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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1045911생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1045911

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Potassium AcetateHCID 517044—
반응물1,3-dimethyl-1H-pyrazol-4-amine hydrochlorideHCID 12687197—
용매Ethyl AcetateHCID 8857—
생성물N-(1,3-dimethylpyrazol-4-yl)acetamideHCID 19346285—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569298B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-b2f475017a2c4b4eb7a6aa1e4d87a5c4
출처 메모uspto-grants-2013_10