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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 366151생성일: 2026년 10월 23일

Fmoc-Gly-OH → ({2-[2-(N-(tert-butoxycarbonyl)-N-methylamino)ethyl]phenylcarbamoyl}methyl)carbamic acid ((9-fluorenyl)methyl) ester

https://huagongshe.com/ko/reaction/366151

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참여 물질

역할이름HCID투입량
반응물Fmoc-Gly-OHHCID 93124—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물N-(2-(2-aminophenyl)ethyl)-N-methylcarbamic acid tert-butyl esterHCID 10800697—
용매DichloromethaneHCID 6344—
생성물({2-[2-(N-(tert-butoxycarbonyl)-N-methylamino)ethyl]phenylcarbamoyl}methyl)carbamic acid ((9-fluorenyl)methyl) esterHCID 2067751695.6%

반응 조건

온도0 °C

반응 단계

2-(((9-Fluorenyl)methoxycarbonyl)amino)acetic acid (2.49 g, 2.79 mmol) was suspended in dichloromethane (40 ml). The suspension was cooled to 0° C. N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (802 mg, 4.19 mmol) was added. The reaction mixture was stirred for 30 min at 0° C. A solution of N-(2-(2-aminophenyl)ethyl)-N-methylcarbamic acid tert-butyl ester (698 mg, 2.79 mmol) in dichloromethane (15 ml) was added. The reaction mixture was stirred for 16 h, while it was warming up to room temperature. It was diluted with dichloromethane (100 ml) and washed with brine (100 ml). The aqueous solution was extracted with dichloromethane (2×30 ml). The combined organic layers were dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (80 g), using ethyl acetate/heptane (1:1) as eluent, to give 1.412 g of ({2-[2-(N-(tert-butoxycarbonyl)-N-methylamino)ethyl]phenylcarbamoyl}methyl)carbamic acid ((9-fluorenyl)methyl) ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06127354
출처 데이터셋uspto-grants-2000_10
ORD IDord-12be51cfe44d4db1b5c0573c91873f78
출처 메모uspto-grants-2000_10