Thiourea → HCID 22648874、化合物

HRID 393283ノート

反応式

HRID 393283 の反応式
[NH2:1][C:2]([NH2:4])=[S:3].Br[CH2:6][C:7]([C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[C:11]([CH3:16])[CH:10]=1)=O>O1CCOCC1>[NH2:1][C:2]1[S:3][CH:6]=[C:7]([C:9]2[CH:14]=[CH:13][C:12]([OH:15])=[C:11]([CH3:16])[CH:10]=2)[N:4]=1

参加物

4

反応条件

温度
25 °C

実験手順

Thiourea (79.8 mg, 1.05 mmol) was added to a solution of 2-bromo-1-(4-hydroxy-3-methylphenyl)ethanone (200 mg, 0.87 mmol) in 1,4-dioxane (15 mL). The reaction mixture was stirred at 25° C. for 24 h. The resulting suspension was filtered and the solid was washed with 1,4-dioxane and dried under reduced pressure. The solid was suspended in water (30 mL), pH 7 buffer solution (15 mL) was added and the mixture was extracted with EtOAc (3×50 mL). The combined organic layers were successively washed with water (20 mL) and brine (20 mL), dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (Hexane:EtOAc, 1:1) to give the title compound (180 mg, 100% yield).

後処理

  1. filtrationThe resulting suspension was filtered
  2. washthe solid was washed with 1,4-dioxane
  3. customdried under reduced pressure
  4. additionpH 7 buffer solution (15 mL) was added
  5. extractionthe mixture was extracted with EtOAc (3×50 mL)
  6. washThe combined organic layers were successively washed with water (20 mL) and brine (20 mL)
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by flash chromatography (Hexane:EtOAc, 1:1)

出典と根拠

ORDレコード
ord-96fcdb23cd8d45479baa46c5247ac730
出典データセット
uspto-grants-2004_10
特許番号
US06806265B2

反応ノート

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