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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1584758생성일: 2026년 10월 27일

Water → 1,1-Dimethylethyl 2-(4-(4-fluorophenyl)-1-piperazinyl)-2-oxo-1-(phenylmethyl)ethylcarbamate

https://huagongshe.com/reaction/1584758

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물Boc-Phe-ONpHCID 111308—
반응물1-(4-Fluorophenyl)piperazine dihydrochlorideHCID 16211916—
용매DimethylformamideHCID 6228—
생성물1,1-Dimethylethyl 2-(4-(4-fluorophenyl)-1-piperazinyl)-2-oxo-1-(phenylmethyl)ethylcarbamateHCID 5380473592.2%

반응 단계

To a solution of 1-(4-fluorophenyl)piperazine dihydrochloride (2.53 g, 10 mmol) in N,N-dimethylformamide (40 ml) were added triethylamine (2.8 ml, 20 mmol) and N-tert-butoxycarbonylphenylalanine p-nitrophenyl ester (2.65 g, 10 mmol) in the order mentioned and the mixture was stirred at room temperature overnight. This reaction mixture was poured into cold water and extracted with ethyl acetate. The extract was washed with 1% aqueous ammonia, saturated saline, 0.1N-hydrochloric acid, saturated saline, saturated aqueous sodium hydrogen carbonate solution, and saturated saline in the order mentioned and the organic layer was dried over anhydrous magnesium sulfate and further concentrated under reduced pressure. The residue was purified by silica gel column chromatography using chloroform-methanol (50:1) to provide 1,1-dimethylethyl 2-(4-(4-fluorophenyl)-1-piperazinyl)-2-oxo-1-(phenylmethyl)ethylcarbamate (2.7 g, 92.2%) as colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05935959
출처 데이터셋uspto-grants-1999_08
ORD IDord-7399c94bf60d46a6832e0fbc9c260721
출처 메모uspto-grants-1999_08