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CAS No. : | 406235-30-1 | MDL No. : | MFCD04972471 |
Formula : | C11H21NO3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | SWUCHJAQBNXPBO-UHFFFAOYSA-N |
M.W : | 215.29 | Pubchem ID : | 22730812 |
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 |
---|---|---|
Preparation of tert-butyl 4-(pyridazin-3-yloxy)piperidine-l-carboxylate. To a solution of tert-butyl 4-hydroxy-4-methylpiperidine-l-carboxylate (140 mg, 0.696 mmol) in DMF (2.3 mL) was added sodium hydride (60percent w/w, 56 mg, 1.39 mmol). The reaction was stirred for 10 min at ambient temperature. Then <strong>[1120-95-2]3-<strong>[1120-95-2]chloropyridazine</strong></strong> (159 mg, 1.39 mmol) was added and reaction stirred 3 h at 95°C. The reaction was cooled to ambient temperature and diluted with water and extracted with EtOAc. Combined organics were washed with saturated NaHC03(aq), water, and brine. The combined organic extracts were dried over anhydrous Na2S04(S), filtered and concentrated in vacuo to afford the title compound (assumed quantative yield, 194 mg) in sufficient purity for step 2. MS (apci) m/z = 280.2 (M+H). |
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