반응 #8089

ord-91f9a9d242cc4d829d962d9a6373321d

반응 방정식

O=C([O-])O.[Na+]
sodium hydrogencarbonate
COC(=O)c1cc(-c2ccc(SC)cc2)n[nH]c1=O
4-methoxycarbonyl-6-[4-(methylthio)-phenyl]-2H-pyridazin-3-one
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)CBr
isobutyl bromide
CSc1ccc(-c2cc(C(=O)O)c(=O)n(CC(C)C)n2)cc1
title compound
수율 65.1%
CSc1ccc(-c2cc(C(=O)O)c(=O)n(CC(C)C)n2)cc1
4-carboxy-2-isobutyl-6-[4-(methylthio)-phenyl]-2H-pyridazin-3-one
수율 65.1%

반응 조건

온도
80°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to drop back to room temperature
  2. 2
    추출The mixture was then extracted with ethyl acetate
  3. 3
    세척The extract was washed with brine
  4. 4
    건조dried over anhydrous sodium sulfate
  5. 5
    workup.DISTILLATIONThe solvent was distilled off
  6. 6
    기타the residue was reacted

실험 절차

To a solution of 4-methoxycarbonyl-6-[4-(methylthio)-phenyl]-2H-pyridazin-3-one (8.00 g, 29.0 mmol) in N,N-dimethylformamide (80 mL) were added potassium carbonate (8.02 g, 58.0 mmol) and isobutyl bromide (4.76 g, 34.8 mmol), and the mixture was stirred at 80° C. for 2 hours. The temperature of the reaction mixture was allowed to drop back to room temperature, and a saturated aqueous solution of sodium hydrogencarbonate was added. The mixture was then extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was distilled off. Following the procedure of Example 1 (7), the residue was reacted to yield the title compound as a yellow solid [yield: 65.1% (2 steps)].

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087606B2uspto-grants-2006_08