Reaktion #1929076

ord-51bcd14a542d448faba46498477e1e5b

Reaktionsgleichung

Cl
hydrogen chloride
CC(C)(C)[O-].[K+]
potassium tert-butoxide
COC(=O)C1(NC(=O)Cc2cc(Br)ccc2C)CCCCC1
compound
COC(=O)C1(NC(=O)Cc2cc(Br)ccc2C)CCCCC1
Methyl 1-{[(5-bromo-2-methylphenyl)acetyl]amino}cyclohexanecarboxylate
O
water
Cc1ccc(Br)cc1C1=C(O)C2(CCCCC2)NC1=O
3-(5-Bromo-2-methylphenyl)-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-one

Lösungsmittel

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter cooling
  2. 2
    FiltrationThe precipitate was filtered off with suction
  3. 3
    Waschenwashed with water
  4. 4
    Sonstigedried

Vorschrift

1.71 g (15.2 mmol) of potassium tert-butoxide were added to 2.80 g (7.60 mmol) of the compound from Example 12A in 15 ml of N,N-dimethylformamide. The reaction mixture was heated at 80° C. for 15 minutes. After cooling, water was added and aqueous hydrogen chloride solution was added dropwise. The precipitate was filtered off with suction, washed with water and dried. This gave 2.33 g (90% of theory) of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08946124B2uspto-grants-2015_02