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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50004생성일: 2026년 10월 23일

Sodium Hydroxide → N-(2-(diethylamino)ethyl)-5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxamide

https://huagongshe.com/ko/reaction/50004

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물N,N'-DiethylethylenediamineHCID 67105—
반응물5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic AcidHCID 11073792—
반응물HCID 178418300HCID 178418300—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
용매Sodium BicarbonateHCID 516892—
용매Sodium chloride; waterHCID 57417360—
생성물N-(2-(diethylamino)ethyl)-5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxamideHCID 2076178543%

반응 단계

5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (1204 g) and 6020 mL of dimethylformamide were stirred at room temperature while 1-(3-dimethyl-aminopropyl-3-ethylcarbodiimide hydrochloride (2071 g), hydroxybenzotriazole (1460 g), triethylamine (2016 mL) and diethylethylenediamine (1215 mL) were added. The mixture was stirred for 20 hours at room temperature. The mixture was diluted with 3000 mL of water, 2000 mL of brine and 3000 mL of saturated sodium bicarbonate solution and the pH adjusted to greater than 10 with 10 N sodium hydroxide. The mixture was extracted twice with 5000 mL each time of 10% methanol in dichloromethane and the extracts combined, dried over anhydrous magnesium sulfate and rotary evaporated to dryness. The mixture was with diluted with 1950 mL of toluene and rotary evaporated again to dryness. The residue was triturated with 3:1 hexane:diethyl ether (4000 mL). The solids were collected by vacuum filtration, washed twice with 400 mL of ethyl acetate and dried under vacuum at 34° C. for 21 hours to give 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-diethylamino-ethyl)-amide (819 g, 43% yield) as a light brown solid. 1H-NMR (dimethylsulfoxide-d6) δ0.96 (t, 6H, 2×CH3), 2.31, 2.38 (2×s, 2×CH3), 2.51 (m, 6H 3×CH2), 3.28 (m, 2H, CH2), 7.34 (m, 1H, amide NH), 9.56 (s, 1H, CHO), 11.86 (s, 1H, pyrrole NH). MS m/z 266 [M+1].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710067B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-4280e8a1072d4ca989f211bca84eef5e
출처 메모uspto-grants-2004_03