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Dimethylformamide → (S)-2-(benzoyloxy)-4-(benzyloxycarbonylamino)butanoic acid

HRID 1949613
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1949613
[C:1]([O:11]C1C=CC=CC=1[N+]([O-])=O)([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=O.C1CN([P+](ON2N=N[C:40]3[CH:41]=[CH:42][CH:43]=[CH:44][C:39]2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.C(OC(N1[CH2:64][C:63]([OH:68])([C:65]([OH:67])=[O:66])C1)=O)(C)(C)C.CC[N:71]([CH:75](C)C)C(C)C.CN([CH:81]=[O:82])C>>[C:81]([O:68][C@@H:63]([CH2:64][CH2:75][NH:71][C:1]([O:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:11])[C:65]([OH:67])=[O:66])(=[O:82])[C:39]1[CH:40]=[CH:41][CH:42]=[CH:43][CH:44]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 6228DimethylformamideHCID 81531DiisopropylethylamineHCID 2724699PyBOPHCID 54130325Nitrophenyl benzyl carbonateHCID 598596891-[(Tert-butoxy)carbonyl]-3-hydroxyazetidine-3-carboxylic acid

Produkt 1

HCID 58503128
(S)-2-(benzoyloxy)-4-(benzyloxycarbonylamino)butanoic acid

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a cold solution of 200 mg of 3′,4′,3′″,4′″-tetra-dehydro-3,2′,6′,2′″,6′″-Cbz-Neomycin (1 (3 from Example 4), 0.16 mmol) in 4.0 mL DMF was added 103 mg PyBOP (0.1972 mmol) and 1-(tert-butoxycarbonyl)-3-hydroxyazetidine-3-carboxylic acid (0.1972 mmol). The flask was then cooled to 0° C. and 47.8 μl DIPEA (0.2793 mmol) was added. The reaction was allowed to stir at room temperature overnight then LCMS was used to confirm product formation and the absence of starting material. The reaction was then quenched with 10-20 mL 1 M citric acid and desired product was extracted into 10 mL ethyl acetate. The organic layers were washed with a second 10 mL 1 M citric acid, brine and dried while stirring with MgSO4. Concentration under vacuum provided crude intermediate (2) that was used in the next reaction without further purification. MS: m/z (M+Na) calc: 1438.57, obs: 1438.4.

Aufarbeitung

  1. customThe reaction was then quenched with 10-20 mL 1 M citric acid and desired product
  2. extractionwas extracted into 10 mL ethyl acetate
  3. washThe organic layers were washed with a second 10 mL 1 M citric acid, brine
  4. customdried
  5. stirringwhile stirring with MgSO4
  6. concentrationConcentration under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-39e9858fd169485aba4062a3610e9624
Quelldatensatz
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08399419B2

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