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HRID 1842740作成日:2026年10月25日

(3R)-(+)-3-(Dimethylamino)pyrrolidine → N-{4-[(3R)-3-dimethylaminopyrrolidin-1-yl]-2-methoxy-5-nitrophenyl}-5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-amine

https://huagongshe.com/reaction/1842740

反応式

関与物質

役割名称HCID仕込み量
反応物(3R)-(+)-3-(Dimethylamino)pyrrolidineHCID 2758521—
反応物N-(4-fluoro-2-methoxy-5-nitrophenyl)-5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-amineHCID 71239199—
溶媒DimethylacetamideHCID 31374—
生成物N-{4-[(3R)-3-dimethylaminopyrrolidin-1-yl]-2-methoxy-5-nitrophenyl}-5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-amineHCID 7126990465%

反応条件

温度140 °C

反応手順

(3R)—N,N-dimethylpyrrolidin-3-amine (255 mg, 2.24 mmol) was added to a suspension of N-(4-fluoro-2-methoxy-5-nitrophenyl)-5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-amine (Intermediate 79, 414 mg, 1.02 mmol) in DMA (4 mL) and the mixture was heated in a microwave at 140° C. for 0.5 h. The mixture was then concentrated in vacuo and the residue was dissolved in EtOAc (50 mL). Purification by ion exchange chromatography, using an SCX column and eluting with 0.35M methanolic ammonia provided semi-purified material after concentration of appropriate fractions in vacuo. Purification by FCC, eluting with 1-8% CH3OH in CH2Cl2 gave the title compound (330 mg, 65%) as an orange dry film; 1H NMR: 1.75-1.86 (1H, m), 2.13-2.19 (1H, m), 2.21 (6H, s), 2.37 (3H, s), 2.75 (1H, s), 3.10-3.20 (2H, m), 3.21-3.27 (1H, m), 3.46 (1H, td), 3.90 (3H, s), 3.94 (3H, s), 6.56 (1H, s), 7.03 (1H, t), 7.21-7.26 (1H, m), 7.49 (1H, d), 7.94 (1H, s), 8.05 (1H, s), 8.23 (1H, s), 8.37 (1H, d), 8.39 (1H, s); m/z: ES+ MH+ 502.33.

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-0ba3a640dd814c2d85a8fc7976e36872
出典メモuspto-grants-2015_02