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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19494생성일: 2026년 10월 24일

Methanesulfonic Acid → N-[3-(1H-Imidazol-2-ylamino)-4-methyl-phenyl]-3-trifluoromethyl-benzamide

https://huagongshe.com/ko/reaction/19494

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물m-(Trifluoromethyl)benzamideHCID 74535—
반응물N-(2,2-diethoxyethyl)carbodiimideHCID 10749464—
용매EthanolHCID 702—
생성물N-[3-(1H-Imidazol-2-ylamino)-4-methyl-phenyl]-3-trifluoromethyl-benzamideHCID 58973096—

반응 단계

A mixture of N-(2,2-diethoxyethyl)carbodiimide (398 mg, 2.51 mmol), 3-amino-4-methyl-phenyl]-3-trifluoromethyl-benzamide (649 mg, 2.20 mmol), methanesulfonic acid (143 μL, 2.20 mmol) in ethanol (25 mL) is heated at reflux for 16 hours. An additional portion of N-(2,2-diethoxyethyl)carbodiimide (525 mg, 3.32 mmol) and methanesulfonic acid (143 μL, 2.20 mmol) are added. After an additional 3 hours refluxing, the reaction mixture is concentrated. The residue is dissolved in HCl (6N, 5 mL) and ethanol (5 mL). After stirring overnight, the reaction mixture is concentrated and basified with 25% NaOH solution to a pH of 14. The mixture is stirred for 30 minutes, extracted with CH2Cl2, dried, concentrated and purified by column chromatography (silica gel, eluting with 7N NH3 in methanol:dichloromethane from 2% to 4%) to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745437B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-2b6863eb1d6b4541a5678bf5343bed44
출처 메모uspto-grants-2010_06