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HCID 14410678、化合物 → 2'-methyl-2'-deoxyidenecytidine

HRID 1647268
ノート
印刷プレビュー

反応式

HRID 1647268 の反応式
[CH2:1]=[C:2]1[C@H:6]([OH:7])[C@@H:5]([CH2:8][OH:9])[O:4][C@H:3]1[N:10]1[CH:25]=[CH:24][C:14]([NH:15]C(=O)C2C=CC=CC=2)=[N:13][C:11]1=[O:12]>N>[CH2:1]=[C:2]1[C@H:6]([OH:7])[C@@H:5]([CH2:8][OH:9])[O:4][C@H:3]1[N:10]1[CH:25]=[CH:24][C:14]([NH2:15])=[N:13][C:11]1=[O:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 14410678HCID 14410678、化合物

生成物 1

HCID 30059132'-methyl-2'-deoxyidenecytidine収率 96.1%

試薬・触媒・溶媒 1

HCID 222Ammonia溶媒

実験手順

A solution of 139 mg (0.5 mmol) of 2'-deoxy-2'-methylidene-4-N-benzoylcytidine in 10 ml of methanolic ammonia was stirred at room temperature for 6 hours to cause reaction and the solvent distilled off under reduced pressure. The residue was developed through a silica gel column (1.6×10 cm, 20% ethanol-chloroform being used as a solvent for elution), fractions containing the desired compound collected, 2 ml of 1N hydrochloric acid added, and the solvent distilled off under reduced pressure. The residue was crystallized from acetone-methanol to obtain 115 mg (yield 83%) of 2'-deoxy-2'-methylidenecytidine.

後処理

  1. customreaction
  • distillationthe solvent distilled off under reduced pressure
  • washused as a solvent for elution), fractions
  • additioncontaining the desired compound
  • customcollected
  • addition2 ml of 1N hydrochloric acid added
  • distillationthe solvent distilled off under reduced pressure
  • customThe residue was crystallized from acetone-methanol
  • 出典と根拠

    ORDレコード
    ord-0edd365ebadc4e6dbc89147617872d06
    出典データセット
    uspto-grants-1995_07
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US05430139

    反応ノート

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