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Dimethyl Sulfate → HCID 86069929, 화합물

HRID 2109967
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HRID 2109967 반응식
[CH3:1][N:2]([CH3:16])[CH2:3][CH2:4][N:5]([CH3:15])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N+:12]([O-:14])=[O:13].[S:17]([O:22]C)([O:20][CH3:21])(=[O:19])=[O:18]>C(#N)C>[CH3:21][O:20][S:17]([O-:22])(=[O:19])=[O:18].[CH3:1][N+:2]([CH3:21])([CH3:16])[CH2:3][CH2:4][N:5]([CH3:15])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N+:12]([O-:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6497Dimethyl SulfateHCID 23562754HCID 23562754, 화합물

생성물 1

HCID 86069929HCID 86069929, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

5.0 g (22.4 mmol) of the free amine from Step 10.2 was dissolved in 50 ml of acetonitrile and to this solution was added dropwise with agitation over a period of 10 min 2.83 g (22.4 mmol) of dimethyl sulfate. The reaction temperature gradually rose to 45° C. and a precipitate formed. After an agitation period of 3 hours, the mixture was filtered and the filter cake was washed with a small amount of acetonitrile and then dried at 40° C. under vacuum.

후처리

  • customgradually rose to 45° C.
  • customa precipitate formed
  • filtrationAfter an agitation period of 3 hours, the mixture was filtered
  • washthe filter cake was washed with a small amount of acetonitrile
  • customdried at 40° C. under vacuum
  • 출처 및 근거

    ORD 기록
    ord-3c05f019956241e7a038d326300a85e3
    출처 데이터셋
    uspto-grants-2009_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07517367B2

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