3-(Chloromethyl)pyridine → 3-(3-Pyridylmethyl)2-nitromethylenethiazolidine

HRID 359505Notes

Reaction equation

HRID 359505 reaction equation
[N+:1]([CH:4]=[C:5]1[NH:9][CH2:8][CH2:7][S:6]1)([O-:3])=[O:2].[H-].[Na+].[H][H].[N:14]1[CH:19]=[CH:18][CH:17]=[C:16]([CH2:20]Cl)[CH:15]=1>C(#N)C>[N:14]1[CH:19]=[CH:18][CH:17]=[C:16]([CH2:20][N:9]2[CH2:8][CH2:7][S:6][C:5]2=[CH:4][N+:1]([O-:3])=[O:2])[CH:15]=1

Participants

6

Reactant 4

HCID 183583-(Chloromethyl)pyridineHCID 24758Sodium hydrideHCID 38355832-Nitromethylene-thiazolidineHCID 178418361HCID 178418361, compound

Product 1

HCID 542512073-(3-Pyridylmethyl)2-nitromethylenethiazolidineYield 10.6%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent2×

Procedure

2-Nitromethylenethiazolidine (2.9 g) was suspended in dry acetonitrile (30 ml), and 60% sodium hydride (0.9 g) was added under a nitrogen stream. Then, the mixture was stirred at room temperature until the generation of hydrogen ceased. A solution of 3-picolyl chloride (3.2 g) in dry acetonitrile (5 ml) was added, and the mixture was stirred at room temperature for 3 hours. Acetonitrile was distilled off under reduced pressure. Dichloromethane was added to the residue., and the mixture was washed with water. Dichloromethane was then distilled off from the dichloromethane layer. The remaining oily product was purified by column chromatography to give the desired 3-(3-pyridylmethyl)2-nitromethylenethiazolidine (0.5 g).

Workup

  1. distillationAcetonitrile was distilled off under reduced pressure
  2. additionDichloromethane was added to the residue
  3. wash, and the mixture was washed with water
  4. distillationDichloromethane was then distilled off from the dichloromethane layer
  5. customThe remaining oily product was purified by column chromatography

Sources & evidence

ORD record
ord-7902fd8e653f4c2680288271ec9c3142
Source dataset
uspto-grants-1991_03
Patent number
US05001138

Reaction notes

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