Pyridine → (2S)-2-(((tert-butoxy)carbonyl)amino)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanoic acid

HRID 393049

Reaktionsgleichung

Reaktionsgleichung von HRID 393049
FC(F)(F)C(OC1C(OC(=O)C(F)(F)F)=C(I)C=CC=1)=O.[CH3:22][C:23]([CH3:37])([O:25][C:26]([NH:28][C@H:29]([C:34]([OH:36])=[O:35])[CH2:30]C(=O)N)=[O:27])[CH3:24].[N:38]1C=CC=CC=1.C(=O)([O-])O.[Na+].[CH:49]1[C:61]2[CH:60]([CH2:62][O:63][C:64](ON3C(=O)CCC3=O)=[O:65])[C:59]3[C:54](=[CH:55][CH:56]=[CH:57][CH:58]=3)[C:53]=2[CH:52]=[CH:51][CH:50]=1>CN(C)C=O.O>[CH3:37][C:23]([CH3:22])([O:25][C:26]([NH:28][C@H:29]([C:34]([OH:36])=[O:35])[CH2:30][NH:38][C:64]([O:63][CH2:62][CH:60]1[C:61]2[CH:49]=[CH:50][CH:51]=[CH:52][C:53]=2[C:54]2[C:59]1=[CH:58][CH:57]=[CH:56][CH:55]=2)=[O:65])=[O:27])[CH3:24]

Komponenten

7

Edukt 5

HCID 1049PyridineHCID 82035N2-((tert-Butoxy)carbonyl)-L-asparagineHCID 134122N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 516892Sodium BicarbonateHCID 12041285Bistrifluoroacetoxyiodobenzene

Produkt 1

HCID 7019527(2S)-2-(((tert-butoxy)carbonyl)amino)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanoic acidAusbeute 88 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 21962138N,N-Dimethylformamide--water (1/1)Lösungsmittel

Versuchsvorschrift

Bis(trifluoroacetoxy)iodobenzene (44.4 g, 103.2 mmol) was added to a solution of N-[(1,1-dimethylethoxy)carbonyl]-L-asparagine (Boc-Asn; 20.00 g, 86.1 mmol) in N,N-dimethylformamide/water (2:1; 300 mL). The solution was stirred at room temperature for 30 min and then pyridine (10 mL, 123.6 mmol) was added. The solution was stirred at room temperature for 4.5 h and then the solvent was evaporated (45° C., ˜0.5 mm Hg). The residue was dissolved in acetone/water (1:1; 400 mL) and sodium hydrogen carbonate (31.8 g, 378.5 mmol) and 1-[[(9H-fluoren-9-ylmethoxy)carbonyl]oxy]-2,5-pyrrolidinedione (Fmoc-OSu; 34.74 g, 103.0 mmol) were added. The mixture was stirred at room temperature overnight, then the acetone was evaporated and the mixture was acidified to pH 1 with 1 M HCl and extracted with ethyl acetate (200 mL, then 100 mL). The combined organic layers were washed with brine (3×50 mL), dried (Na2SO4), filtered, evaporated (45° C., ˜0.5 mm Hg), and chromatographed (50-60% ethyl acetate/hexanes) to give N-[(1,1-dimethylethoxy)carbonyl]-3-[(9H-fluoren-9-ylmethoxy)carbonyl]amino-L-alanine (32.33 g, 88%) as a white solid.

Aufarbeitung

  1. stirringThe solution was stirred at room temperature for 4.5 h
  2. customthe solvent was evaporated (45° C., ˜0.5 mm Hg)
  3. dissolutionThe residue was dissolved in acetone/water (1:1; 400 mL)
  4. stirringThe mixture was stirred at room temperature overnight
  5. customthe acetone was evaporated
  6. extractionextracted with ethyl acetate (200 mL
  7. washThe combined organic layers were washed with brine (3×50 mL)
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. customevaporated (45° C., ˜0.5 mm Hg)
  11. customchromatographed (50-60% ethyl acetate/hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-3edf7753dd6b4f4ca872c1e385d812b5
Quelldatensatz
uspto-grants-2004_10
Patentnummer
US06803384B2

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