Reaktion #1869179

ord-d47409756b99485191fa800c4bb3463b

Reaktionsgleichung

Cl
hydrochloric acid
CCCCN1C(=O)NC(=O)C12CCNCC2
compound
CCCCN1C(=O)NC(=O)C12CCNCC2
1-butyl-1,3,8-triazaspiro[4.5]decane-2,4-dione
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)(C)OC(=O)OC(=O)[O-]
t-butyl dicarbonate
CCCCN1C(=O)NC(=O)C12CCN(C(=O)OC(C)(C)C)CC2
title compound
Ausbeute 89.0%
CCCCN1C(=O)NC(=O)C12CCN(C(=O)OC(C)(C)C)CC2
1-butyl-8-(t-butoxycarbonyl)-1,3,8-triazaspiro-[4.5]decane-2,4-dione
Ausbeute 89.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe aqueous layer was extracted three times with ethyl acetate
  2. 2
    WaschenThe combined organic layer was washed with a saturated aqueous solution of sodium chloride
  3. 3
    Trocknendried over an anhydrous magnesium sulfate
  4. 4
    Einengenconcentrated
  5. 5
    SonstigeThe residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1→1:2)

Vorschrift

To a solution of the compound prepared in Example 5 (326 mg) in water (3 mL) were added potassium carbonate and t-butyl dicarbonate (348 mg) subsequently, and the mixture was stirred for 1 hour at room temperature. The reaction mixture was neutralized with 1N hydrochloric acid. The aqueous layer was extracted three times with ethyl acetate. The combined organic layer was washed with a saturated aqueous solution of sodium chloride, dried over an anhydrous magnesium sulfate and then concentrated. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1→1:2) to give the title compound (419 mg) having the following physical data.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07498323B2uspto-grants-2009_03