Реакция #2195492

ord-9d65452c4aac426e8090702eeda14eeb

Уравнение реакции

Cn1c(=O)oc(=O)c2ccccc21
N-methylisatoic anhydride
Cl
HCl
CCOC(=O)CS(C)(=O)=O
ethylmethanesulfonylacetate
[H-].[Na+]
sodium hydride
[H][H]
hydrogen
Cn1c(=O)c(S(C)(=O)=O)c(O)c2ccccc21
white solids
Выход 48.0%
Cn1c(=O)c(S(C)(=O)=O)c(O)c2ccccc21
4-Hydroxy-3-methanesulfonyl-1-methyl-1H-quinolin-2-one
Выход 48.0%

Растворители

Условия реакции

Температура
90°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураcooled to room temperature
  2. 2
    Температураheated overnight at 120° C
  3. 3
    ТемператураThe mixture was cooled to room temperature
  4. 4
    ДругоеThe solids formed
  5. 5
    Фильтрацияwere filtered
  6. 6
    Промывкаwashed several times by water

Методика

A solution of ethylmethanesulfonylacetate (3.78 g, 22.74 mmol) was added slowly in a suspension of sodium hydride (60% in mineral oil, 1.07 g, 25 mmol) in dimethylacetamide under N2 atmosphere. The mixture was allowed to stir at room temperature until the evolution of hydrogen gas ceased, then heated to 90° C. for 30 min and cooled to room temperature. A solution of N-methylisatoic anhydride (4.43 g, 25 mmol) in dimethylacetamide was added slowly and heated overnight at 120° C. The mixture was cooled to room temperature, poured into ice water and acidified by cold 10% HCl. The solids formed were filtered and washed several times by water to yield 2.76 g (48%) of white solids. Mp 170° C. 1H NMR (DMSO-d6): δ 3.51 (s, 3H), 3.59 (s, 3H), 7.39 (t, J=7.4 Hz, 1H), 7.62 (d, J=8.5 Hz, 1H), 7.84 (t, J=7.0 Hz, 1H), 8.09 (d, J=8.0 Hz, 1H). EIMS m/z 254 (M+1), 276 (M+23). Anal. (C11H11NO4S) C, H, N.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07514225B2uspto-grants-2009_04