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Tetrabutylammonium Fluoride → HCID 57504671, Verbindung

HRID 1098198
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1098198
[F-].C([N+](CCCC)(CCCC)CCCC)CCC.[Si]([O:26][C@@H:27]([CH2:39][O:40][CH:41]([CH3:43])[CH3:42])[C:28]([NH:30][C:31]1[CH:36]=[CH:35][C:34]([S:37][CH3:38])=[CH:33][N:32]=1)=[O:29])(C(C)(C)C)(C)C>O1CCCC1>[OH:26][C@@H:27]([CH2:39][O:40][CH:41]([CH3:43])[CH3:42])[C:28]([NH:30][C:31]1[CH:36]=[CH:35][C:34]([S:37][CH3:38])=[CH:33][N:32]=1)=[O:29]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 2724141Tetrabutylammonium FluorideHCID 57504670(S)-2-(tert-butyldimethylsilyloxy)-3-isopropoxy-N-(5-(methylthio)pyridin-2-yl)propanamide

Produkt 1

HCID 57504671HCID 57504671, VerbindungAusbeute 88 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of tetrabutylammonium fluoride (1M in THF) (10.04 mL, 10.04 mmol) was added in one portion to a stirred solution of (S)-2-(tert-butyldimethylsilyloxy)-3-isopropoxy-N-(5-(methylthio)pyridin-2-yl)propanamide (Intermediate AI1) in tetrahydrofuran (50 mL). The resulting solution was stirred at ambient temperature for 30 minutes. The majority of the THF was evaporated in vacuo. The residue was diluted with EtOAc (100 mL), washed sequentially with water (25 mL) and saturated brine (25 mL). The organic layer was dried (MgSO4), filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 30 to 50% EtOAc in isohexane to afford the product (2.38 g, 88%). 1H NMR (400 MHz, DMSO) δ 1.03-1.07 (6H, m), 3.28 (3H, s), 3.53-3.64 (3H, m), 4.19-4.22 (1H, m), 5.95 (1H, d), 7.77-7.80 (1H, d), 8.04-8.06 (1H, d), 8.24-8.25 (1H, s), 9.60 (1H, s); m/z (ES+) (M+H)+=271; HPLC tR=1.74 min.

Aufarbeitung

  1. customThe majority of the THF was evaporated in vacuo
  2. additionThe residue was diluted with EtOAc (100 mL)
  3. washwashed sequentially with water (25 mL) and saturated brine (25 mL)
  4. dry with materialThe organic layer was dried (MgSO4)
  5. filtrationfiltered
  6. customevaporated
  7. customto afford crude product
  8. customThe crude product was purified by flash silica chromatography, elution gradient 30 to 50% EtOAc in isohexane

Quellen und Nachweise

ORD-Eintrag
ord-081a456007e144a6945f979ce1199f30
Quelldatensatz
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08143263B2

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