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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327028생성일: 2026년 10월 26일

Dimethylformamide → ethyl 5-[[2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazol-1-yl]methyl]-2-furancarboxylate

https://huagongshe.com/reaction/327028

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 5-(chloromethyl)-2-furancarboxylateHCID 263166—
반응물2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazoleHCID 14012845—
용매WaterHCID 962—
생성물ethyl 5-[[2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazol-1-yl]methyl]-2-furancarboxylateHCID 1973440886.7%

반응 단계

To 470 parts of N,N-dimethylformamide were added portionwise 17.3 parts of a dispersion of sodium hydride in mineral oil (50%) and 91.6 parts of 2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazole (as prepared in Example 16 of U.S. Pat. No. 4,695,575) while stirring under a nitrogen atmosphere. After stirring for 1 hour, 67.9 parts of ethyl 5-chloromethyl-2-furancarboxylate were added dropwise while cooling. Stirring was continued for 1 hour and then water was added to the reaction mixture. The product was extracted with methylbenzene and the extract was washed with water, dried, filtered and evaporated. The residue was dried azeotropically with methylbenzene (2x), yielding 119 parts (86.7%) of ethyl 5-[[2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazol-1-yl]methyl]-2-furancarboxylate (interm. 4). Following the same procedure and starting from the appropriate starting materials, there were also prepared:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05272150
출처 데이터셋uspto-grants-1993_12
ORD IDord-788b481de1f94d69a8e058708303766f
출처 메모uspto-grants-1993_12