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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexafluorophosphate | HCID 9886 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-Azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid | HCID 86642799 | — |
| 반응물 | HCID 178484285 | HCID 178484285 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-Azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide | HCID 86642800 | 78.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08044213B2 |
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| 출처 데이터셋 | uspto-grants-2011_10 |
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| ORD ID | ord-56a479eb834a49269374a54bd7b5d9ad |
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| 출처 메모 | uspto-grants-2011_10 |
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