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CAS No. : | 162046-66-4 | MDL No. : | MFCD04115067 |
Formula : | C16H22N2O4 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | BEDWYXZFIYMEJG-UHFFFAOYSA-N |
M.W : | 306.36 | Pubchem ID : | 2795508 |
Synonyms : |
|
Chemical Name : | 4-(4-(tert-Butoxycarbonyl)piperazin-1-yl)benzoic acid |
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 |
---|---|---|
35% | With dmap; In dichloromethane; at 20℃; | Example 163 4-[4-(3-tert-Butyl-phenylcarbamoyl)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester A mixture of 3-tert-butyl aniline (117 mg, 0.78 mmol), 4-(4-carboxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (prepared as described in ) (200 mg, 0.65 mmol), EDCI (375 mg, 0.95 mmol) and a catalytic amount of DMAP in CH2Cl2 was stirred at room temperature overnight. The next day the mixture was partitioned between EtOAc and water. The organic layer was collected, dried over Na2SO4, filtered and concentrated. The residue was chromatographed with silica gel column amd 0-30percent EtOAc in hexanes gradient to afford the product (100 mg, Yield: 35percent). HRMS m/z calcd for C26H35N3O3 [M+H]+: 438.2751; Found: 438.2753. |
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