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Phosphorus tribromide → 2-Propylthiazol-5-amine

HRID 607139
ノート
印刷プレビュー

反応式

HRID 607139 の反応式
[C:1]([NH:6][CH2:7][C:8]([NH2:10])=O)(=[S:5])[CH2:2][CH2:3][CH3:4].P(Br)(Br)Br>C(OCC)(=O)C>[CH2:2]([C:1]1[S:5][C:8]([NH2:10])=[CH:7][N:6]=1)[CH2:3][CH3:4]
参加物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 24614Phosphorus tribromide2 回HCID 866146222-Thiobutyrylamino-acetamide

生成物 1

HCID 451217592-Propylthiazol-5-amine

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒2 回

実験手順

A solution of the product of Example 5C (395 mg, 2.465 mmol) in anhydrous ethyl acetate (12 mL) was treated with phosphorous tribromide (0.189 mL, 1.972 mmol) under a nitrogen atmosphere and stirred at room temperature for 20 minutes. Added additional phosphorous tribromide (0.050 mL) and let stir for 5 minutes. The reaction mixture was diluted with ethyl acetate (50 mL) and washed with saturated aqueous sodium bicarbonate (25 mL). The aqueous wash was extracted with ethyl acetate (2×50 mL), and the organic extracts were combined and washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum giving the title compound. Purification by silica gel flash chromatography with 3% methanol/methylene afforded the title product (175 mg, 1.23 mmol, 50%).

後処理

  1. stirringlet stir for 5 minutes
  2. washwashed with saturated aqueous sodium bicarbonate (25 mL)
  3. washThe aqueous wash
  4. extractionwas extracted with ethyl acetate (2×50 mL)
  5. washwashed with brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-5702a827e8f24c159de73b4f955a732a
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07915411B2

反応ノート

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