CAS No. : | 54745-74-3 | MDL No. : | MFCD09800611 |
Formula : | C6H12ClNO | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | XADOTNAXKKFKDY-UHFFFAOYSA-N |
M.W : | 149.62 | Pubchem ID : | 21983536 |
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 |
---|---|---|
With N-ethyl-N,N-diisopropylamine; In ethanol; N,N-dimethyl-formamide; at 45.0℃; for 65.0h;Inert atmosphere; | Step 1-A 20 mL vial equipped with a stirring bar and a Teflon cap was charged with 8-oxa-3azabicyclo[3.2.1]octane hydrochloride (101 mg, 0.673 mmol) followed by p (112 mg, 0.511 mmol). The solids were dissolved in anhydrous ethanol/DMF and heated gently with a heating gun to effect dissolution. After cooling to room temperature, N,N diisopropylethylamine (0.5 mL, 2.56 mmol) was added via syringe, the vial flushed with nitrogen, capeed and placed in a pre heated 45 C. heating block. After heating for 65 h at 45 an aliquot was removed and the progress of the reaction determined by LC-MS. Compound (p) was completely consumed and the reaction worked up as described in Example 105 to afford 156 mg of crude compound (gx) as an off white solid. LC-MS and NMR indicated the crude product was of high purity and could be used directly in the next step: (gx)1H NMR (400 MHz, DMSO) delta 5.10 (s, 2H), 4.38 (br d, J=1.7 Hz, 2H), 3.73 (br s, 1H), 3.32 (s, 1H), 3.20 (d, J=12.2 Hz, 2H), 2.70 (dd, J=41.2, 15.4 Hz, 1H), 2.01-1.51 (m, 4H), 1.32 (s, 6H). LC-MS: m/z=+296.3(M+H)+. |
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