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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

반응식

참여 물질

역할이름HCID투입량
반응물HexafluorophosphateHCID 9886—
반응물Ammonium ChlorideHCID 25517—
반응물DiisopropylethylamineHCID 81531—
반응물2-[6-(4-Methyl-piperazin-1-ylmethyl)-benzoimidazol-1-yl]-4-phenyl-thiazole-5-carboxylic acidHCID 67446253—
반응물HCID 178484285HCID 178484285—
용매DimethylformamideHCID 6228—
생성물2-[6-(4-Methyl-piperazin-1-ylmethyl)-benzoimidazol-1-yl]-4-phenyl-thiazole-5-carboxylic acid amideHCID 4683461964.7%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044213B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-e2d3d1a3b4ab41ff84f8e8fc75c9c515
출처 메모uspto-grants-2011_10