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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1874396생성일: 2026년 10월 24일

p-Toluenesulfonic acid monohydrate → N-[3-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide p-toluenesulfonate

https://huagongshe.com/ko/reaction/1874396

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참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물N-[3-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 25127854—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
생성물N-[3-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide p-toluenesulfonateHCID 8663197567.2%

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온도0 °C

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To a solution of N-[3-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-a]pyridin-6-yl}oxy)phenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide (204 mg, 0.474 mmol) in ethanol (8 mL) was added a solution of p-toluenesulfonic acid monohydrate (94.7 mg, 0.498 mmol) in ethyl acetate (1.10 mL), and the mixture was stirred at 0° C. for 2 hr and at room temperature for 2 days. The precipitated solid was collected by filtration and washed with ethanol to give the title compound (192 mg, 67%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304557B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-03a8fbf0bfba4b0bb725282d08c13a5b
출처 메모uspto-grants-2012_11