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Acetoxyacetyl chloride → (7-Mercapto[1,3]thiazolo[5,4-d]pyrimidin-2-yl)methanol

HRID 32588
ノート
印刷プレビュー

反応式

HRID 32588 の反応式
[NH2:1][C:2]1[C:3]([SH:9])=[N:4][CH:5]=[N:6][C:7]=1[SH:8].[C:10](OCC(Cl)=O)(=[O:12])[CH3:11]>N1C=CC=CC=1>[SH:8][C:7]1[C:2]2[N:1]=[C:11]([CH2:10][OH:12])[S:9][C:3]=2[N:4]=[CH:5][N:6]=1
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

4

反応物 2

HCID 26297Acetoxyacetyl chlorideHCID 1785081365-Aminopyrimidine-4,6-dithiol2 回

生成物 1

HCID 178519945(7-Mercapto[1,3]thiazolo[5,4-d]pyrimidin-2-yl)methanol

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
115 °C

実験手順

A cooled (ice bath) suspension of 5-aminopyrimidine-4,6-dithiol (Intermediate 41) (40.0 g) in pyridine (500 mL) was stirred under an inert atmosphere atmosphere. Acetoxyacetyl chloride (38 mL) was added over 10 minutes, the ice bath was removed and the mixture stirred at ambient temperature overnight. The mixture was concentrated in vacuo and azeotroped three times with toluene (200 mL). The residue was suspended in 2N HCl, and heated at 115° C. for 5 hours, and allowed to cool to ambient temperature overnight. The resulting suspension was filtered, washed with water (200 mL) and ether (200 mL) to give the title compound as a pale brown solid (48.3 g, 97%) (containing 10% of (7-mercapto[1,3]thiazolo[5,4-d]pyrimidin-2-yl)methyl acetate);

後処理

  1. temperatureA cooled
  2. customthe ice bath was removed
  3. stirringthe mixture stirred at ambient temperature overnight
  4. concentrationThe mixture was concentrated in vacuo
  5. customazeotroped three times with toluene (200 mL)
  6. temperatureto cool to ambient temperature overnight
  7. filtrationThe resulting suspension was filtered
  8. washwashed with water (200 mL) and ether (200 mL)

出典と根拠

ORDレコード
ord-7d12168941a74394a75a0b8745e7b7a3
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07427616B2

反応ノート

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