3-bromo-2-chloro-5-(4-ethylpiperazin-1-ylsulfonyl)pyridine → HCID 22052242, compound

HRID 2305411Notes

Reaction equation

HRID 2305411 reaction equation
[Br:1][C:2]1[C:3](Cl)=[N:4][CH:5]=[C:6]([S:8]([N:11]2[CH2:16][CH2:15][N:14]([CH2:17][CH3:18])[CH2:13][CH2:12]2)(=[O:10])=[O:9])[CH:7]=1.[O-:20][CH2:21][CH3:22].[Na+]>C(O)C>[Br:1][C:2]1[C:3]([O:20][CH2:21][CH3:22])=[N:4][CH:5]=[C:6]([S:8]([N:11]2[CH2:16][CH2:15][N:14]([CH2:17][CH3:18])[CH2:13][CH2:12]2)(=[O:10])=[O:9])[CH:7]=1

Participants

4

Reactant 2

HCID 10342243-bromo-2-chloro-5-(4-ethylpiperazin-1-ylsulfonyl)pyridineHCID 2723922Sodium ethoxide

Product 1

HCID 22052242HCID 22052242, compoundYield 95%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 3-bromo-2-chloro-5-(4-ethylpiperazin-1-ylsulfonyl)pyridine (Preparation 9; 6.60 g, 17.9 mmol) and sodium ethoxide (6.09 g, 89.55 mmol) in ethanol (100 mL) was heated under reflux for 18 hours, then cooled. The reaction mixture was concentrated under reduced pressure, the residue partitioned between water (100 mL) and ethyl acetate (100 mL), and the layers separated. The aqueous phase was extracted with ethyl acetate (2×100 mL), the combined organic solutions dried (MgSO4) and evaporated under reduced pressure to afford the title compound as a brown solid (6.41 g, 95%).

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 18 hours
  3. temperaturecooled
  4. concentrationThe reaction mixture was concentrated under reduced pressure
  5. customthe residue partitioned between water (100 mL) and ethyl acetate (100 mL)
  6. customthe layers separated
  7. extractionThe aqueous phase was extracted with ethyl acetate (2×100 mL)
  8. dry with materialthe combined organic solutions dried (MgSO4)
  9. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-8c963473a5274bc3ba83dea197e1b3a1
Source dataset
uspto-grants-2002_08
Patent number
US06440982B1

Reaction notes

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