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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1070431생성일: 2026년 10월 27일

Pyrrole-2-carboxaldehyde → Methyl 2-[(2-formyl-1H-pyrrol-1-yl)methyl]pyridine-3-carboxylate

https://huagongshe.com/reaction/1070431

반응식

참여 물질

역할이름HCID투입량
반응물Pyrrole-2-carboxaldehydeHCID 13854—
반응물Sodium hydrideHCID 24758—
반응물Methyl 2-(chloromethyl)pyridine-3-carboxylateHCID 19081344—
용매DimethylformamideHCID 6228—
생성물Methyl 2-[(2-formyl-1H-pyrrol-1-yl)methyl]pyridine-3-carboxylateHCID 53438888—

반응 단계

To a suspension of sodium hydride (5.8 g, 0.12 mol), in dry N,N-dimethyl formamide (25 mL) was added slowly under nitrogen a solution of pyrrole 2-carboxaldehyde (10.5 g, 0.11 mol) in N,N-dimethylformamide (10 mL), and the reaction mixture was stirred at room temperature for 30 minutes. The reaction was then cooled to 5° C. and 2-chloromethyl-pyridine-3-carboxylic acid methyl ester of Step A was added slowly, the temperature being maintained at or below 20° C. After the addition was complete, the reaction was stirred at room temperature for 30 minutes. The mixture was evaporated to dryness, and the residue was dissolved in ethyl acetate (250 mL). This solution was washed with water and dried over anhydrous magnesium sulfate. The solvent was then removed in vacuo leaving a dark crystalline solid (23.4 g), which was purified by chromatography on silica gel eluting with a gradient of ethyl acetate/petroleum ether to provide the title compound as a tan crystalline solid (13.75 g), m.p. 91-93° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06903091B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-662d44bfb8db4d6eb0b0c73fecd7464d
출처 메모uspto-grants-2005_06