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1-Methyl-1,2-dihydropyridine → HCID 86745532, 화합물

HRID 2371523
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HRID 2371523 반응식
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17]Br)=[CH:9][CH:8]=1.[CH3:19][N:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH2:21]1>C(O)C>[Br-:1].[Br-:1].[CH3:19][N+:20]1([CH:16]([CH3:17])[CH2:15][CH2:14][CH2:13][C:10]2[CH:9]=[CH:8][CH:7]=[CH:12][CH:11]=2)[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]1.[CH3:19][N+:20]1([CH:3]([CH3:2])[CH2:4][CH2:5][CH2:6][C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 125655021-Methyl-1,2-dihydropyridineHCID 19907362HCID 19907362, 화합물

생성물 1

HCID 86745532HCID 86745532, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 376 mg of 1,4-bis(5-bromopentyl)benzene in 2 ml of absolute ethanol, 365 μl of N-methylpyridine was added, and the mixture was refluxed for 5 hours. After concentration under a reduced pressure and addition of acetone, and the mixture was allowed to stand overnight. The product was filtered and recrystallized from ethanol (0.5 ml)--acetone (2 ml) to obtain 455 mg of the title compound as a colorless crystal.

후처리

  • temperaturethe mixture was refluxed for 5 hours
  • concentrationAfter concentration
  • additionunder a reduced pressure and addition of acetone
  • filtrationThe product was filtered
  • customrecrystallized from ethanol (0.5 ml)
  • 출처 및 근거

    ORD 기록
    ord-9ce773c66a6f42c5b3f942e546aec926
    출처 데이터셋
    uspto-grants-1992_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05093370

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