4-Methoxybenzenethiol → HCID 22181674, compound

HRID 1796326Notes

Reaction equation

HRID 1796326 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([SH:9])=[CH:5][CH:4]=1.[H-].[Na+].I[C:13]1[C:14](=[O:20])[NH:15][C:16]([CH3:19])=[CH:17][CH:18]=1>CN(C=O)C.[Cu]I>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9][C:13]2[C:14](=[O:20])[NH:15][C:16]([CH3:19])=[CH:17][CH:18]=2)=[CH:5][CH:4]=1

Participants

6

Conditions

Temperature
25 °C

Procedure

4-Methoxythiophenol (1.7 mL, 13.85 mmol) was added to a suspension of NaH 60% in oil (831 mg, 20.80 mmol) in DMF (30 mL) at 0° C., and the mixture was allowed to warm to 25° C. 3-Iodo-6-methyl-1H-pyridin-2-one (3 g, 12.78 mmol) was added to the solution at 0° C., followed by CuI (533 mg, 2.8 mmol). The reaction was stirred at 25° C. for 1 h and heated at 120° C. for 5 h. Then it was allowed to cool and partitioned between CH2Cl2 (30 mL) and 9:1 NH4Cl/NH4OH (30 mL) and stirred for 15 min. The mixture was extracted with CH2Cl2 (3×70 mL each) and the combined CH2Cl2 extracts were washed with water (3×30 mL), brine, dried and stripped in vacuo to give the crude product (3.6 g), which was further purified by washing with ether to give 2.93 g of 3-(4-methoxyphenylsulfanyl)-6-methyl-1H-pyridin-2-one which was used in the next step.

Workup

  1. temperatureheated at 120° C. for 5 h
  2. temperatureto cool
  3. custompartitioned between CH2Cl2 (30 mL) and 9:1 NH4Cl/NH4OH (30 mL)
  4. stirringstirred for 15 min
  5. extractionThe mixture was extracted with CH2Cl2 (3×70 mL each)
  6. washthe combined CH2Cl2 extracts were washed with water (3×30 mL), brine
  7. customdried
  8. customto give the crude product (3.6 g), which
  9. customwas further purified
  10. washby washing with ether

Sources & evidence

ORD record
ord-7f1f781a7a35421480370fd945f11a86
Source dataset
uspto-grants-2006_04
Patent number
US07030145B2

Reaction notes

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