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Sodium Bicarbonate → 1-[6-(5-{2-cyclopentyl-1-[5-(methylsulfanyl)pyridin-2-yl]ethyl}-1H-pyrrol-2-yl)pyridin-3-yl]ethane-1,2-diol

HRID 1882098
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1882098
[Si]([O:8][CH:9]([C:19]1[CH:20]=[CH:21][C:22]([C:25](=O)[CH2:26][CH2:27][C:28](=O)[CH:29]([C:36]2[CH:41]=[CH:40][C:39]([S:42][CH3:43])=[CH:38][N:37]=2)[CH2:30][CH:31]2[CH2:35][CH2:34][CH2:33][CH2:32]2)=[N:23][CH:24]=1)[CH2:10][O:11][Si](C(C)(C)C)(C)C)(C(C)(C)C)(C)C.C([O-])(=O)C.[NH4+:50].C(=O)([O-])O.[Na+]>C(O)(=O)C.C(OCC)(=O)C>[CH:31]1([CH2:30][CH:29]([C:28]2[NH:50][C:25]([C:22]3[N:23]=[CH:24][C:19]([CH:9]([OH:8])[CH2:10][OH:11])=[CH:20][CH:21]=3)=[CH:26][CH:27]=2)[C:36]2[CH:41]=[CH:40][C:39]([S:42][CH3:43])=[CH:38][N:37]=2)[CH2:35][CH2:34][CH2:33][CH2:32]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 516892Sodium BicarbonateHCID 517165Ammonium AcetateHCID 593314141-[5-(1,2-Bis{[tert-butyl(dimethyl)silyl]oxy}ethyl)pyridin-2-yl]-6-cyclopentyl-5-[5-(methylsulfanyl)pyridin-2-yl]hexane-1,4-dione

Produkt 1

HCID 593313131-[6-(5-{2-cyclopentyl-1-[5-(methylsulfanyl)pyridin-2-yl]ethyl}-1H-pyrrol-2-yl)pyridin-3-yl]ethane-1,2-diolAusbeute 53,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 176Acetic AcidLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

To a solution of 1-[5-(1,2-bis{[tert-butyl(dimethyl)silyl]oxy}ethyl)pyridin-2-yl]-6-cyclopentyl-5-[5-(methylsulfanyl)pyridin-2-yl]hexane-1,4-dione (682 mg) in acetic acid (7 mL) was added ammonium acetate (1.26 g), and the mixture was stirred at 110° C. for 45 min. After cooling to room temperature, the mixture was neutralized with saturated aqueous sodium hydrogen carbonate solution. The reaction mixture was diluted with ethyl acetate and washed with water. The ethyl acetate layer was dried (MgSO4) and concentrated. To a solution of the obtained residue in tetrahydrofuran (4 mL) was added tetrabutylammonium fluoride (1M tetrahydrofuran solution, 8.16 mL), and the mixture was stirred at room temperature for 1.5 hr. The reaction mixture was diluted with ethyl acetate, and washed with saturated brine. The ethyl acetate layer was dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and the title compound (230 mg, yield 53%) was obtained as a colorless amorphous solid from a fraction eluted with ethyl acetate-hexane (99:1, volume ratio). MS: 424 (MH+).

Aufarbeitung

  1. temperatureAfter cooling to room temperature
  2. washwashed with water
  3. dry with materialThe ethyl acetate layer was dried (MgSO4)
  4. concentrationconcentrated
  5. additionTo a solution of the obtained residue in tetrahydrofuran (4 mL) was added tetrabutylammonium fluoride (1M tetrahydrofuran solution, 8.16 mL)
  6. stirringthe mixture was stirred at room temperature for 1.5 hr
  7. additionThe reaction mixture was diluted with ethyl acetate
  8. washwashed with saturated brine
  9. dry with materialThe ethyl acetate layer was dried (MgSO4)
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-4208bd663fe6469b99fb15f014ba2e89
Quelldatensatz
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08318746B2

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