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1-(4-Pyridyl)piperazine → HCID 18918505, 화합물

HRID 1291835
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HRID 1291835 반응식
[CH2:1]([N:3]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10](Cl)[CH:11]=2)[C:6](=[O:14])[C:5]([C:15]([OH:17])=[O:16])=[CH:4]1)[CH3:2].[N:18]1[CH:23]=[CH:22][C:21]([N:24]2[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]2)=[CH:20][CH:19]=1>CO>[CH2:1]([N:3]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([N:27]3[CH2:28][CH2:29][N:24]([C:21]4[CH:22]=[CH:23][N:18]=[CH:19][CH:20]=4)[CH2:25][CH2:26]3)[CH:11]=2)[C:6](=[O:14])[C:5]([C:15]([OH:17])=[O:16])=[CH:4]1)[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 705171-(4-Pyridyl)piperazineHCID 156185627-Chloro-1-ethyl-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

생성물 1

HCID 18918505HCID 18918505, 화합물수율 24.8%

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
200 °C

실험 절차

A mixture of 1-ethyl-7-chloro-4-quinolon-3-ylcarboxylic acid (182 mg) and 1-(4-pyridyl) piperazine (125 mg ) was heated to 200° C. for 20 minutes. The mixture was cooled and methanol (5 ml) was added. The resulting solid was filtered and washed with methanol (10 ml) to give the title compound (68 mg), as a solid: NMR (d6DMSO) δ 1.4(t,3H), 3.75°-3.85(m,4H), 3.9-4.0(m,4H), 4.55(q,2H), 6.9(d,1H), 7.2(d,2H), 7.3(dd,1H), 8.2(d,1H), 8.3(d,2H), 8.9(s,1H); m/e 379(M+H)+

후처리

  1. temperatureThe mixture was cooled
  2. filtrationThe resulting solid was filtered
  3. washwashed with methanol (10 ml)

출처 및 근거

ORD 기록
ord-4673dcbf5b5144309f0ca32a2da1a7d0
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05753659

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