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Methyl iodide → HCID 21430644, 화합물

HRID 1730365
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반응식

HRID 1730365 반응식
[C:1]([NH:9][CH:10]1[CH2:15][CH2:14][N:13]([CH2:16][CH2:17][CH2:18][C:19]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[O:20])[CH2:12][CH2:11]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[I:27][CH3:28]>CN(C)C=O>[I-:27].[C:1]([NH:9][CH:10]1[CH2:15][CH2:14][N+:13]([CH3:28])([CH2:16][CH2:17][CH2:18][C:19]([C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)=[O:20])[CH2:12][CH2:11]1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 100892541-(3-Benzoylpropyl)-4-benzamidopiperidine

생성물 1

HCID 21430644HCID 21430644, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of 4-benzamido-1-(4-phenyl-4-oxobutyl)-piperidine (1.75 g., 0.005 mole) and iodomethane (7.10 g., 0.05 mole) in N,N-dimethylformamide (5 ml.) was stirred for 150 hours at room temperature. The reaction mixture was filtered and the residue was washed with fresh N,N-dimethylformamide and then diethyl ether.

후처리

  1. filtrationThe reaction mixture was filtered
  • washthe residue was washed with fresh N,N-dimethylformamide
  • 출처 및 근거

    ORD 기록
    ord-963688f9ce3041d89b0a8c293bdd7271
    출처 데이터셋
    uspto-grants-1976_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US03992389

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