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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74160생성일: 2026년 10월 24일

Ammonia → 5-(Benzothiazol-2-yl)-2-methyl-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/ko/reaction/74160

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물2-AminothiophenolHCID 8713—
반응물2-methyl-1-(tetrahydropyran-4-yl)benzimidazole-5-carboxylic acid HCl saltHCID 67498445—
생성물5-(Benzothiazol-2-yl)-2-methyl-1-(tetrahydropyran-4-yl)benzimidazoleHCID 498213791.9%

반응 조건

온도150 °C

반응 단계

A 4-neck flask (50 mL) equipped with reflux condenser was charged with 2-methyl-1-(tetrahydropyran-4-yl)benzimidazole-5-carboxylic acid HCl salt (see Working Example 4-3) (0.28 g, 1.08 mmol), 2-aminobenzenethiol (0.14 g, 1.08 mmol) and polyphosphoric acid (approx. 11 g), and this was heated to 150° C. and stirred for 17 hours. After being allowed to cool to room temperature, this was cooled in ice (0 to 5° C.), and concentrated aqueous ammonia (28%) was added to the liquid to give approx. pH 9. After distilling off the solvent under reduced pressure, the brown viscous residue was extracted with ethyl acetate, this was dried over anhydrous magnesium sulfate. The residue obtained after again distilling off the solvent under reduced pressure was purified by PTLC to yield the title compound (0.007 g, 1.8% yield) as greenish-pale yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2a6d9b5436cc47f0a047a04680d0c6ab
출처 메모uspto-grants-2014_09