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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1826795생성일: 2026년 10월 25일

Hydrochloric Acid → 5-(3-{4-Ethoxycarbonyl-5-methyl-3-[3-(4-methylpiperazin-1-yl)-propyl]-1H-pyrrol-2-ylmethylene}-2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic Acid

https://huagongshe.com/reaction/1826795

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PiperidineHCID 8082—
반응물5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acidHCID 22135397—
반응물5-formyl-2-methyl-4-[3-(4-methylpiperazin-1-yl)propyl]-1H-pyrrole-3-carboxylic acid ethyl esterHCID 58779587—
용매EthanolHCID 702—
생성물5-(3-{4-Ethoxycarbonyl-5-methyl-3-[3-(4-methylpiperazin-1-yl)-propyl]-1H-pyrrol-2-ylmethylene}-2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic AcidHCID 69584084—

반응 조건

온도60 °C

반응 단계

A mixture of 5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acid (51 mg, 0.2 mmol), 5-formyl-2-methyl-4-[3-(4-methyl-piperazin-1-yl)-propyl]-1H-pyrrole-3-carboxylic acid ethyl ester (64 mg, 0.2 mmol) and piperidine (0.2 mL) in ethanol (1 mL) was heated in a sealed tube at 60° C. for 5 hours. The reaction was acidified with 1N HCl and the resulted precipitate was collected by vacuum filtration, washed with water and dried to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07053086B2
출처 데이터셋uspto-grants-2006_05
ORD IDord-6e6f8ec4045349cfb1878a25bc087a52
출처 메모uspto-grants-2006_05