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HRID 38791作成日:2026年10月26日

tert-Butanol → Tert-butyl{2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}carbamate

https://huagongshe.com/reaction/38791

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物TriethylamineHCID 8471—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物Sodium BicarbonateHCID 516892—
反応物2-(3-Chlorophenylamino)-4-trifluoromethylpyrimidine-5-carboxylic acidHCID 16719655—
生成物Tert-butyl{2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}carbamateHCID 68404320—

反応条件

温度90 °C

反応手順

To a mixture of 2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidine-5-carboxylic acid (307 mg), triethylamine (162 μL), and tert-butyl alcohol (9 mL) was added diphenylphosphorylazide (250 μL), followed by stirring at 90° C. for 7 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution (50 mL), followed by extraction with ethyl acetate (50 mL), and then the extract was washed with saturated brine (30 mL). The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain tert-butyl {2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}carbamate (270 mg) as a pale yellow powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524727B2
出典データセットuspto-grants-2013_09
ORD IDord-cc9395f6678a4328bd0405ccf8eb2dbe
出典メモuspto-grants-2013_09