Hydrochloric Acid → N-((3R,5S)-5-Hydroxymethyl-pyrrolidin-3-yl)-acetamide hydrochloride

HRID 1012018Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1012018
[H-].[Al+3].[Li+].[H-].[H-].[H-].CO[C:9]([C@@H:11]1[CH2:15][C@@H:14]([N:16]=[N+]=[N-])[CH2:13][N:12]1C(OC(C)(C)C)=O)=[O:10].C(=O)([O-])[O-].[Na+].[Na+].[C:32](OC(=O)C)(=[O:34])[CH3:33].[ClH:39]>C1COCC1.O1CCOCC1.O>[ClH:39].[OH:10][CH2:9][C@H:11]1[NH:12][CH2:13][C@H:14]([NH:16][C:32](=[O:34])[CH3:33])[CH2:15]1

Komponenten

9

Versuchsvorschrift

To an ice-cold suspension of lithium aluminium hydride (0.6 g, 15 mmol) in THF (10 ml) was added a solution of (2S,4R)-4-azido-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (1.0 g, 4 mmol) in THF (5 mL) and the mixture stirred for 1 h. Water was then cautiously added to the reaction and the mixture filtered and concentrated. The residue was then taken up in CH2Cl2 (10 ml) and saturated sodium carbonate (10 ml) and acetic anhydride (0.3 ml, 3 mmol) added. The mixture was stirred for 2 h after which time the organic was collected, dried (Na2SO4) and concentrated. The residue (0.6 g, 2 mmol) was then treated with 4 M hydrochloric acid in dioxane (5 ml) for 1 h, evaporation of the solvent afforded the title compound (0.5 g, 80%) as a yellow solid. MS: 159.1 (MH+).

Aufarbeitung

  1. filtrationthe mixture filtered
  2. concentrationconcentrated
  3. stirringThe mixture was stirred for 2 h after which time the
  4. customorganic was collected
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated
  7. customevaporation of the solvent

Quellen und Nachweise

ORD-Eintrag
ord-ebf22027614840a7862850e9751d0736
Quelldatensatz
uspto-grants-2011_07
Patentnummer
US07977358B2

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