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HRID 253703作成日:2026年10月25日

Water → (5-Fluoro-1H-indazol-3-yl)-[6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]amine

https://huagongshe.com/reaction/253703

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium BicarbonateHCID 516892—
反応物5-fluoro-1H-indazol-3-amineHCID 4327896—
反応物4-Chloro-6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidineHCID 21939271—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物(5-Fluoro-1H-indazol-3-yl)-[6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidin-4-yl]amineHCID 1038552256.5%

反応条件

温度165 °C

反応手順

A mixture of 4-chloro-6-methyl-2-(2-trifluoromethyl-phenyl)-pyrimidine (0.10 g, 0.37 mmol) and 5-fluoro-1H-indazole-3-ylamine (0.072 g, 0.48 mmol) was heated neat at 160-170° C. for 8 hours. The resulting residue was cooled to ambient temperature then dissolved in N-methyl-pyrrolidinone (2 mL). This mixture was poured into water (20 mL) and sodium bicarbonate (5 mL) was added and the resulting mixture filtered, washing with water. Purification by preparative HPLC provided the title compound (0.081 g, 43% yield) as a tan solid. 1H-NMR (500 MHz, DMSO-d6) δ 12.8 (br s, 1H), 10.6 (br s, 1H), 7.86 (d, J=8.0 Hz, 1H), 7.77 (m, 4H), 7.62 (br s, 1H), 7.50 (m, 1H), 7.29 (m, 1H), 2.44 (s, 3H) ppm; LC-MS 388.05 (M+H); Rt (Method A) 2.900 minutes.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872129B2
出典データセットuspto-grants-2011_01
ORD IDord-9502545c17784914b5a2cfe4a1d4e8bc
出典メモuspto-grants-2011_01