Methyl iodide → 2'-O-methyl-5-methyl-2thiouridine

HRID 962887

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HRID 962887 반응식
[CH3:1][C:2]1[C:3](=[O:18])[NH:4][C:5](=[S:17])[N:6]([CH:16]=1)[C@@H:7]1[O:15][C@H:12]([CH2:13][OH:14])[C@@H:10]([OH:11])[C@H:8]1[OH:9].[CH2:19]([Sn](=O)CCCC)CCC.CI>CN(C=O)C.[I-].C([N+](CCCC)(CCCC)CCCC)CCC.C(Cl)Cl>[CH3:19][O:9][C@@H:8]1[C@H:10]([OH:11])[C@@H:12]([CH2:13][OH:14])[O:15][C@H:7]1[N:6]1[CH:16]=[C:2]([CH3:1])[C:3](=[O:18])[NH:4][C:5]1=[S:17]

참가 물질

7

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온도
50 °C

실험 절차

To a stirred solution of 5-methyl-2-thiouridine (0.500 g, 1.8 mmol) in DMF (10 ml) is added dibutyltin oxide (0.500 g, 2.0 mmol), tetrabutyl ammonium iodide (0.738 g, 2 mmol), and methyl iodide (1.022 g, 7.2 mmol). The reaction flask is sealed and heated at 50° C. for 16 hours. The mixture is cooled and another portion of methyl iodide is added (1.022 g, 7.2 mmol) and the reaction heated for an additional 16 hours. At the end of this time, the reaction mixture is cooled to room temperature and diluted with methylene chloride and chromatographed using a methylene chloride/methanol gradient. The appropriate fractions are collected and concentrated to give 2'-O-methyl-5-methyl-2-thiouridine.

후처리

  1. customThe reaction flask is sealed
  2. temperatureThe mixture is cooled
  3. temperaturethe reaction heated for an additional 16 hours
  4. temperatureAt the end of this time, the reaction mixture is cooled to room temperature
  5. customchromatographed
  6. customThe appropriate fractions are collected
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2da0b64c028e433bb4021f234546db8f
출처 데이터셋
uspto-grants-1998_06
특허 번호
US05760202

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