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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244901생성일: 2026년 10월 26일

Dibutyltin dichloride → 5-(3,3-Dimethyl-but-1-ynyl)-3-(4-[1,2,3]triazol-1-yl-cyclohexylamino)-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/244901

반응식

참여 물질

역할이름HCID투입량
반응물Dibutyltin dichlorideHCID 12688—
반응물PhenylsilaneHCID 12752—
반응물Methyl 3-amino-5-(3,3-dimethylbut-1-yn-1-yl)thiophene-2-carboxylateHCID 24989346—
반응물4-(1H-1,2,3-triazol-1-yl)cyclohexan-1-oneHCID 57424092—
용매TetrahydrofuranHCID 8028—
생성물5-(3,3-Dimethyl-but-1-ynyl)-3-(4-[1,2,3]triazol-1-yl-cyclohexylamino)-thiophene-2-carboxylic acid methyl esterHCID 24988980—

반응 단계

To a solution of 3-amino-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester (example 9) (0.387 g, 1.6 mmol) and 4-[1,2,3]triazol-1-yl-cyclohexanone (0.27 g, 1.6 mmol) in dry THF is added dibutyltin dichloride (0.024 g, 0.080 mmol) followed by phenylsilane (0.276 ml, 2.2 mmol). The mixture is stirred overnight at room temperature. Solvent is evaporated under reduced pressure, and the residue is diluted with ethyl acetate. The organic layer is washed with water and brine, dried with sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel using gradient 50-100% ethyl acetate in hexane to afford 5-(3,3-dimethyl-but-1-ynyl)-3-(4-[1,2,3]triazol-1-yl-cyclohexylamino)-thiophene-2-carboxylic acid methyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658674B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-0450caac0f384b8ca39dbf52f6ee1933
출처 메모uspto-grants-2014_02