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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12285생성일: 2026년 10월 23일

6-Thiophen-3-yl-2-(2-trimethylsilanylethoxymethyl)-4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzimidazol-2-yl]-2H-pyridazin-3-one → 4-(1H-Benzimidazol-2-yl)-6-thiophen-3-yl-2H-pyridazin-3-one

https://huagongshe.com/ko/reaction/12285

반응식

참여 물질

역할이름HCID투입량
반응물6-Thiophen-3-yl-2-(2-trimethylsilanylethoxymethyl)-4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzimidazol-2-yl]-2H-pyridazin-3-oneHCID 68680227—
용매DichloromethaneHCID 6344—
용매Trifluoroacetic acidHCID 6422—
용매1,1-EthanedithiolHCID 33645—
생성물4-(1H-Benzimidazol-2-yl)-6-thiophen-3-yl-2H-pyridazin-3-oneHCID 135978788—

반응 단계

30 mg of 6-thiophen-3-yl-2-(2-trimethylsilanylethoxymethyl)-4-[1-(2-trimethylsilanyl -ethoxymethyl)-1H-benzimidazol-2-yl]-2H-pyridazin-3-one is dissolved in a mixture of dichloromethane (1 ml) and trifluoroacetic acid (1 ml), 18 μl of ethanedithiol are added, and the resulting solution is stirred at room temperature for 18 hours. After the solvent has been distilled off, the crude product is purified by preparative RP-HPLC (0-100% acetonitrile (+0.05% formic acid) in water (+0.05% formic acid)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727989B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a0bb0e36af1c4605afc2d9a01c94eb29
출처 메모uspto-grants-2010_06