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Ammonia → 2'-Deoxy-2'-fluoro-2'-methyluridine

HRID 1027361
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HRID 1027361 반응식
C([C@@:9]1([OH:34])[C@@H:13]([CH:14](C(=O)C2C=CC=CC=2)[OH:15])[O:12][C@@H:11]([N:24]2[CH:31]=[CH:30][C:28](=[O:29])[NH:27][C:25]2=[O:26])[C@@:10]1([F:33])[CH3:32])(=O)C1C=CC=CC=1.N>CO>[F:33][C@:10]1([CH3:32])[C@H:9]([OH:34])[C@@H:13]([CH2:14][OH:15])[O:12][C@H:11]1[N:24]1[CH:31]=[CH:30][C:28](=[O:29])[NH:27][C:25]1=[O:26]
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 86638038HCID 86638038, 화합물

생성물 1

HCID 113115032'-Deoxy-2'-fluoro-2'-methyluridine수율 60%

시약·촉매·용매 1

HCID 887Methanol용매2회

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온도
0 °C

실험 절차

To a solution of 3′,5′-dibenzoyl-2′-Deoxy-2′-fluoro-2′-C-methyluridine (1.5 g, 1 eq) in MeOH (10 mL) was added a solution of saturated ammonia in MeOH (20 mL). The reaction mixture was stirred at 0° C. for 30 min, and then warmed to room temperature slowly. After the reaction mixture was stirred for another 18 hours, the reaction mixture was evaporated under reduced pressure to give the residue, which was purified by column chromatography to afford pure compound 2′-deoxy-2′-fluoro-2′-C-methyluridine (500 mg, Yield: 60%).

후처리

  1. temperaturewarmed to room temperature slowly
  2. stirringAfter the reaction mixture was stirred for another 18 hours
  3. customthe reaction mixture was evaporated under reduced pressure
  4. customto give the residue, which
  5. customwas purified by column chromatography

출처 및 근거

ORD 기록
ord-2580934a949246a5afa781505c56596e
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08735372B2

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