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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16845생성일: 2026년 10월 25일

Cesium carbonate → Ethyl 5-(4-methyl-1,4-diazepan-1-yl)thiophene-2-carboxylate

https://huagongshe.com/reaction/16845

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1-MethylhomopiperazineHCID 228349—
반응물Ethyl 5-bromothiophene-2-carboxylateHCID 605723—
반응물Binap, (A+-)-HCID 634876—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물Ethyl 5-(4-methyl-1,4-diazepan-1-yl)thiophene-2-carboxylateHCID 6658979312.7%

반응 조건

온도80 °C

반응 단계

Palladium(II)acetate (0.135 g, 0.60 mmol) was added to ethyl 5-bromothiophene-2-carboxylate (1.411 g, 6 mmol), 1-methyl-1,4-diazepane (0.822 g, 7.20 mmol), BINAP (0.374 g, 0.60 mmol) and cesium carbonate (2.74 g, 8.40 mmol) in dioxane (40 mL) warmed to 80° C. for 18 h under nitrogen. The crude reaction mixture was purified by ion exchange chromatography, using a SCX column. The desired product was eluted from the column using 7M NH3/MeOH. Fractions were evaporated to dryness to afford the crude product. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 5% 3M ammonia/MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 5-(4-methyl-1,4-diazepan-1-yl)thiophene-2-carboxylate (0.204 g, 12.67%) as a yellow gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737149B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0491bb1be2c3466bae7581723a930f93
출처 메모uspto-grants-2010_06