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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13284생성일: 2026년 10월 24일

Dichloromethane → 2-(6-(4-Methanesulfonyl-phenoxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidine-1-carboxamide

https://huagongshe.com/ko/reaction/13284

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물2-DimethylaminopyridineHCID 21885—
반응물Trimethylsilyl isocyanateHCID 70696—
반응물5-(4-methanesulfonyl-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazoleHCID 23145175—
용매WaterHCID 962—
생성물2-(6-(4-Methanesulfonyl-phenoxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidine-1-carboxamideHCID 11408943—

반응 단계

5 mg of dimethylaminopyridine and 0.029 ml of trimethylsilyl isocyanate were added to a methylene chloride (1 ml) solution of 17.1 mg of 5-(4-methanesulfonyl-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazole obtained in Example 162 (step 7), and the reaction liquid was stirred overnight at room temperature. Water was added to the reaction liquid, and extracted with ethyl acetate, and then washed with saturated saline. After dried and concentrated, the resulting residue was purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid], and the resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7819c548dc1b40ea81bc958cbf8fcd01
출처 메모uspto-grants-2010_06