Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8528생성일: 2026년 10월 24일
1,1-Dibromoethane → 2-[3-(3-Benzyloxycarbonylamino-propyl)-4-(2-nitro-benzene-sulfonyl)-2-oxo-piperazin-1-yl]-3-naphthalen-2-yl-propionic acid methyl ester
https://huagongshe.com/ko/reaction/8528
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,1-Dibromoethane | HCID 11201 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Potassium bisulfate | HCID 516920 | — |
| 반응물 | 2-[5-Benzyloxycarbonylamino-2-(2-nitro-benzenesulfonylamino)-pentanoylamino]-3-naphthalen-2-yl-propionic acid methyl ester | HCID 20806410 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-[3-(3-Benzyloxycarbonylamino-propyl)-4-(2-nitro-benzene-sulfonyl)-2-oxo-piperazin-1-yl]-3-naphthalen-2-yl-propionic acid methyl ester | HCID 20806407 | — |
반응 단계
A mixture of 2-[5-benzyloxycarbonylamino-2-(2-nitro-benzenesulfonylamino)-pentanoylamino]-3-naphthalen-2-yl-propionic acid methyl ester, 40, (2.4 g, 3.63 mmol), dibromoethane (3.8 mL, 4.36 mmol), potassium carbonate (5.0 g, 36.3 mmol) in DMF (50 mL) is stirred at 55° C. for 18 hours. The reaction mixture is cooled to room temperature, treated with 1M KHSO4 and the resulting solution is extracted with ethyl acetate. The crude product is purified over silica (sequential elution with EtOAc/hexanes mixtures 1:2, 1:1, 100% EtOAc, then EtOAc with 5% MeOH) to afford 2.76 g of the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07087759B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-be983771db2641cba6b6dd0a8290a239 |
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| 출처 메모 | uspto-grants-2006_08 |
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