Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1667683생성일: 2026년 10월 26일
Hexafluorophosphate → 2-[6-(4-Methyl-piperazin-1-ylmethyl)-benzoimidazol-1-yl]-4-phenyl-thiazole-5-carboxylic acid amide
https://huagongshe.com/reaction/1667683
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexafluorophosphate | HCID 9886 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-[6-(4-Methyl-piperazin-1-ylmethyl)-benzoimidazol-1-yl]-4-phenyl-thiazole-5-carboxylic acid | HCID 67446253 | — |
| 반응물 | HCID 178484285 | HCID 178484285 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-[6-(4-Methyl-piperazin-1-ylmethyl)-benzoimidazol-1-yl]-4-phenyl-thiazole-5-carboxylic acid amide | HCID 46834619 | 64.7% |
반응 단계
To a mixture of 0.022 g (0.05 mmole) of 2-[6-(4-methyl-piperazin-1-ylmethyl)-benzoimidazol-1-yl]-4-phenyl-thiazole-5-carboxylic acid (I.1b), 0.023 g (0.06 mmole) of 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium, 3-oxide, hexafluorophosphate(1-) (1:1), 0.004 g of ammonium chloride and 1 mL of dimethylformamide was added 0.026 mL (0.15 mmole) of ethyldiisopropylamine. The mixture was stirred at ambient temperature for 1 hour. Solids were removed by filtration and the filtrate purified by reverse phase silica gel chromatography, eluting with acetonitrile-water (gradient 10:90-90:10) to give 0.014 g of 2-[6-(4-methyl-piperazin-1-ylmethyl)-benzoimidazol-1-yl]-4-phenyl-thiazole-5-carboxylic acid amide (I.1) as a white powder. MH+/Z=433.
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-e2d3d1a3b4ab41ff84f8e8fc75c9c515 |
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| 출처 메모 | uspto-grants-2011_10 |
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