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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Formic Acid → 2-Thioxanthine, TX3

HRID 883556
ノート
印刷プレビュー

反応式

HRID 883556 の反応式
[NH2:1][C:2]1[C:3](=[O:16])[NH:4][C:5](=[S:15])[N:6]([CH2:9][CH:10]2[CH2:14][CH2:13][CH2:12][O:11]2)[C:7]=1[NH2:8].[CH:17](O)=O>>[O:11]1[CH2:12][CH2:13][CH2:14][CH:10]1[CH2:9][N:6]1[C:7]2[N:8]=[CH:17][NH:1][C:2]=2[C:3](=[O:16])[NH:4][C:5]1=[S:15]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 284Formic AcidHCID 86601059HCID 86601059、化合物

生成物 1

HCID 103548422-Thioxanthine, TX3収率 87%

反応条件

温度
70 °C

実験手順

5,6-Diamino-1-(2-tetrahydro furyl-methyl)-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one (0.25 g, 1.0 mmol) was dissolved in formic acid (1 mL) and heated at 70° C. for 0.5 h. After a few minutes a pink solid formed in the solution. The excess of formic acid was evaporated off and the resulting solid dissolved in 10% sodium hydroxide solution (4 mL). This solution was heated at 70° C. for 40 minutes, then neutralized with 2M hydrochloric acid. The resulting precipitate was collected by filtration, washed with water and dried, giving pure product (0.23 g, 87%).

後処理

  1. customAfter a few minutes a pink solid formed in the solution
  • customThe excess of formic acid was evaporated off
  • dissolutionthe resulting solid dissolved in 10% sodium hydroxide solution (4 mL)
  • temperatureThis solution was heated at 70° C. for 40 minutes
  • filtrationThe resulting precipitate was collected by filtration
  • washwashed with water
  • customdried
  • 出典と根拠

    ORDレコード
    ord-98e9ed8ec108468a9e08b5f5fb723b07
    出典データセット
    uspto-grants-2012_08
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08236951B2

    反応ノート

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    このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート