pressure yielding 1 -(4-aminopiperidin-1 -yl) ethanone (2.20 g, 15.490 mmol) which was used in the next step without further purification. LCMS: Method B, 0.624 min, MS: ES+ 143.4 (M+1 ). |
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