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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1667667생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1667667

반응식

참여 물질

역할이름HCID투입량
반응물HexafluorophosphateHCID 9886—
반응물Ammonium ChlorideHCID 25517—
반응물DiisopropylethylamineHCID 81531—
반응물2-Azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acidHCID 86642799—
반응물HCID 178484285HCID 178484285—
용매DimethylformamideHCID 6228—
생성물2-Azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amideHCID 8664280078.9%

반응 단계

To a solution of 1.76 g (5.60 mmole) of 2-azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid and 30 mL of dimethylformamide was added 2.75 g (7.01 mmole) of 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium, 3-oxide, hexafluorophosphate(1-) (1:1) and 3.0 mL (17.2 mmole) of ethyldiisopropylamine. The mixture was stirred for 18 minutes, then 0.4541 g (8.49 mmole) of ammonium chloride was added. The mixture was concentrated under reduced pressure and diluted with 350 mL of ethyl acetate and 75 mL of water. The ethyl acetate layer was washed with 50 mL of water, 50 mL of saturated aqueous sodium bicarbonate, 50 mL of brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with ethyl acetate-hexanes (gradient 10:90-100:0) to give 1.384 g of 2-azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044213B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-56a479eb834a49269374a54bd7b5d9ad
출처 메모uspto-grants-2011_10