Acetic Acid → 3-Chloro-4,6-dimethylpyridazine

HRID 885946노트

반응식

HRID 885946 반응식
[Cl:1][C:2]1[N:3]=[N:4][C:5]([CH3:8])=[CH:6][CH:7]=1.[C:9](O)(=O)C.S(=O)(=O)(O)O.S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+].[OH-].[NH4+]>O.[N+]([O-])([O-])=O.[Ag+]>[Cl:1][C:2]1[N:3]=[N:4][C:5]([CH3:8])=[CH:6][C:7]=1[CH3:9]

참가 물질

8

실험 절차

To a mixture of 3-chloro-6-methylpyridazine (0.2 g, 1.55 mmol), acetic acid (0.2 mL, 3.49 mmol), sulphuric acid (0.124 mL, 2.33 mmol) and silver nitrate (0.026 g, 0.16 mmol) in water (4.5 mL) was added dropwise a solution of ammonium persulfate in water (1.5 mL). The mixture was held at 75° C. for 30 minutes, allowed to cool to r.t. and poured onto ice. The mixture was basified to pH 9-10 with ammonium hydroxide and extracted with DCM (50 mL). The organic fraction was washed with aqueous sodium hydroxide (1.0N, 2×15 mL), dried (MgSO4), concentrated in vacuo and purified by preparative HPLC (Method 6). The product was dissolved in DCM (15 mL), washed with aqueous potassium carbonate solution (0.7M) and concentrated in vacuo to give the title compound (0.111 g, 50%) as a pink solid. δH (DMSO-d6) 7.62 (1H, s), 2.57-2.54 (3H, m), 2.33 (3H, s). LCMS (ES+) 142.97 (M+H)+, RT 1.93 minutes (Method 1).

후처리

  1. additionpoured onto ice
  2. extractionextracted with DCM (50 mL)
  3. washThe organic fraction was washed with aqueous sodium hydroxide (1.0N, 2×15 mL)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. custompurified by preparative HPLC (Method 6)
  7. dissolutionThe product was dissolved in DCM (15 mL)
  8. washwashed with aqueous potassium carbonate solution (0.7M)
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-66b6ede1da874660a94383ed581912e5
출처 데이터셋
uspto-grants-2012_08
특허 번호
US08242116B2

반응 노트

불러오는 중…