1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98
1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98 Basic information
- Product Name:
- 1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98
- Synonyms:
-
- 1-Benzyl-4-(N-Boc-amino)piperidine
- (1-Benzyl-piperidin-4-yl)-carbamic acid tert-butyl ester
- tert-butyl N-(1-benzylpiperidin-4-yl)carbamate
- 4-Boc-aMino-1-benzylpiperidine
- N-Benzyl-4-(N-Boc-aMino)piperidine
- tert-Butyl 1-benzylpiperidin-4-ylcarbamate
- 4-(N-Boc-aMino)-1-benzyl-piperidine
- 1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98
- CAS:
- 73889-19-7
- MF:
- C17H26N2O2
- MW:
- 290.4
- Product Categories:
-
- Building Blocks
- Heterocyclic Building Blocks
- Piperidines
- Amines and Anilines
- Heterocycles
- Mol File:
- 73889-19-7.mol
1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98 Chemical Properties
- Melting point:
- 122-125 °C(lit.)
- Boiling point:
- 400.9±34.0 °C(Predicted)
- Density
- 1.07±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 12.35±0.20(Predicted)
- Appearance
- White to off-white Solid
1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98 Usage And Synthesis
Chemical Properties
White powder
Synthesis
50541-93-0
24424-99-5
73889-19-7
General procedure for the synthesis of tert-butyl (1-benzylpiperidin-4-yl)carbamate from 4-amino-1-benzylpiperidine and di-tert-butyl dicarbonate: to an anhydrous solution of 4-amino-1-benzylpiperidine (1 mL, 933 mg, 4.9 mmol) in dichloromethane (20 mL) was added triethylamine (1 mL, 725 mg, 7.2 mmol) and di-tert-butyl dicarbonate ( 1.23 g, 5.6 mmol). The reaction mixture was stirred overnight at room temperature and then diluted with dichloromethane (20 mL). The organic layer was washed sequentially with saturated aqueous sodium bicarbonate (10 mL) and saturated saline (10 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give tert-butyl (1-benzylpiperidin-4-yl)carbamate (1.42 g, quantitative yield) as a white solid.
References
[1] Patent: WO2013/140148, 2013, A1. Location in patent: Page/Page column 65
[2] Journal of Medicinal Chemistry, 1999, vol. 42, # 14, p. 2706 - 2715
[3] Journal of Medicinal Chemistry, 1999, vol. 42, # 24, p. 4981 - 5001
[4] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 24, p. 5345 - 5352
[5] Patent: WO2007/46550, 2007, A1. Location in patent: Page/Page column 117
1-BENZYL-4-(N-BOC-AMINO) PIPERIDINE 98Supplier
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