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HRID 499184作成日:2026年10月27日

Pyridine → 2,2,2-Trichloroethyl (3-tert-butyl-1-methyl-1H-pyrazol-5-yl)carbamate

https://huagongshe.com/reaction/499184

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Ethyl AcetateHCID 8857—
反応物2,2,2-Trichloroethyl chloroformateHCID 87063—
反応物3-tert-Butyl-1-methyl-1H-pyrazol-5-amineHCID 2735287—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2,2,2-Trichloroethyl (3-tert-butyl-1-methyl-1H-pyrazol-5-yl)carbamateHCID 59420872—

反応条件

温度0 °C

反応手順

To an ice-cooled solution of 5-tert-butyl-2-methyl-2H-pyrazol-3-ylamine (0.50 g, 3.26 mmol) and pyridine (0.27 mL, 3.29 mmol) in THF (THF, 10 mL) is added 2,2,2-trichloroethyl chloroformate (0.44 mL, 3.29 mmol). The reaction mixture is stirred at 0° C. for 30 min and then warmed to room temperature for 2 hours. Then the reaction mixture is distributed between ethyl acetate (100 mL) and water (100 mL). The aqueous phase is extracted with ethyl acetate (50 mL). The combined organic phases are washed with saturated NaCl (2×50 mL) and dried over anhydrous magnesium sulfate. After removal of solvent, the residue is purified on a silica gel chromatography by washing with ethyl acetate to provide a white solid (0.83 g, 78%, ES+(m/z) 329.9 [M+H]).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07767674B2
出典データセットuspto-grants-2010_08
ORD IDord-8ad732784b564b859fc67bd23cbc8055
出典メモuspto-grants-2010_08