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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ethyl 5-(chloromethyl)-2-furancarboxylate | HCID 263166 | — |
| 반응물 | 2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazole | HCID 14012845 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | ethyl 5-[[2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazol-1-yl]methyl]-2-furancarboxylate | HCID 19734408 | 86.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05272150 |
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| 출처 데이터셋 | uspto-grants-1993_12 |
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| ORD ID | ord-788b481de1f94d69a8e058708303766f |
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| 출처 메모 | uspto-grants-1993_12 |
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