Acetic Anhydride → N-(1,3-dimethylpyrazol-4-yl)acetamide

HRID 1045911

반응식

HRID 1045911 반응식
C(O[C:5](=[O:7])[CH3:6])(=O)C.Cl.[CH3:9][N:10]1[CH:14]=[C:13]([NH2:15])[C:12]([CH3:16])=[N:11]1.C([O-])(=O)C.[K+]>CCOC(C)=O>[CH3:9][N:10]1[CH:14]=[C:13]([NH:15][C:5](=[O:7])[CH3:6])[C:12]([CH3:16])=[N:11]1

참가 물질

5

반응물 3

HCID 7918Acetic AnhydrideHCID 517044Potassium AcetateHCID 126871971,3-dimethyl-1H-pyrazol-4-amine hydrochloride

생성물 1

HCID 19346285N-(1,3-dimethylpyrazol-4-yl)acetamide

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

Acetic anhydride (27.2 mL, 243.89 mmol) was dropwise added to a stirred suspension of 1,3-dimethyl-pyrazol-4-amine hydrochloride (12 g, 81.30 mmol) and potassium acetate (7.98 g, 81.30 mmol) in EtOAc (250 mL) at 25° C. The suspension was stirred for 1 hour and the insoluble was removed by filtration. After evaporation of the solvent, the resulting crude material was purified by chromatography on silica gel eluting with 0% to 10% of MeOH in DCM. After evaporation of the solvent, the residue was triturated in Et2O. The resulting precipitate was collected by filtration, washed with Et2O and dried to a constant weight to afford N-(1,3-dimethylpyrazol-4-yl)acetamide. The filtrate was concentrated and purified by flash chromatography on silica gel eluting with 0 to 10% MeOH in DCM. The solvent was evaporated to dryness to afford more N-(1,3-dimethylpyrazol-4-yl)acetamide. The two batches were combined to give N-(1,3-dimethylpyrazol-4-yl)acetamide (6.40 g, 51.4%) as a off-white solid.

후처리

  1. customthe insoluble was removed by filtration
  2. customAfter evaporation of the solvent
  3. customthe resulting crude material was purified by chromatography on silica gel eluting with 0% to 10% of MeOH in DCM
  4. customAfter evaporation of the solvent
  5. customthe residue was triturated in Et2O
  6. filtrationThe resulting precipitate was collected by filtration
  7. washwashed with Et2O
  8. customdried to a constant weight

출처 및 근거

ORD 기록
ord-b2f475017a2c4b4eb7a6aa1e4d87a5c4
출처 데이터셋
uspto-grants-2013_10
특허 번호
US08569298B2

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