| Identification | Back Directory | [Name]
TERT-BUTYL 3-BENZYL-3,8-DIAZABICYCLO[3.2.1]OCTANE-8-CARBOXYLATE | [CAS]
149771-43-7 | [Synonyms]
3-Benzyl-8-Boc-3,8-diaza-bicyclo[3.2.1]octane
TERT-BUTYL 3-BENZYL-3,8-DIAZABICYCLO[3.2.1]OCTANE-8-CARBOXYLATE
3,8-Diazabicyclo[3.2.1]octane-8-carboxylic acid, 3-(phenylMethyl)-, 1,1-diMethylethyl ester | [Molecular Formula]
C18H26N2O2 | [MDL Number]
MFCD11973980 | [MOL File]
149771-43-7.mol | [Molecular Weight]
302.41 |
| Chemical Properties | Back Directory | [Boiling point ]
393.4±35.0 °C(Predicted) | [density ]
1.117±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,2-8°C | [pka]
8.57±0.20(Predicted) | [Appearance]
White to off-white Solid |
| Hazard Information | Back Directory | [Synthesis]
3-Benzyl-3,8-diazabicyclo[3.2.1]octane (13.5 g, 66.7 mmol) was used as starting material and mixed with triethylamine (6.75 g, 66.7 mmol) and di-tert-butyl dicarbonate (14.56 g, 66.7 mmol) in dichloromethane (100 ml). The reaction mixture was stirred under cooling in an ice bath for 3 hours. After completion of the reaction, the crude product was washed with water (150 ml) and the aqueous phase was then extracted with dichloromethane (50 ml). The organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give tert-butyl 3-benzyl-3,8-diazabicyclo[3.2.1]octane-8-carboxylate (13 g, 65% yield). The melting point of the product was 58-60°C. | [References]
[1] Journal of Medicinal Chemistry, 1998, vol. 41, # 5, p. 674 - 681
[2] Farmaco, 1993, vol. 48, # 3, p. 387 - 396
[3] Patent: EP1213289, 2002, A1. Location in patent: Page 12
[4] Patent: WO2006/106090, 2006, A1. Location in patent: Page/Page column 16
[5] Farmaco, 1998, vol. 53, # 8-9, p. 557 - 562 |
|
|