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1-Benzyl-1,2-dihydropyridine-4-carboxamide → HCID 15680051, 화합물

HRID 2051316
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HRID 2051316 반응식
[I-].[F:2][CH2:3][CH2:4][N:5]([N:21]=[O:22])[C:6]([NH:8][CH2:9][CH2:10][O:11][C:12](C1[CH2+]=CC=CN1C)=[O:13])=[O:7].[CH2:23]([N:30]1[CH:38]=[CH:37][C:33](C(N)=O)=[CH:32][CH2:31]1)C1C=CC=CC=1>CO>[F:2][CH2:3][CH2:4][N:5]([N:21]=[O:22])[C:6]([NH:8][CH2:9][CH2:10][O:11][C:12]([C:37]1[CH2:33][CH:32]=[CH:31][N:30]([CH3:23])[CH:38]=1)=[O:13])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 132279601-Benzyl-1,2-dihydropyridine-4-carboxamide

생성물 1

HCID 15680051HCID 15680051, 화합물수율 55%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of the quaternary nitrosourea prepared in Example 126 (0.426 g, 1 mmol) and 1-benzyl-1,2-dihydroisonicotinamide (0.21 g, 1 mmol) in 25 mL of anhydrous methanol was stirred at 0° C. for 4 hours under nitrogen. The solvent was evaporated in vacuo at about 30° C. and the residue was suspended in chloroform, filtered and flash chromatographed on a short column of neutral alumina. The title compound was obtained in 55% yield after elution with chloroform and was assigned the structure ##STR154## consistent with UV analysis.

후처리

  1. customThe solvent was evaporated in vacuo at about 30° C.
filtration
filtered
  • customflash chromatographed on a short column of neutral alumina
  • 출처 및 근거

    ORD 기록
    ord-3f3104466a3d4945a7de9a58b90c47a6
    출처 데이터셋
    uspto-grants-1991_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05017566

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