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4-Nitrophenethyl bromide → 1,4-Bis[2-(4-nitrophenyl)ethyl]piperazine

HRID 1519554
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HRID 1519554 반응식
Cl.[N+:2]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][CH2:12][N:13]2[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]2)=[CH:7][CH:6]=1)([O-:4])=[O:3].Br[CH2:20][CH2:21][C:22]1[CH:27]=[CH:26][C:25]([N+:28]([O-:30])=[O:29])=[CH:24][CH:23]=1>CN(C=O)C>[N+:2]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][CH2:12][N:13]2[CH2:14][CH2:15][N:16]([CH2:20][CH2:21][C:22]3[CH:23]=[CH:24][C:25]([N+:28]([O-:30])=[O:29])=[CH:26][CH:27]=3)[CH2:17][CH2:18]2)=[CH:7][CH:6]=1)([O-:4])=[O:3]
참가 물질반응 조건실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 792664-Nitrophenethyl bromideHCID 666440061-[2-(4-Nitrophenyl)ethyl]piperazine hydrochloride

생성물 1

HCID 523378371,4-Bis[2-(4-nitrophenyl)ethyl]piperazine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

To a solution of 1-[2-(4-nitrophenyl)ethyl]piperazine hydrochloride (30 mg, 0.11 mmol) in DMF (2 mL) was added 1-(2-bromoethyl)-4-nitrobenzene (31 mg, 1.3 mmol) and TEA (46 uL, 0.33 mmol). The mixture was heated to 80° C. for 16 hours. LC showed some desired product at that point. The desired 1,4-bis[2-(4-nitrophenyl)ethyl]piperazine was purified by mass-directed HPLC. LC-MS (IE, m/z): 385 [M+1]+. (0.052 μM)

출처 및 근거

ORD 기록
ord-8a79e3ec105c4f4388ce75a52946219b
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073882B2

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