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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226335생성일: 2026년 10월 26일

1-Hydroxybenzotriazole → ethyl (2E)-3-[6-({1-[4-(1H-pyrrol-1-yl)benzoyl]-4-piperidyl}amino)-3-pyridyl]acrylate

https://huagongshe.com/reaction/226335

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-(1H-Pyrrol-1-yl)benzoic acidHCID 2737256—
반응물ethyl (2E)-3-[6-(4-piperidylamino)-3-pyridyl]acrylate dihydrochlorideHCID 86603643—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물ethyl (2E)-3-[6-({1-[4-(1H-pyrrol-1-yl)benzoyl]-4-piperidyl}amino)-3-pyridyl]acrylateHCID 86603647107.5%

반응 조건

온도23 °C

반응 단계

To a suspension of ethyl (2E)-3-[6-(4-piperidylamino)-3-pyridyl]acrylate dihydrochloride (500 mg) in DMF (5 ml) was added 4-(1H-pyrrol-1-yl)benzoic acid (309 mg), EDCI.HCl (317 mg), HOBt (223 mg), Et3N(0.63 ml), the mixture was stirred at 23° C. for 8 hours. The mixed solution was poured into a mixture of water (20 ml) and AcOEt (20 ml). The organic layer was separated, washed with water twice and brine, dried-over sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluted with 5% MeOH in dichloromethane to give ethyl (2E)-3-[6-({1-[4-(1H-pyrrol-1-yl)benzoyl]-4-piperidyl}amino)-3-pyridyl]acrylate (686 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557127B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-e59c90f992f942e79eaf2fc990c3f4ce
출처 메모uspto-grants-2009_07