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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexafluorophosphate | HCID 9886 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-Azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid | HCID 86642802 | — |
| 반응물 | HCID 178484285 | HCID 178484285 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-Azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide | HCID 86642803 | 83.8% |
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
| 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-1b75d78143bf4d98a6034b2c037b5ab2 |
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| 출처 메모 | uspto-grants-2011_10 |
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