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HRID 1842821作成日:2026年10月24日

1,2-Ethanediamine, N1,N1,N2-trimethyl- → N1-(4-(1H-indol-3-yl)pyrimidin-2-yl)-N4-(2-(dimethylamino)ethyl)-2-methoxy-N4-methyl-5-nitrobenzene-1,4-diamine

https://huagongshe.com/ja/reaction/1842821

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
反応物DiisopropylethylamineHCID 81531—
反応物N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-(1H-indol-3-yl)pyrimidin-2-amineHCID 71240865—
溶媒DimethylacetamideHCID 31374—
生成物N1-(4-(1H-indol-3-yl)pyrimidin-2-yl)-N4-(2-(dimethylamino)ethyl)-2-methoxy-N4-methyl-5-nitrobenzene-1,4-diamineHCID 7124087880.5%

反応条件

温度140 °C

反応手順

N1,N1,N2-Trimethylethane-1,2-diamine (83 mg, 0.82 mmol) was added to a mixture of N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-(1H-indol-3-yl)pyrimidin-2-amine (Intermediate 68, 409 mg, 0.74 mmol), DIPEA (0.259 mL, 1.48 mmol) and DMA (3 mL). The resulting mixture was heated in a microwave at 140° C. for 0.5 h. Part-purification was achieved by ion exchange chromatography, using an SCX column (20 g) and eluting with 0.35 M methanolic ammonia. Appropriate fractions were concentrated in vacuo to provide an orange/brown gum. This gum was triturated with ethanol (15 mL) to give a solid which was collected by filtration and dried under vacuum to give the title compound (275 mg, 80%) as an orange solid; 1H NMR: 2.18 (6H, s), 2.45-2.55 (2H, m), 2.87 (3H, s), 3.25-3.30 (2H, m), 3.97 (3H, s), 6.87 (1H, s), 7.08 (1H, t), 7.18 (1H, t), 7.29 (1H, d), 7.46 (1H, d), 8.03 (1H, s), 8.33 (3H, dd), 8.66 (1H, s), 11.80 (1H, s); m/z: ES+ MH+ 462.34.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08946235B2
出典データセットuspto-grants-2015_02
ORD IDord-8bba3d49206841978351172fa97b30c4
出典メモuspto-grants-2015_02