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HRID 444793作成日:2026年10月26日

Potassium Carbonate → Tert-butyl 3-(4,6-bistrifluoromethylpyridin-2-yl)propylcarbamate

https://huagongshe.com/reaction/444793

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物9-Borabicyclo(3.3.1)nonaneHCID 78966—
反応物tert-butyl N-(prop-2-en-1-yl)carbamateHCID 4067274—
反応物Pyridine, 2-bromo-4,6-bis(trifluoromethyl)-HCID 85875928—
触媒palladium(II) acetateHCID 167845—
触媒Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 3-(4,6-bistrifluoromethylpyridin-2-yl)propylcarbamateHCID 8665069474%

反応手順

To a stirred solution of tert-butyl allylcarbamate (1.95 g, 12.4 mmol) in THF (12 mL), 0.5 mol/L 9-borabicyclo[3.3.1]nonane (29.8 mL, 14.9 mmol) was added under argon atmosphere at room temperature. After stirred at room temperature for 4 h, a solution of 2-bromo-4,6-bistrifluoromethylpyridine (3.65 g, 12.4 mmol) in DMF (12 mL), Pd(OAc)2 (278 mg, 1.24 mmol), DPPF (859 mg, 1.55 mmol) and K2CO3 (2.92 g, 21.1 mmol) were added to the reaction mixture and stirred at room temperature for 7 h. To the reaction mixture, water was added and the crude product was extracted with EtOAc, washed with brine, dried over NaSO4 and the solvent was removed in vacuo. The crude product was purified by column chromatography (Hexane:EtOAc 10:1→2:1) to yield tert-butyl 3-(4,6-bistrifluoromethylpyridin-2-yl)propylcarbamate (3.41 g, 74%) as a colorless solid. 1H NMR (CDCl3, 400 MHz) δ 1.44 (9H, s), 1.96-2.03 (2H, m), 2.98-3.02 (2H, m), 3.20-3.25 (2H, m), 4.71 (1H, brs), 7.59 (1H, s), 7.72 (1H, s). CIMS (+) 373 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08476261B2
出典データセットuspto-grants-2013_07
ORD IDord-a2417668deaa487fb23f75a774839b97
出典メモuspto-grants-2013_07