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CAS No. : | 138775-03-8 | MDL No. : | MFCD02179111 |
Formula : | C18H24N2O6 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | SREPAMKILVVDSP-AWEZNQCLSA-N |
M.W : | 364.39 | Pubchem ID : | 7010652 |
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 |
---|---|---|
Step 1 :(S)-4-(Benzyloxycarbonyl)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid (1.00 g, 2.70 mmol), HOBt (520 mg, 3.80 mmol), HBTU (1.35 g, 3.60 mmol) and DIPEA (955 uL, 5.50 mmol) were dissolved in dry DMF (10 ml) under N2 and stirred for 10 minutes at room temperature. R-1,2,3,4-Tetrahydro-1-naphtylamine (485 mg, 3.30 mmol) was added and <n="83"/>the solution was left to stir for 18 hours at room temperature. The contents were then added to a separatory funnel along with EtOAc and washed with 10% citric acid, saturated NaHCO3 and brine. The organic layer was collected, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to provide intermediate 5-a as a white solid. |
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