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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1667675생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1667675

반응식

참여 물질

역할이름HCID투입량
반응물HexafluorophosphateHCID 9886—
반응물Ammonium ChlorideHCID 25517—
반응물DiisopropylethylamineHCID 81531—
반응물2-Azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acidHCID 86642802—
반응물HCID 178484285HCID 178484285—
용매DimethylformamideHCID 6228—
생성물2-Azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amideHCID 8664280383.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044213B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-1b75d78143bf4d98a6034b2c037b5ab2
출처 메모uspto-grants-2011_10