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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 492295생성일: 2026년 10월 25일

Potassium Iodide → N-[[[(2,6-diisopropylphenyl)amino]carbonyl]methyl]-N-pentyl-N-[[2'-[N-(triphenylmethyl)tetrazol-5-yl]-1,1'-biphenyl-4-yl]methyl]amine

https://huagongshe.com/reaction/492295

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물TriethylamineHCID 8471—
반응물2-Chloro-N-(2,6-diisopropylphenyl)acetamideHCID 2363774—
반응물pentyl[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-ylmethyl]amineHCID 19024425—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-[[[(2,6-diisopropylphenyl)amino]carbonyl]methyl]-N-pentyl-N-[[2'-[N-(triphenylmethyl)tetrazol-5-yl]-1,1'-biphenyl-4-yl]methyl]amineHCID 6885318533%

반응 조건

온도80 °C

반응 단계

N-(Chloroacetyl)-2,6-diisopropylaniline (196.3 mg), N-pentyl-N-[[2′-[N-(triphenylmethyl)tetrazol-5-yl]-1,1′-biphenyl-4-yl]methyl]amine (430.0 mg), potassium iodide (70 mg) and triethylamine (0.6 g) were suspended in dimethylformamide (3 mL). The resulting mixture was heated to about 80° C., and then stirred at that temperature. Three hours later, the reaction mixture was cooled, ethyl acetate (30 mL) was added, and the mixture was washed four times with brine (50 mL, each). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was subjected to chromatography on a silica gel column (hexane/ethyl acetate) to afford N-[[[(2,6-diisopropylphenyl)amino]carbonyl]methyl]-N-pentyl-N-[[2′-[N-(triphenylmethyl)tetrazol-5-yl]-1,1′-biphenyl-4-yl]methyl]amine (196.4 mg). Yield: 33%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07531576B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-8c9e5fa1e80247efa0c1083a5993c353
출처 메모uspto-grants-2009_05