Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1744592생성일: 2026년 10월 25일
Potassium Carbonate → N-{3-Cyano-4-[4-(2-hydroxyethyl)piperazin-1-yl]phenyl}-1-(4-fluorophenyl)pyrrole-2-carboxamide
https://huagongshe.com/reaction/1744592
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| 반응물 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 반응물 | 1-(4-fluorophenyl)-1H-pyrrole-2-carboxylic acid | HCID 17390044 | — |
| 반응물 | 5-Amino-2-[4-(2-hydroxyethyl)piperazin-1-yl]benzonitrile | HCID 17609593 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-{3-Cyano-4-[4-(2-hydroxyethyl)piperazin-1-yl]phenyl}-1-(4-fluorophenyl)pyrrole-2-carboxamide | HCID 22228195 | 35.5% |
반응 단계
1-(4-Fluorophenyl)pyrrole-2-carboxylic acid (2 g), 5-amino-2-[4-(2-hydroxyethyl)piperazin-1-yl]benzonitrile (2.4 g), 1-hydroxybenzotriazole (1.8 g) and 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide (2.2 g) were added to dimethylformamide (25 ml) and the mixture was stirred at room temperature for 5 h. The reaction mixture was treated with aqueous potassium carbonate solution and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (mobile phase:chloroform:methanol=100:1) to give an oily substance. The obtained oily substance was recrystallized from a mixed solvent of toluene-n-hexane to give the title compound (1.5 g), melting point: 170–171° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07015218B1 |
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| 출처 데이터셋 | uspto-grants-2006_03 |
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| ORD ID | ord-390c5e2179a641e698966627071479d8 |
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| 출처 메모 | uspto-grants-2006_03 |
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