BOC-D-4,4'-BIPHENYLALANINE
BOC-D-4,4'-BIPHENYLALANINE Basic information
- Product Name:
- BOC-D-4,4'-BIPHENYLALANINE
- Synonyms:
-
- BOC-D-PHE(4-PHENYL)-OH
- BOC-D-BPH-OH
- BOC-D-BIP(4,4')-OH
- BOC-D-BIP-OH
- BOC-D-ALA(4,4'-BIPHENYL)-OH
- BOC-3-(4-BIPHENYLYL)-D-ALANINE
- BOC-4-PHENYL-D-PHENYLALANINE
- BOC-4-PHENYL-D-PHE-OH
- CAS:
- 128779-47-5
- MF:
- C20H23NO4
- MW:
- 341.4
- Product Categories:
-
- Phenylalanine analogs and other aromatic alpha amino acids
- Amino Acids
- a-amino
- Biphenyl & Diphenyl ether
- Amino Acid Derivatives
- Mol File:
- 128779-47-5.mol
BOC-D-4,4'-BIPHENYLALANINE Chemical Properties
- Boiling point:
- 528.2±50.0 °C(Predicted)
- Density
- 1.161±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Store in freezer, under -20°C
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 3.88±0.10(Predicted)
- Appearance
- White to off-white Solid
- CAS DataBase Reference
- 128779-47-5(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- HS Code
- 2922498590
BOC-D-4,4'-BIPHENYLALANINE Usage And Synthesis
Uses
Boc-D-4,4'-biphenylalanine is used as a reagent in the synthesis of pyrrolopyrimidine inhibitors of Akt as antitumor agents. Boc-D-4,4'-biphenylalanine is also used in the preparation of (-)-Bestatin-based inhibitors.
Synthesis
24424-99-5
155760-02-4
119273-61-9
To a mixed solution of tetrahydrofuran (THF) (80 mL) and water (80 mL) of (S)-3-([1,1'-biphenyl]-4-yl)-2-aminopropanoic acid (25) (5 g, 20.72 mmol) was added di-tert-butyl dicarbonate (BOC2O) (5.77 mL, 24.87 mmol) and sodium hydroxide (NaOH) (1.077 g. 26.9 mmol). The reaction mixture was stirred at room temperature for 6 hours before being cooled to 0 °C and the pH was adjusted to about 6-7 by slowly adding 1.5 N aqueous hydrochloric acid (HCl) to quench the reaction. Subsequently, the reaction mixture was extracted with ethyl acetate (EtOAc) (3 x 50 mL). The combined organic layers were washed sequentially with brine (50 mL) and water (50 mL), dried over anhydrous sodium sulfate and concentrated to give the crude product as a colloidal off-white solid. The crude product was purified by washing with petroleum ether (PE) with 10% ethyl acetate (4 x 20 mL). The resulting white solid was filtered and dried under vacuum to afford (S)-3-([1,1'-biphenyl]-4-yl)-2-((tert-butoxycarbonyl)amino)propionic acid (26) (6.5 g, 19.04 mmol, 92% yield). The product was analyzed by 1H NMR (400 MHz, DMSO-d6) and mass spectrometry (ESI) to confirm the structure.1H NMR data: δ 7.67-7.62 (m, 2H), 7.58 (d, J=8.5 Hz, 2H), 7.50-7.43 (m, 2H), 7.39-7.31 (m, 3H), 7.10 (d, J=8.0 Hz. 1H), 4.17-4.07 (m, 1H), 3.07 (dd, J=13.6,4.5Hz, 1H), 2.88 (dd, J=13.6,10.0Hz, 1H), 1.37-1.23 (m, 9H). Mass spectral data: 340.2 ([M-1]-).
References
[1] Tetrahedron Letters, 2018, p. 4267 - 4271
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