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CAS No. : | 196613-57-7 | MDL No. : | MFCD07371372 |
Formula : | C11H22N2O2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | YCOKHOLOSGJEGL-UHFFFAOYSA-N |
M.W : | 214.30 | Pubchem ID : | 18946151 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-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 isopropyl alcohol; at 90℃; for 0.5h;Microwave irradiation; | Preparation 30 A mixture of <strong>[154012-15-4]ethyl 4,6-dichloro-5-nitronicotinate</strong> (3.05 g), racemic tert-butyl 4-aminoazepan-1-caboxylate (2.47 g), DIPEA (4 mL) and i-PrOH (7.625 mL) was stirred at 90C for 30 minutes under microwave irradiation. The reaction mixture was cooled to ambient temperature. The mixture was diluted with EtOAc (20 mL), and water (20 mL) was added. The organic layer was extracted, washed with brine, dried over anhydrous MgSO4, filtered. The filtrate was evaporated in vacuo. The residue was purified by silica gel column chromatography (EtOAc: n-hexane) to afford racemic tert-butyl 4-[2-chloro-5-(ethoxycarbonyl)-3-nitropyridine-4-yl]amino}azepan-1-carboxylate (3.43 g) as a yellow solid. |
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