Hydrochloric Acid → (R)-N-hydroxy-2-methyl-2-(methylsulfonyl)-4-(2-oxo-4-(phenylethynyl) pyridin-1(2H)-yl)butanamide

HRID 84312Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 84312
Cl.[CH3:2][C@@:3]([S:31]([CH3:34])(=[O:33])=[O:32])([CH2:14][CH2:15][N:16]1[CH:21]=[CH:20][C:19]([C:22]#[C:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)=[CH:18][C:17]1=[O:30])[C:4]([NH:6][O:7]C1CCCCO1)=[O:5]>O1CCOCC1>[OH:7][NH:6][C:4](=[O:5])[C@:3]([CH3:2])([S:31]([CH3:34])(=[O:33])=[O:32])[CH2:14][CH2:15][N:16]1[CH:21]=[CH:20][C:19]([C:22]#[C:23][C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=2)=[CH:18][C:17]1=[O:30]

Komponenten

4

Versuchsvorschrift

A solution of 1.0 M aqueous HCl (10 ml) was added slowly to a solution of (2R)-2-methyl-2-(methylsulfonyl)-4-(2-oxo-4-(phenylethynyl)pyridin-1(2H)-yl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide (107 mg, 0.226 mmol) in 1,4-dioxane (20 mL) at room temperature. The reaction mixture was allowed to stir at room temperature overnight. After 18 hours the reaction was concentrated to low volume then redissolved in methanol (20 ml) and concentrated in vacuo to afford a light-yellow solid. Yield 71 mg, 81%. MS (APCI) m/z 389.4 (M+H), 1H NMR (400 MHz, DMSO-d6) δ ppm 1.46 (none, 3 H) 1.53 (s, 3 H) 2.03-2.17 (m, 1 H) 2.33-2.45 (m, 1 H) 3.07 (s, 3 H) 3.71 (td, J=11.90, 4.88 Hz, 1 H) 3.96-4.14 (m, 1 H) 6.35 (dd, J=6.93, 1.85 Hz, 1 H) 6.56 (d, J=1.76 Hz, 1 H) 7.36-7.48 (m, 3 H) 7.51-7.61 (m, 2 H) 7.69 (d, J=7.02 Hz, 1 H) 11.05 (br. s., 1 H)

Aufarbeitung

  1. concentrationAfter 18 hours the reaction was concentrated to low volume
  2. dissolutionthen redissolved in methanol (20 ml)
  3. concentrationconcentrated in vacuo
  4. customto afford a light-yellow solid

Quellen und Nachweise

ORD-Eintrag
ord-abbcad299d694b31aa5a776431a97874
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08846933B2

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