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HRID 383566생성일: 2026년 10월 26일

Hydrochloric Acid → N-(1-(2,4-difluorophenyl)-1H-pyrazol-5-yl)acetamide

https://huagongshe.com/reaction/383566

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물Potassium HydroxideHCID 14797—
반응물1-(2,4-Difluorophenyl)-1H-pyrazol-5-amineHCID 43316768—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매1,2-DichloroethaneHCID 11—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
용매DichloromethaneHCID 6344—
생성물N-(1-(2,4-difluorophenyl)-1H-pyrazol-5-yl)acetamideHCID 67199804—

반응 조건

온도80 °C

반응 단계

A solution of 1-(2,4-difluorophenyl)-1H-pyrazol-5-amine (5.00 g, 26 mmol), in 80 mL of 1,2-DCE was added DMAP (0.94 g, 7.7 mmol), Ac2O (12 mL, 128 mmol) and Et3N (18 mL, 128 mmol). The dark brown reaction mixture was heated at 80° C. in an oil bath for 18 h. After cooling to RT, it was diluted with 20 mL of DCM and washed with saturated aqueous solution of sodium bicarbonate, and brine. The resulting organic solution was then dried over magnesium sulfate and concentrated under reduced pressure to give viscous brown oil which contains the bis-acylated product along with residual amount of Ac2O and AcOH. The viscous brown oil was dissolved in 50 mL of EtOH and treated with KOH (5.0 g 129 mmol). After the reaction mixture was stirred at RT for 4 h, it was acidified with 2 N HCl to pH 4. The volatile portion was removed on the rotovap. The residue was diluted with 150 mL of EtOAc, washed with saturated aqueous solution of sodium bicarbonate, and brine. The resulting organic solution was then dried over magnesium sulfate and concentrated under reduced pressure. Purification of the crude material on an ISCO 80 g column (60-100% EtOAc in hexanes) afforded N-(1-(2,4-difluorophenyl)-1H-pyrazol-5-yl)acetamide as an off-white solid. MS (ES+): 238.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367671B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-e76ac1841d114f8aabc2b15d1f452ecb
출처 메모uspto-grants-2013_02