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1-Methylpiperazine → HCID 59349549, 화합물

HRID 415121
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인쇄 미리보기

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HRID 415121 반응식
Br[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:12]=[CH:11][C:9]([NH2:10])=[C:8]([N+:13]([O-:15])=[O:14])[CH:7]=1.[CH3:16][N:17]1[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1>O>[CH3:16][N:17]1[CH2:22][CH2:21][N:20]([CH2:2][CH2:3][CH2:4][O:5][C:6]2[CH:12]=[CH:11][C:9]([NH2:10])=[C:8]([N+:13]([O-:15])=[O:14])[CH:7]=2)[CH2:19][CH2:18]1
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참가 물질

4

반응물 2

HCID 531671-MethylpiperazineHCID 220406544-(3-Bromopropoxy)-2-nitroaniline

생성물 1

HCID 59349549HCID 59349549, 화합물수율 60%

시약·촉매·용매 1

HCID 962Water용매

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온도
100 °C

실험 절차

A 100 mL flask was charged with 4-(3-bromopropoxy)-2-nitroaniline (2.2 g, 8.02 mmol) and 4-methylpiperazine (10 mL) and stirred at 100° C. The reaction was monitored by LCMS and complete in 30 minutes. The reaction mixture was treated with water (100 mL) and sonicated in an ultrasonic bath. The resulting solid were filtered off and dried under reduced pressure to give 1.5 g of 4-(3-(4-methylpiperazin-1-yl)propoxy)-2-nitroaniline (60% yield). MS (EI): 295 (MH+).

후처리

  1. customsonicated in an ultrasonic bath
  2. filtrationThe resulting solid were filtered off
  3. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-6de5295784f54487b7b9fa7bfdc7b83f
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08088767B2

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