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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1747304생성일: 2026년 10월 27일

Potassium Carbonate → 3-[3-(1,4-Dimethyl-1H-indol-3-ylmethyl)-5,6-dimethyl-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl ester

https://huagongshe.com/reaction/1747304

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물DimethylacetamideHCID 31374—
반응물Ethyl trans-2-hexenoateHCID 5364778—
반응물1-(1,4-Dimethyl-1H-indol-3-ylmethyl)-5,6-dimethyl-1,3-dihydro-benzimidazol-2-oneHCID 59497421—
용매Ethyl AcetateHCID 8857—
생성물3-[3-(1,4-Dimethyl-1H-indol-3-ylmethyl)-5,6-dimethyl-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl esterHCID 59497668—

반응 조건

온도130 °C

반응 단계

A mixture of 1-(1,4-Dimethyl-1H-indol-3-ylmethyl)-5,6-dimethyl-1,3-dihydro-benzimidazol-2-one (0.1 g, 0.31 mmol), K2CO3 (87 mg, 0.63 mmol) and ethyl trans-2-hexenoate (0.45 g, 3.1 mmol) was heated to 130° C. for 20 min in a microwave. Since the starting material was not soluble in ethyl trans-2-hexenoate even after heating, DMA (2 mL) was added to the reaction mixture and heated again at 150° C. for 30 min. Although the un-reacted starting material was present, the reaction mixture was diluted with ethyl acetate and washed with water (×4). The organic phase was dried over Na2SO4 and concentrated. The resulting heterogeneous residue was purified by silica gel prep TLC using 4:1 hexanes:ethyl acetate as an eluent to afford 25 mg of the desired product as an oil. LCMS (ESMS): m/z 462.88 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09150556B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-070016990bc84c339ee2f55ce7a48bd0
출처 메모uspto-grants-2015_10