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HRID 18110作成日:2026年10月25日

Toluene → 1-[5-(4-Fluoro phenyl)-2-methyl-thiazol-4-yl]-1-{(S)-2-[(5-trifluoromethyl-pyrimidin-2-ylamino)-methyl]-pyrrolidin-1-yl}-methanone

https://huagongshe.com/reaction/18110

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Diethylether waterHCID 21584184—
反応物Potassium trifluoroacetateHCID 23662811—
反応物1-{(S)-2-[(5-Bromo-pyrimidin-2-ylamino)methyl]-pyrrolidin-1-yl}-1-[5-(4-fluoro-phenyl)-2-methyl-thiazol-4-yl]-methanoneHCID 67089741—
触媒Copper iodideHCID 83717—
溶媒DimethylformamideHCID 6228—
生成物1-[5-(4-Fluoro phenyl)-2-methyl-thiazol-4-yl]-1-{(S)-2-[(5-trifluoromethyl-pyrimidin-2-ylamino)-methyl]-pyrrolidin-1-yl}-methanoneHCID 670903200.3%

反応手順

To the compound from Example 194 (0.36 g) in dimethylformamide (5 ml) was added potassium trifluoroacetate (0.23 g), copper iodide (0.3 g) and toluene (5 ml) and the resulting mixture heated at reflux under Dean-Stark conditions for 3 h, before refluxing for a further 20 h. The reaction mixture was cooled, poured into water/ether and filtered through kieselguhr. The aqueous layer from the filtrate was extracted with ether, and the combined ether extracts washed with water, dried and evaporated. The aqueous was re-extracted with dichloromethane and the extract evaporated. The combined extracts were chromatographed on silica gel, eluting with methanol-dichloromethane mixtures, to afford the title product (0.001 g). Mass Spectrum (Electrospray LC/MS): Found 466 (MH+). C21H19F4N5OS requires 465.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741329B2
出典データセットuspto-grants-2010_06
ORD IDord-4ef542aa7a634e42a6b1cfff2811ea52
出典メモuspto-grants-2010_06