Triethylamine → HCID 10856105, compound

HRID 977638Notes

Reaction equation

HRID 977638 reaction equation
[C:1](Cl)(=[O:4])[CH2:2][CH3:3].[SH:6][C:7]1[C:12]([CH3:13])=[CH:11][CH:10]=[CH:9][N:8]=1.C(N(CC)CC)C>C(Cl)Cl>[C:1]([S:6][C:7]1[C:12]([CH3:13])=[CH:11][CH:10]=[CH:9][N:8]=1)(=[O:4])[CH2:2][CH3:3]

Participants

5

Procedure

1.21 ml (13.9 mmole) of propionyl chloride were added dropwise, whilst ice-cooling and under an atmosphere of nitrogen, to a solution of 1.46 g (11.7 mmole) of 2-mercapto-3-methylpyridine (prepared as described in Preparation7) and 1.94 ml (13.9 mmole) of triethylamine in 15 ml of methylene chloride, and the resulting mixture was stirred for 1 hour. At the end of this time, the reaction mixture was mixed with 50 ml of methylene chloride, and the mixture was washed with a saturated aqueous solution of sodium hydrogencarbonate. It was then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The residue was purified by medium pressure column chromatography through silica gel, using a 5:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 1.89 g (yield 89%) of the title compound as a light yellow oil.

Workup

  1. washthe mixture was washed with a saturated aqueous solution of sodium hydrogencarbonate
  2. dry with materialIt was then dried over anhydrous magnesium sulfate
  3. customthe solvent was removed by distillation under reduced pressure
  4. customThe residue was purified by medium pressure column chromatography through silica gel
  5. additionby volume mixture of hexane and ethyl acetate as the eluent

Sources & evidence

ORD record
ord-0b28d16c24fb40168b5fc3382e30ce37
Source dataset
uspto-grants-1997_03
Patent number
US05614624

Reaction notes

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