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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227682생성일: 2026년 10월 24일

2,4-Dimethoxybenzylamine → 2-(2,4-dimethoxybenzylamino)carbonyl-3-(4-nitrophenyl)-1H-pyrrole

https://huagongshe.com/ko/reaction/227682

반응식

참여 물질

역할이름HCID투입량
반응물2,4-DimethoxybenzylamineHCID 597250—
반응물TrimethylaluminumHCID 16682925—
반응물methyl 3-(4-nitrophenyl)-1H-pyrrole-2-carboxylateHCID 18616331—
용매TolueneHCID 1140—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물2-(2,4-dimethoxybenzylamino)carbonyl-3-(4-nitrophenyl)-1H-pyrroleHCID 5775687864.9%

반응 조건

온도20 °C

반응 단계

To 2.435 cm3 (15.84 mmol) of 2,4-dimethoxybenzylamine dissolved in 65 cm3 of toluene are added, at a temperature in the region of 20° C. under an argon atmosphere, 10.3 cm3 (20.59 mmol) of a 2M solution of trimethylaluminium in toluene, followed by addition of 1.95 g (7.92 mmol) of methyl 3-(4-nitrophenyl)-1H-pyrrole-2-carboxylate. After stirring for 1 hour at a temperature in the region of 20° C. and then for 16 hours at a temperature in the region of 60° C., the reaction mixture is diluted with 170 cm3 of ethyl acetate. The resulting solution is washed successively with three times 70 cm3 of saturated aqueous ammonium chloride solution and twice 50 cm3 of water and then dried over anhydrous magnesium sulfate, filtered and concentrated to dryness under reduced pressure (2.7 kPa) to give a yellow solid, which is then stirred in 20 cm3 of acetonitrile at a temperature in the region of 5° C. for 30 minutes. After filtering through a No. 3 sinter funnel, the solid is washed with 10 cm3 of ice-cold acetonitrile and then dried under reduced pressure (2.7 kPa) at a temperature in the region of 35° C. for 3 hours to give 1.96 g of 2-(2,4-dimethoxybenzylamino)carbonyl-3-(4-nitrophenyl)-1H-pyrrole in the form of a yellow solid; ES+: m/z=382: [M+H]+; ES−: m/z=380: [M−H]−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560571B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-e99534bacea84e6baf689b8773f7cf87
출처 메모uspto-grants-2009_07