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CAS No. : | 1239319-91-5 | MDL No. : | MFCD18073249 |
Formula : | C12H21NO3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | KAVBYCOMZDNOFX-UHFFFAOYSA-N |
M.W : | 227.30 | Pubchem ID : | 69669842 |
Synonyms : |
|
Chemical Name : | tert-Butyl 2-hydroxy-6-azaspiro[3.4]octane-6-carboxylate |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-H315-H319-H332-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 |
---|---|---|
63% | With caesium carbonate; In N,N-dimethyl-formamide; at 20℃; for 16h; | A mixture of tert-butyl 2-hydroxy-6-azaspiro[3.4]octane-6-carboxylate 1 (950 mg, 4.18 mmol), <strong>[1196155-38-0]2-chloro-6-(trifluoromethyl)isonicotinonitrile</strong> 2 (1.03 g, 4.99 mmol), Cs2C03 (2.73 g, 8.4 mmol), and DMF (22 mL), was stirred at RT for 16 h. The mixture was partitioned between water, brine, aq. 1M HCI, and EtOAc. The organic layer was separated and the aq. layer re- extracted with additional EtOAc. The combined organic layers were dried (MgS04), filtered, and concentrated under reduced pressure. The residue was purified (silica gel; eluting 0-40percent EtOAc/hexanes) to afford compound 3 (1.04 g, 63percent) as a yellow oil. 1H NMR (300 MHz, DMSO-i): delta 8.00 (m, 1H), 7.77 (m, 1H), 5.14 (m, 1H), 3.10 - 3.30 (m, 6H), 2.00 - 2.20 (m, 2H), 1.80 - 2.00 (m, 2H), 1.36 (s, 9H); LCMS Mass: 342.0 (M++l - C4H9). |
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