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224824-22-0

224824-22-0 Structure

224824-22-0 Structure
IdentificationBack Directory
[Name]

(S)-(4-(2-((tert-Butoxycarbonyl)aMino)-3-Methoxy-3-oxopropyl)phenyl)boronic acid
[CAS]

224824-22-0
[Synonyms]

Boc-4-borono-L-phenylalanine methyl ester
(S)-4-[2-(Boc-amino)-3-methoxy-3-oxopropyl]phenylboronic Acid
(S)-4-(2-(tert-butoxycarbonylamino)-3-methoxy-3-oxopropyl)ph...
4-Borono-N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanine methyl ester
N-(tert-Butoxycarbonyl)-4-(dihydroxyboryl)-L-phenylalanine methyl ester
L-Phenylalanine, 4-borono-N-[(1,1-dimethylethoxy)carbonyl]-, 1-methyl ester
(S)-(4-(2-((tert-Butoxycarbonyl)amno)-3-methoxy-3-oxopropyl)phenyl)boronic acid
(S)-(4-(2-((tert-Butoxycarbonyl)aMino)-3-Methoxy-3-oxopropyl)phenyl)boronic acid
[4-[(2S)-3-methoxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-oxopropyl]phenyl]boronic acid
[Molecular Formula]

C15H22BNO6
[MDL Number]

MFCD10698492
[MOL File]

224824-22-0.mol
[Molecular Weight]

323.15
Chemical PropertiesBack Directory
[density ]

1.20±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

8.56±0.16(Predicted)
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-(4-(2-((tert-Butoxycarbonyl)aMino)-3-Methoxy-3-oxopropyl)phenyl)boronic acid(224824-22-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

(S)-methyl 2-(tert-butoxycarbonylamino)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate

220587-29-1

(S)-(4-(2-((tert-Butoxycarbonyl)aMino)-3-Methoxy-3-oxopropyl)phenyl)boronic acid

224824-22-0

Methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propionate (67.0 g, 165 mmol) was used as a raw material and dissolved in acetone (700 mL). To this solution, sodium periodate (71.0 g, 330 mmol), ammonium acetate (25.0 g, 330 mmol) and water (300 mL) were added sequentially and the reaction was stirred for 55 hours at room temperature. After completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure and extracted by adding ethyl acetate. The organic phase was washed sequentially with water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the resulting solid was washed with a mixed solvent of petroleum ether/ethyl acetate (1:10, v/v) and dried to afford the target product (S)-(4-(2-((tert-butoxycarbonyl)amino)-3-methoxy-3-oxopropyl)phenylboronic acid (29 g, 55% yield).1H NMR (CDCl3, 400 MHz) δ: 7.71-7.56 (m 2H), 7.25-7.16 (m, 2H), 4.39-4.37 (m, 1H), 3.71 (s, 3H), 3.14-3.10 (m, 1H), 2.96-2.90 (m, 1H), 1.40 (s, 9H). MS (ESI) m/z 224 (M + H - Boc)+.

[References]

[1] Angewandte Chemie - International Edition, 2014, vol. 53, # 6, p. 1669 - 1673
[2] Angew. Chem., 2014, vol. 126, # 6, p. 1695 - 1699,5
[3] Patent: US2015/51395, 2015, A1. Location in patent: Paragraph 0134-0135
[4] Patent: US2016/244451, 2016, A1. Location in patent: Paragraph 0144; 0145; 0146
[5] Patent: JP2016/37467, 2016, A. Location in patent: Paragraph 0060
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