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L-Serine → N-[(1,1-Dimethylethoxy)carbonyl]-L-phenylalanyl-L-serine

HRID 2269624
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2269624
CN(C=O)C.[NH:6]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[C@H:7]([C:15]([O:17]N1C(=O)CCC1=O)=O)[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[NH2:32][C@H:33]([C:36]([OH:38])=[O:37])[CH2:34][OH:35].CCN(CC)CC>>[NH:6]([C:25]([O:27][C:28]([CH3:29])([CH3:30])[CH3:31])=[O:26])[C@H:7]([C:15]([NH:32][C@H:33]([C:36]([OH:38])=[O:37])[CH2:34][OH:35])=[O:17])[CH2:8][C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 5951L-Serine2×HCID 6228DimethylformamideHCID 8471Triethylamine2×HCID 107447tert-butyl (S)-(1-benzyl-2-((2,5-dioxo-1-pyrrolidinyl)oxy)-2-oxoethyl)carbamate

Produkt 1

HCID 13892838N-[(1,1-Dimethylethoxy)carbonyl]-L-phenylalanyl-L-serineAusbeute 31 %

Versuchsvorschrift

In a 10 ml solution of DMF containing 500 mg (1.38 mmol) of Boc-Phe-OSu was added 5 ml of an aqueous solution of H-Ser-OH.Et3N [preparation from 290 mg (2.76 mmol) of H-Ser-OH and 384 μl (2.76 mmol) of Et3N] and the mixture was stirred for 14 hr. The reaction mixture was evaporated and the residue was dissolved in ethyl acetate and washed with 1N-HCl and saturated sodium chloride aqueous solution, successively, together with salting out. The resultant solution was dried over anhydrous sodium sulfate, evaporated under reduced pressure, and the resulting residue was purified with a silica gel column chromatography (CHCl3:MeOH). The eluate was mixed with ether and n-hexane to give crystals of 150 mg of the title compound with yield of 31%.

Aufarbeitung

  1. customThe reaction mixture was evaporated
  2. dissolutionthe residue was dissolved in ethyl acetate
  3. washwashed with 1N-HCl and saturated sodium chloride aqueous solution
  4. dry with materialThe resultant solution was dried over anhydrous sodium sulfate
  5. customevaporated under reduced pressure
  6. customthe resulting residue was purified with a silica gel column chromatography (CHCl3:MeOH)
  7. additionThe eluate was mixed with ether and n-hexane

Quellen und Nachweise

ORD-Eintrag
ord-c7e4c3b746fd44b88d4bdf79eaf48e97
Quelldatensatz
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06329502B1

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