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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Fmoc-Gly-OH | HCID 93124 | — |
| 반응물 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 반응물 | N-(2-(2-aminophenyl)ethyl)-N-methylcarbamic acid tert-butyl ester | HCID 10800697 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | ({2-[2-(N-(tert-butoxycarbonyl)-N-methylamino)ethyl]phenylcarbamoyl}methyl)carbamic acid ((9-fluorenyl)methyl) ester | HCID 20677516 | 95.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06127354 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-12be51cfe44d4db1b5c0573c91873f78 |
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| 출처 메모 | uspto-grants-2000_10 |
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