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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

반응식

참여 물질

역할이름HCID투입량
반응물1,1-DibromoethaneHCID 11201—
반응물Potassium CarbonateHCID 11430—
반응물Potassium bisulfateHCID 516920—
반응물2-[5-Benzyloxycarbonylamino-2-(2-nitro-benzenesulfonylamino)-pentanoylamino]-3-naphthalen-2-yl-propionic acid methyl esterHCID 20806410—
용매DimethylformamideHCID 6228—
생성물2-[3-(3-Benzyloxycarbonylamino-propyl)-4-(2-nitro-benzene-sulfonyl)-2-oxo-piperazin-1-yl]-3-naphthalen-2-yl-propionic acid methyl esterHCID 20806407—

반응 조건

온도55 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087759B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-be983771db2641cba6b6dd0a8290a239
출처 메모uspto-grants-2006_08