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Hydrazine → HCID 178446229, 화합물

HRID 600574
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HRID 600574 반응식
[CH2:1]([N:8]1[C:16]2[C:15](SC)=[N:14][C:13](=[O:19])[N:12]([CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[C:11]=2[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:25][NH2:26]>>[CH2:1]([N:8]1[C:16]2/[C:15](=[N:25]/[NH2:26])/[NH:14][C:13](=[O:19])[N:12]([CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[C:11]=2[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 9321HydrazineHCID 598538237-Benzyl-6-(methylthio)-3-pentyl-3,7-dihydro-2H-purin-2-one

생성물 1

HCID 178446229HCID 178446229, 화합물수율 60%

반응 조건

온도
100 °C

실험 절차

7-Benzyl-6-(methylthio)-3-pentyl-3,7-dihydro-2H-purin-2-one (1.2 g, 3.5 mmol) and hydrazine (10 mL, 100 mmol) were mixed. After being stirred at 100° C. overnight, the solution was concentrated in vacuum. The residue was dissolved in DMSO and purified using preparative LCMS. The product fractions were collected and lyophilized to provide the product as a white powder (0.56 g, 60% yield). LCMS calculated for C17H23N6O (M+H): 327.2. found: 327.1.

후처리

  1. concentrationthe solution was concentrated in vacuum
  • dissolutionThe residue was dissolved in DMSO
  • custompurified
  • customThe product fractions were collected
  • 출처 및 근거

    ORD 기록
    ord-80362fcfd1114cac9cd9ec3a5cef8120
    출처 데이터셋
    uspto-grants-2011_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07902205B2

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