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CAS No. : | 156478-71-6 | MDL No. : | MFCD02682402 |
Formula : | C11H20N2O4 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | WZBHMXRBXXCEDD-UHFFFAOYSA-N |
M.W : | 244.29 | Pubchem ID : | 2735642 |
Synonyms : |
|
Chemical Name : | 2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)acetic acid |
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 |
---|---|---|
With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; In dichloromethane; for 16h; | EDC (1.18g, 6.15 mmol) was added to a stirred solution of [N-BOC-PIPERAZINE] acetic acid [(L.] [OOG,] 4.10 mmol), 8-oxa-3-aza-bicyclo [3.2. 1. ] octane (0.556g, 4.92 mmol), 3-hydroxy benzotriazole (0.836g, 6.15 mmol), and diisopropylethylamine (2. 14ml, 12.31 mmol) in DCM (20 ml) at ambient temperature under nitrogen. After stirring for 16h the reaction was quenched by the addition of water [(20ML).] The phases were separated and the organics were washed with sat. brine [(20ML),] dried and evaporated to dryness under reduced pressure. The residue was purified by chromatography on silica, eluting with 0-10% MeOH/DCM to give 46 as a white solid (0.780g). MS-ESI: 340 (M++H). [1H NMR (CDC13)] 1.45 (s, 9H), 1.80-2. 00 (m, 4H), 2.30-2. 58 (m, 4H), 2.85-3. 04 (m, [2H),] 3.25 (d, 1H), 3.30-3. 57 (m, 3H), 3.78 (d, 1H), 4.12 (d, 1H), 4.36 (d, 3H). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; at 20℃; for 16h; | A mixture [OF N-BOC-4-PIPERAZINE-ACETIC] acid hydrochloride dihydrate (0.4g, 1.26 mmol), N- methyl-2-piperazinone (0.194g, [1.] [7MMOL),] DMAP [(L.] [OG,] 8.2 mmol) and EDC (0.4g, 2. [1MMOL)] in dichloromethane (60 ml) was stirred under a nitrogen atmosphere for 16h. The reaction mixture was washed with a [L.] OM aq. citric acid solution (2 x 50ml), sat. sodium bicarbonate solution, the organics separated, dried and evaporated to dryness under reduced pressure. The residue was purified by chromatography on silica eluting with 10- 20percent MEOH/EtOAc to give 66 (0.3g) as a solid foam. MS-ESI: 341 [(M++H).] [1H NMR (DMSOD6)] 1.50 (s, 9H), 2.48 (m, 4H), 2.97 (s, 3H), 3.22-3. 56 (m, 8H), 3.78 3.90 (2t, 2H), 4.09 4.29 (2s, 2H). |
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