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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1842697생성일: 2026년 10월 27일

1,2-Ethanediamine, N1,N1,N2-trimethyl- → N-(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)-N'-(2-dimethylaminoethyl)-2-methoxy-N'-methyl-5-nitrobenzene-1,4-diamine

https://huagongshe.com/reaction/1842697

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
반응물DiisopropylethylamineHCID 81531—
반응물5-chloro-N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amineHCID 71239348—
용매MethanolHCID 887—
용매DimethylacetamideHCID 31374—
생성물N-(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)-N'-(2-dimethylaminoethyl)-2-methoxy-N'-methyl-5-nitrobenzene-1,4-diamineHCID 71270273104%

반응 조건

온도140 °C

반응 단계

N,N,N′-Trimethylethylenediamine (0.188 mL, 1.45 mmol) was added to a mixture of 5-chloro-N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amine (Intermediate 20, 500 mg, 1.21 mmol) and DIPEA (0.250 mL, 1.45 mmol) in DMA (5 mL) and the mixture was heated at 140° C. in a microwave for 0.5 h. The mixture was then diluted with CH3OH and absorbed onto an SCX column. The column was washed with CH3OH and eluted with 1:1 methanolic ammonia in CH2Cl2. Appropriate fractions were concentrated in vacuo to give the title compound (624 mg, 104%) as an orange solid, which was used without further purification; 1H NMR: 2.17 (6H, d), 2.89 (3H, d), 3.87-3.93 (3H, m), 6.84 (1H, s), 7.14 (1H, td), 7.31-7.38 (1H, m), 8.15 (1H, s), 8.39 (1H, d), 8.44 (1H, d), 8.69 (1H, s), 8.85 (1H, d), 8.95 (1H, s); m/z: ES+ MH+ 497.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08946235B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-f2b1eabf42a94f959431ee08bceae2a6
출처 메모uspto-grants-2015_02