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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1842737생성일: 2026년 10월 27일

Methanol → N1-(2-dimethylaminoethyl)-5-methoxy-N1-methyl-N4-[5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-yl]benzene-1,2,4-triamine

https://huagongshe.com/reaction/1842737

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물DichloromethaneHCID 6344—
반응물Ammonium ChlorideHCID 25517—
반응물N'-(2-Dimethylaminoethyl)-2-methoxy-N'-methyl-N-[5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-yl]-5-nitrobenzene-1,4-diamineHCID 71270206—
촉매IronHCID 23925—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물N1-(2-dimethylaminoethyl)-5-methoxy-N1-methyl-N4-[5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-yl]benzene-1,2,4-triamineHCID 8667725478%

반응 단계

A mixture of N′-(2-dimethylaminoethyl)-2-methoxy-N′-methyl-N-[5-methyl-4-(1-methy-lindol-3-yl)pyrimidin-2-yl]-5-nitrobenzene-1,4-diamine (Intermediate 82, 202 mg, 0.41 mmol), iron (138 mg, 2.48 mmol) and NH4Cl (15.45 mg, 0.29 mmol) in ethanol (16 mL) and water (5.33 mL) was heated at reflux for 3 h. The mixture was then cooled and concentrated in vacuo to give a thick slurry. CH2Cl2 (100 mL) and CH3OH (10 mL) was then added and the mixture was stirred for 0.25 h and then filtered. The filter cake was washed further with CH2Cl2 and CH3OH and the combined organics were dried (MgSO4) and concentrated in vacuo. Purification by FCC, eluting with 1-8% methanolic ammonia in CH2Cl2 gave the title compound (147 mg, 78%) as a yellow dry film; m/z: ES+ MH+ 460.36.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08946235B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-c67e5c78739c47738912c9b710add88c
출처 메모uspto-grants-2015_02