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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533647생성일: 2026년 10월 25일

1-Hydroxybenzotriazole → 2-(2-ethylsulfanyl-phenyl)-3-methyl-6-trifluoromethyl-3H-benzimidazole-4-ylamine

https://huagongshe.com/reaction/533647

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물2-(Ethylsulfanyl)benzoic acidHCID 425758—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물N'-methyl-5-trifluoromethyl-benzene-1,2,3-triamineHCID 68091212—
용매WaterHCID 962—
용매PyridineHCID 1049—
생성물2-(2-ethylsulfanyl-phenyl)-3-methyl-6-trifluoromethyl-3H-benzimidazole-4-ylamineHCID 6798168715.2%

반응 단계

To a mixture of N′-methyl-5-trifluoromethyl-benzene-1,2,3-triamine (1.3 g), 2-ethylsulfanylbenzoic acid (1.3 g), and pyridine (12 mL), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.4 g) and 1-hydroxybenzotriazole (86 mg) were added at room temperature. The mixture was stirred at room temperature for 5 hours, then heated to 110° C., and stirred with heating for 8 hours. After the reaction mixture was allowed to cool to room temperature, the reaction mixture was diluted with water, and extracted with ethyl acetate. The combined organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 339 mg of 2-(2-ethylsulfanyl-phenyl)-3-methyl-6-trifluoromethyl-3H-benzimidazole-4-ylamine (hereinafter, Present Compound 336).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853238B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-0cbd1663b2d84c7797cd713e2e24c962
출처 메모uspto-grants-2014_10