Benzyl Bromide → Boc-DTrp-OBzl

HRID 2082210

Reaktionsgleichung

Reaktionsgleichung von HRID 2082210
[NH:1]([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[C@@H:2]([C:13]([OH:15])=[O:14])[CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[NH:6][CH:5]=1.[CH2:23](Br)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.C(N(C(C)C)CC)(C)C>CN(C=O)C>[NH:1]([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[C@@H:2]([C:13]([O:15][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:14])[CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[NH:6][CH:5]=1

Komponenten

5

Edukt 3

HCID 7498Benzyl BromideHCID 81531DiisopropylethylamineHCID 111050N-((tert-Butoxy)carbonyl)-D-tryptophan

Produkt 1

HCID 10739405Boc-DTrp-OBzlAusbeute 95 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To an ice-cooled solution of Boc-D-Trp-OH (8.61 g) in DMF (100 ml) were added benzyl bromide (7.19 g) and diisopropylethylamine (4.02 g). The solution was stirred for two hours at the same temperature and overnight at room temperature. After evaporation, the residue was extracted with ethyl acetate. The organic layer was washed successively with water, sodium hydrogencarbonate solution, 0.5 hydrochlolic acid, and sodium chloride solution, and dried over magnesium sulfate. Evaporation gave Boc-D-Trp-OBzl (10.6 g) as a crystalline mass.

Aufarbeitung

  1. customAfter evaporation
  2. extractionthe residue was extracted with ethyl acetate
  3. washThe organic layer was washed successively with water, sodium hydrogencarbonate solution, 0.5 hydrochlolic acid, and sodium chloride solution
  4. dry with materialdried over magnesium sulfate
  5. customEvaporation

Quellen und Nachweise

ORD-Eintrag
ord-b08df90ed268472484e2250dbf5f4ea9
Quelldatensatz
uspto-grants-1993_02
Patentnummer
US05187156

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