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| | 1-Boc-4-Propylaminopiperidine Basic information |
| Product Name: | 1-Boc-4-Propylaminopiperidine | | Synonyms: | 4-PROPYLAMINO-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;4-PROPYLAMINO-1-BOC-PIPERIDINE;4-Propylamino-1-Boc;1-BOC-4-PROPYLAMINOPIPERIDINE;tert-butyl 4-(propylamino)piperidine-1-carboxylate;N-Boc-4-propylaminopiperidine;4-(Prop-1-ylamino)piperidine, N1-BOC protected 97%;1-Piperidinecarboxylic acid, 4-(propylamino)-, 1,1-dimethylethyl ester | | CAS: | 301225-58-1 | | MF: | C13H26N2O2 | | MW: | 242.36 | | EINECS: | | | Product Categories: | | | Mol File: | 301225-58-1.mol |  |
| | 1-Boc-4-Propylaminopiperidine Chemical Properties |
| Boiling point | 322.6±35.0 °C(Predicted) | | density | 0.99±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | pka | 10.25±0.20(Predicted) |
| | 1-Boc-4-Propylaminopiperidine Usage And Synthesis |
| Synthesis | Step A: N-tert-butoxycarbonyl-4-piperidone (5 g, 25 mmol), n-propylamine (3.69 mL, 45 mmol), acetic acid (1.43 mL, 25 mmol), and sodium triacetoxyborohydride (7.95 g, 37.5 mmol) were dissolved in dichloromethane (100 mL) and the reaction was stirred for 16 h at room temperature. After completion of the reaction, the reaction mixture was washed with deionized water (50 mL) and then with saturated sodium bicarbonate solution. The aqueous phase was back-extracted with dichloromethane (20 mL), and all organic phases were combined, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure to give 1-N-Boc-4-propylaminopiperidine 6 g in 95% yield. | | References | [1] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 18, p. 2475 - 2479
[2] Patent: US6498161, 2002, B1
[3] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 1, p. 336 - 343 |
| | 1-Boc-4-Propylaminopiperidine Preparation Products And Raw materials |
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