Triacetoxyperiodinane → 4-Benzyloxy-2-formyl-2,3-dihydro-benzofuran-6-carboxylic acid (1-methyl-1H-pyrazol-3-yl)-amide

HRID 1643701Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1643701
[CH3:1][N:2]1[CH:6]=[CH:5][C:4]([NH:7][C:8]([C:10]2[CH:20]=[C:19]([O:21][CH2:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:13]3[CH2:14][CH:15]([CH2:17][OH:18])[O:16][C:12]=3[CH:11]=2)=[O:9])=[N:3]1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>C(Cl)Cl>[CH3:1][N:2]1[CH:6]=[CH:5][C:4]([NH:7][C:8]([C:10]2[CH:20]=[C:19]([O:21][CH2:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:13]3[CH2:14][CH:15]([CH:17]=[O:18])[O:16][C:12]=3[CH:11]=2)=[O:9])=[N:3]1

Komponenten

4

Versuchsvorschrift

To a suspension of 4-benzyloxy-2-hydroxymethyl-2,3-dihydro-benzofuran-6-carboxylic acid (1-methyl-1H-pyrazol-3-yl)-amide (222a) (1.05 g, 2.77 mmol) in CH2Cl2 (25 mL) was added Dess-Martin periodinane (1.41 g, 3.32 mmol) at 0° C. The mixture was stirred at room temperature for 2 h. The reaction was quenched with saturated aqueous NaHCO3, extracted with 3×EtOAc, dried over Na2SO4, concentrated, and purified by flash column chromatography eluting with 55-100% EtOAc in hexanes to give a yellow foam (850 mg).

Aufarbeitung

  1. customThe reaction was quenched with saturated aqueous NaHCO3
  2. extractionextracted with 3×EtOAc
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated
  5. custompurified by flash column chromatography
  6. washeluting with 55-100% EtOAc in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-124565d496e741eabd8d9f2a1cfe3a61
Quelldatensatz
uspto-grants-2012_02
Patentnummer
US08119624B2

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