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HRID 747098作成日:2026年10月26日

Water → 5-chloro-6-(2,4,6-trifluorophenyl)-N-[(1S)-2,2,2-trifluoro-1-methylethyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amine

https://huagongshe.com/reaction/747098

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物(S)-1,1,1-trifluoropropan-2-amineHCID 10964447—
反応物5,7-Dichloro-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidineHCID 11045387—
溶媒DimethylformamideHCID 6228—
生成物5-chloro-6-(2,4,6-trifluorophenyl)-N-[(1S)-2,2,2-trifluoro-1-methylethyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amineHCID 11975043—

反応条件

温度0 °C

反応手順

To a solution of 5,7-dichloro-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]-pyrimidine (200 g, 0.627 mol) in anhydrous DMF (1000 mL) is added (S)-2,2,2-trifluoro-1-methyl-ethylamine (177 g, 1.57 mol). The solution is stirred from about 20° C. to about 30° C. for 24 h. The reaction mixture is added to cold water (3000 mL) slowly over 30 min. The mixture is stirred for 30 min at 10-20° C. The solid product is filtered and washed with water (2×500 mL). The crude product is dissolved into IPA (1000 mL) at 50° C. Water (2000 mL) is added to precipitate the product over 30 min. The mixture is cooled to 0° C. over 1 h and stirred for 1 h at this temperature. The solid is filtered and dried at 65° C./10 mmHg for 20 h to give a light yellow solid (204 g, 82%, 98% HPLC area purity and 99% ee).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07396835B2
出典データセットuspto-grants-2008_07
ORD IDord-835e75ffab714e31a6e73f2eec853a59
出典メモuspto-grants-2008_07