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HRID 1667675作成日:2026年10月25日

Hexafluorophosphate → 2-Azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide

https://huagongshe.com/reaction/1667675

反応式

関与物質

役割名称HCID仕込み量
反応物HexafluorophosphateHCID 9886—
反応物Ammonium ChlorideHCID 25517—
反応物DiisopropylethylamineHCID 81531—
反応物2-Azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acidHCID 86642802—
反応物HCID 178484285HCID 178484285—
溶媒DimethylformamideHCID 6228—
生成物2-Azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amideHCID 8664280383.8%

反応手順

A solution of 2.20 g (7.01 mmole) of 2-azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid, 38 mL of dimethylformamide, 3.47 g (8.85 mmole) of 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium, 3-oxide, hexafluorophosphate(1-) (1:1) and 3.75 mL (21.53 mmole) of ethyldiisopropylamine was stirred at room temperature for 23 minutes, then 0.5733 g (10.72 mmole) of ammonium chloride was added. The mixture was stirred for 2.25 hours, then concentrated under reduced pressure and partitioned between 300 mL of ethyl acetate and 75 mL of water. The ethyl acetate layer was washed twice with 60 mL of water, twice with 55 mL of saturated aqueous sodium bicarbonate, once with 50 mL of brine, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with ethyl acetate-hexanes (gradient 10:90-100-:0) to give 1.841 g 2-azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide as a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08044213B2
出典データセットuspto-grants-2011_10
ORD IDord-1b75d78143bf4d98a6034b2c037b5ab2
出典メモuspto-grants-2011_10