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Tetrabutylammonium Fluoride → HCID 59063640, Verbindung

HRID 49404
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 49404
C([Si](C)(C)[O:6][C@H:7]([C:25]1[CH:26]=[CH:27][C:28]([NH:31][C:32](=[O:34])[CH3:33])=[N:29][CH:30]=1)[CH2:8][NH:9][CH2:10][CH2:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([C:19]2[N:20]=[C:21]([CH3:24])[S:22][CH:23]=2)=[CH:15][CH:14]=1)(C)(C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[OH:6][C@H:7]([C:25]1[CH:26]=[CH:27][C:28]([NH:31][C:32](=[O:34])[CH3:33])=[N:29][CH:30]=1)[CH2:8][NH:9][CH2:10][CH2:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([C:19]2[N:20]=[C:21]([CH3:24])[S:22][CH:23]=2)=[CH:17][CH:18]=1
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Komponenten

4

Edukt 2

HCID 2724141Tetrabutylammonium FluorideHCID 69743740(R)-N-[5-(1-(tert-Butyl-dimethyl-silanyloxy)-2-{2-[4-(2-methyl-thiazol-4-yl)-phenoxy]-ethylamino}-ethyl)-pyridin-2-yl]-acetamide

Produkt 1

HCID 59063640HCID 59063640, VerbindungAusbeute 83,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of (R)-N-[5-(1-(tert-butyl-dimethyl-silanyloxy)-2-{2-[4-(2-methyl-thiazol-4-yl)-phenoxy]-ethylamino}-ethyl)-pyridin-2-yl]-acetamide (115 mg, 0.218 mmol) in tetrahydrofuran (1.5 mL) was added tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 0.65 mL, 0.65 mmol) at room temperature. The resulting solution was allowed to stir for about two and one-half hours, and the reaction mixture was then partitioned between ethyl acetate and water. The pH of the mixture was adjusted to about 10-11, and the aqueous phase was then extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting crude material was purified by column chromatography (methylene chloride to 20% methanol/methylene chloride) to afford 75 mg (83%) of the desired product. LRMS ([M+1]+): 413.2.

Aufarbeitung

  1. customthe reaction mixture was then partitioned between ethyl acetate and water
  2. extractionthe aqueous phase was then extracted with ethyl acetate
  3. washThe combined organic extracts were washed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe resulting crude material was purified by column chromatography (methylene chloride to 20% methanol/methylene chloride)

Quellen und Nachweise

ORD-Eintrag
ord-c23a80a61b884a94a1b5a7f2d30b582e
Quelldatensatz
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06706743B2

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