돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16797생성일: 2026년 10월 25일

Cesium carbonate → Ethyl 5-(3,4-dimethylpiperazin-1-yl)thiophene-2-carboxylate

https://huagongshe.com/reaction/16797

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물DimethylpiperazineHCID 198037—
반응물Ethyl 5-bromothiophene-2-carboxylateHCID 605723—
반응물Binap, (A+-)-HCID 634876—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
생성물Ethyl 5-(3,4-dimethylpiperazin-1-yl)thiophene-2-carboxylateHCID 5744041247.7%

반응 조건

온도110 °C

반응 단계

Palladium(II) acetate (0.112 g, 0.50 mmol) was added to a mixture of ethyl 5-bromothiophene-2-carboxylate (0.571 g, 5 mmol), 1,2-dimethyl-piperazine (1.175 g, 5 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.311 g, 0.50 mmol) and cesium carbonate (2.281 g, 7.00 mmol) in toluene (50.0 ml) at 20° C. under nitrogen. The resulting suspension was stirred at 110° C. for 23 h. The crude product was purified by ion exchange chromatography, using a SCX2 column. The crude material was dissolved in methanol and then applied to the column. The desired product was eluted from the column using 2M NH3 in methanol and pure fractions were evaporated to dryness to afford the crude product as a brown oil. This material was further purified by silica column chromatography, eluting with a gradient of 1 to 5% MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 5-(3,4-dimethylpiperazin-1-yl)thiophene-2-carboxylate (0.640 g, 47.7%) as a light brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737149B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c08e5e4b898641779e80d8c5f1544a25
출처 메모uspto-grants-2010_06