Реакция #1929076

ord-51bcd14a542d448faba46498477e1e5b

Уравнение реакции

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

Растворители

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураAfter cooling
  2. 2
    ФильтрацияThe precipitate was filtered off with suction
  3. 3
    Промывкаwashed with water
  4. 4
    Другоеdried

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08946124B2uspto-grants-2015_02