Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39270생성일: 2026년 10월 23일
Nalpha-(9-fluorenylmethoxycarbonyl)-Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine → Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine
https://huagongshe.com/ko/reaction/39270
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Nalpha-(9-fluorenylmethoxycarbonyl)-Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine | HCID 86762028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | piperidine N,N-dimethylformamide | HCID 23501187 | — |
| 생성물 | Nepsilon-(4,4-bis(diallylphosphoryl)butyryl)-L-lysine | HCID 86762027 | 85.6% |
반응 단계
A solution of 90 (502 mg, 0.616 mmol) in piperidine/DMF (0.05:1, 5 mL) was stirred at room temperature for 18 hr. After diluting with ethyl acetate (40 mL) the organic layer was washed with water and brine then dried over Na2SO4 and concentrated in vacuo. The crude material was purified by silica gel chromatography (methanol in ethyl acetate, 5% over 5 column volumes then 5 to 30% over 10 column volumes) using a Biotage Horizon™ apparatus resulting in the colourless liquid 91 (249 mg, 68%): 1H NMR (400 MHz, CDCl3) δ 1.39-1.74 (m, 6H), 1.45 (s, 9H), 2.21-2.35 (m, 2H), 2.51 (t, J=7.4, 2H), 2.55 (tt, J=6.9, 23.9, 1H), 3.19-3.25 (m, 2H), 3.29 (dd, J=5.2, 7.6, 1H), 4.58-4.63 (m, 8H), 5.25 (dq, J=1.3, 10.3, 4H), 5.38 (dq, J=1.4, 17.1, 4H), 5.90-6.00 (m, 4H), 6.14 (bd, J=4.9, 1H): 31P (162 MHz, CDCl3) δ 24.67 (s, 2P).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524691B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-9ace8feb681144c797b9b24e1829a87f |
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| 출처 메모 | uspto-grants-2013_09 |
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