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Water → Pyrimidine-2,4,5-triol

HRID 36846
ノート
印刷プレビュー

反応式

HRID 36846 の反応式
BrBr.[NH:3]1[CH:8]=[CH:7][C:6](=[O:9])[NH:5][C:4]1=[O:10].N1C=CC=NC=1.[OH2:17]>>[OH:17][C:7]1[C:6](=[O:9])[NH:5][C:4](=[O:10])[NH:3][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 962WaterHCID 1174Uracil2 回HCID 9260PyrimidineHCID 24408Bromine

生成物 1

HCID 73268Pyrimidine-2,4,5-triol

実験手順

According to the synthetic method shown in Scheme A, above, bromine is added dropwise to an ice-cooled solution or suspension of a pyrimidine-2,4(1H,3H)-dione derivative of formula (III) in water until the solution or suspension is colored pale yellow. The pyrimidine-2,4(1H,3H)-dione derivatives of formula (III) are prepared, for example, by the methods described in Heterocyclic Compounds 16, The pyrimidine supplement II, D. J. Brown, An Interscience Publication, John Willy & Sons, New York, 1985, Table LVIII, page 728. To the resulting pale yellow solution or suspension is added carefully an ice cold saturated aqueous NaHCO3 solution. The resulting reaction mixture is refluxed, the solvent is removed and the residue is recrystallized from an appropriate solvent or chromatographed over silica-gel to give a 5-hydroxyprimidine-2,4(1H,3H)-dione derivative of formula (IV).

後処理

  1. temperaturecooled
  2. customThe resulting reaction mixture
  3. temperatureis refluxed
  4. customthe solvent is removed
  5. customthe residue is recrystallized from an appropriate solvent
  6. customchromatographed over silica-gel

出典と根拠

ORDレコード
ord-dfa4a8f2f7244247bf8a9676065aef98
出典データセット
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05418231

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート