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CAS No. : | 111196-81-7 | MDL No. : | MFCD00799503 |
Formula : | C6H7ClN2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | BGLLZQRUXJGTAD-UHFFFAOYSA-N |
M.W : | 142.59 | Pubchem ID : | 3572763 |
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 |
---|---|---|
75% | With potassium carbonate; In N,N-dimethyl-formamide; at 65℃; for 12h; | (Step 6-3) Preparation of 3-(l -(5-ethylpyrimidin-2-yl)piperidin-4-yl)propan-l-ol 2-chloro-5-ethyl pyrimidine (1.0 g, 7.0 mmol) was dissolved in N,N-dimethyl formamide (DMF, 15 ml), and then 3-(piperidin-4-yl)propan-l -ol (1.1 g, 7.7 mmol) and potassium carbonate (K2C03, 2.9 g, 21.0 mmol) were added to the reaction solution. The reaction solution was stirred at 65 °C for 12 hours, and then diluted with water, and extracted with EA. Moisture was removed from an organic layer with MgSC^, the organic layer was filtered and concentrated under reduced pressure, and the residue was purified with silica gel column chromatography to obtain the desired form of the compound, 3-(l-(5-ethylpyrimidin-2-yl)piperidin-4-yl)propan-l -ol in a yield of 75percent. H MR(400MHz, CDC13) delta 8.15 (; s, 2H), 4.67 (d, 2H, J=13.6Hz), 2.87 (m, 2H), 2.83 (t, 2H, J=12.6 Hz), 2.44 (q, 2H, J=7.6Hz), 1.46-1.38 (m, 9H), 1.21 (t, 3H, J=7.6Hz) |
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