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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251659생성일: 2026년 10월 26일

Triethylamine → 5-(5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamido)-pentanoic acid methyl ester

https://huagongshe.com/reaction/251659

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물Methyl 5-aminopentanoate hydrochlorideHCID 13672034—
반응물5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acidHCID 136387942—
반응물HCID 178418300HCID 178418300—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물5-(5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamido)-pentanoic acid methyl esterHCID 13638794668%

반응 단계

5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (328 mg, 1 mmol) and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (394 mg, 2 mmol), hydroxybenzo-triazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and 5-aminovaleric acid methyl ester hydrochloride (202 mg, 1.2 mmol) were added. The mixture was stirred for 24 hours at room temperature. The mixture was diluted with 400 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (300mg, 68% yield) as a red solid. LC-MS (m/z) 442 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863315B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-8f3ee56e301a4dd28d0a755650db4b20
출처 메모uspto-grants-2011_01