Potassium sodium tartarate → (2S,4R)-[4-tert-butoxy-1-(naphthalene-2-sulfonyl)-pyrrolidin-2-yl]-methanol

HRID 1006836Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1006836
[H-].[H-].[H-].[H-].[Li+].[Al+3].C([O:14][C:15]([C@@H:17]1[CH2:21][C@@H:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])[CH2:19][N:18]1[S:27]([C:30]1[CH:39]=[CH:38][C:37]2[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=2)[CH:31]=1)(=[O:29])=[O:28])=O)C1C=CC=CC=1.C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>CCOCC>[C:23]([O:22][C@H:20]1[CH2:19][N:18]([S:27]([C:30]2[CH:39]=[CH:38][C:37]3[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=3)[CH:31]=2)(=[O:29])=[O:28])[C@H:17]([CH2:15][OH:14])[CH2:21]1)([CH3:26])([CH3:25])[CH3:24]

Komponenten

5

Versuchsvorschrift

LAH reduction: To a slurry of lithium aluminium hydride (0.72 g) in Et2O (120 ml) was added a solution of (2S,4R)-4-tert-butoxy-1-(naphthalene-2-sulfonyl)-pyrrolidine-2-carboxylic acid benzyl ester (9.0 g) in Et2O (80 ml) dropwise at −15° C. within 0.5 h. The suspension was stirred for 2 h at the same temperature, then a saturated solution of potassium-sodium tartrate (10 ml) was added dropwise. The slurry was filtered through a pad of filter aid and was washed with Et2O. The combined filtrates were washed with brine, dried over magnesium sulphate and concentrated. The residue was crystallized from acetone/Et2O/hexane to obtain (2S,4R)-[4-tert-butoxy-1-(naphthalene-2-sulfonyl)-pyrrolidin-2-yl]-methanol (6.1 g) as a colorless solid, mp 124-125° C.; MS 363 (M).

Aufarbeitung

  1. filtrationThe slurry was filtered through a pad of filter aid
  2. washwas washed with Et2O
  3. washThe combined filtrates were washed with brine
  4. dry with materialdried over magnesium sulphate
  5. concentrationconcentrated
  6. customThe residue was crystallized from acetone/Et2O/hexane

Quellen und Nachweise

ORD-Eintrag
ord-bbc519ad5aa94695a777f7d30aa803a9
Quelldatensatz
uspto-grants-2004_09
Patentnummer
US06790860B2

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