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((2S,3S,5R)-5-(2-amino-6-chloro-9H-purin-9-yl)-3-azidotetrahydrofuran-2-yl)methanol → 3'-Azido-2,6-diaminopurine-2',3'-dideoxyriboside

HRID 2408268
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인쇄 미리보기

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HRID 2408268 반응식
[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[C@@H:11]2[O:15][C@H:14]([CH2:16][OH:17])[C@@H:13]([N:18]=[N+:19]=[N-:20])[CH2:12]2)=[C:4](Cl)[N:3]=1.[NH3:22].CO>>[N:18]([C@H:13]1[CH2:12][C@H:11]([N:8]2[CH:7]=[N:6][C:5]3[C:9]2=[N:10][C:2]([NH2:1])=[N:3][C:4]=3[NH2:22])[O:15][C@@H:14]1[CH2:16][OH:17])=[N+:19]=[N-:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 476464((2S,3S,5R)-5-(2-amino-6-chloro-9H-purin-9-yl)-3-azidotetrahydrofuran-2-yl)methanolHCID 21705897Ammonia methanol

생성물 1

HCID 721823'-Azido-2,6-diaminopurine-2',3'-dideoxyriboside수율 58%

반응 조건

온도
80 °C

실험 절차

A mixture of compound 77 (190 mg, 0.61 mmol) and NH3/CH3OH (30 mL) was heated to 80° C. at seal bomb for 18 h, then cooled to room temperature. The reaction mixture was evaporated and purified by flash column chromatography with dichloromethane:ethyl acetate:methanol=7:7:1 to obtain the white solid 100 mg 58%.

후처리

  • customat seal bomb for 18 h
  • temperaturecooled to room temperature
  • customThe reaction mixture was evaporated
  • custompurified by flash column chromatography with dichloromethane
  • 출처 및 근거

    ORD 기록
    ord-36a32f448df84fb3bf88f6eef23ab399
    출처 데이터셋
    uspto-grants-2014_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08815829B2

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