Water → 6-(bis((1-methyl-1H-imidazol-2-yl)methyl)amino)hexanoic acid

HRID 1043372Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1043372
N(C(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O)[C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][CH2:5][CH2:6][NH2:7].Cl.[CH3:29][N:30]1[CH:34]=[CH:33][N:32]=[C:31]1[CH:35]=O.[BH-](O[C:47]([CH3:49])=O)(OC(C)=O)OC(C)=O.[Na+].O>ClCCCl>[CH3:29][N:30]1[CH:34]=[CH:33][N:32]=[C:31]1[CH2:35][N:7]([CH2:35][C:31]1[N:30]([CH3:29])[CH:47]=[CH:49][N:32]=1)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:8]([OH:10])=[O:9]

Komponenten

6

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of Fmoc-Lys-OH.HCl (1.822 g, 4.5 mmol) and 1-methyl-1H-imidazole-2-carbaldehyde (1.10 g, 10 mmol) in DCE (50 mL) was stirred at 75° C. for 30 min under nitrogen. The reaction mixture was cooled to 0° C., and treated with NaBH(OAc)3 (3.165 g, 15 mmol). The reaction mixture was stirred at room temperature for overnight and decomposed with water. The reaction mixture was extracted with DCM, the organic layer dried and concentrated under reduced pressure. The residue was purified by flash chromatography over silica gel to afford (S)-2-4(9H-fluoren-9-yl)methoxy)carbonylamino)-6-(bis((1-methyl-1H-imidazol-2-yl)methyl)amino)hexanoic acid (2.30 g, 92%). MS (ESI), 557 (M+H)+.

Aufarbeitung

  1. extractionThe reaction mixture was extracted with DCM
  2. customthe organic layer dried
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was purified by flash chromatography over silica gel

Quellen und Nachweise

ORD-Eintrag
ord-822e752198f54147a815e25fff1d54e9
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08562945B2

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