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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74216생성일: 2026년 10월 23일

Water → 5-(2-Hydroxy-4-nitroanilinocarbonyl)-2-methyl-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/ko/reaction/74216

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물2-Amino-4-NitrophenolHCID 3613389—
반응물2-methyl-1-(tetrahydropyran-4-yl)benzimidazole-5-carboxylic acid HCl saltHCID 67498445—
촉매DimethylformamideHCID 6228—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물5-(2-Hydroxy-4-nitroanilinocarbonyl)-2-methyl-1-(tetrahydropyran-4-yl)benzimidazoleHCID 6749817717.1%

반응 단계

To a suspension of 2-methyl-1-(tetrahydropyran-4-yl)benzimidazole-5-carboxylic acid HCl salt (see Working Example 4-3) (0.75 g, 2.9 mmol) in toluene (10 mL) containing DMF (1 drop) was added thionyl chloride (0.41 g, 3.4 mmol), and this was refluxed for 7 hours with stirring. After the reaction was complete, concentration at reduced pressure gave a residue that was added to 2-hydroxy-5-nitroaniline (0.44 g, 2.9 mmol), triethylamine (0.32 g, 3.2 mmol) and tetrahydrofuran (5 mL), and this was stirred at room temperature for 3 hours. After the reaction was complete, water (30 mL) was added and the precipitated crystals were filtered off. After the crystals were washed with water, they were dried with heating at reduced pressure to yield the title compound (195 mg, 17.1%) as a light brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0d156a25ad514904a3cdcd09accb1945
출처 메모uspto-grants-2014_09