Reaction #323303

ord-233cc87da07d4246a5e14925e78a594b

Reaction equation

[NH2-].[Na+]
sodium amide
CN1CCC(O)C1
1-methyl-3-pyrrolidinol
C[O-].[Na+]
sodium methoxide
NC(=O)c1ccccc1O
salicylamide
Cc1ccccc1S(=O)(=O)Cl
o-toluenesulfonylchloride
CN1CCC(Oc2ccccc2C(N)=O)C1
2-(1-Methyl-3-pyrrolidinyloxy)benzamide

Conditions

Temperature
70°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Othera temperature of 50° C
  2. 2
    TemperatureThe mixture was cooled
  3. 3
    Temperaturewhile maintaining a temperature of 20°-30° C. with an ice bath
  4. 4
    Washwashed with water
  5. 5
    DryingThe toluene solution was dried with sodium sulfate
  6. 6
    Concentrationconcentrated
  7. 7
    workup.DISSOLUTIONThe residue, dissolved in 500 ml of dimethylformamide
  8. 8
    workup.ADDITIONwas added to a reaction mixture
  9. 9
    Otherprepared
  10. 10
    Otherthe mixture was worked up as in preparation 1

Procedure

To 85.6 g (2.2 moles) of sodium amide in 1.5 liter of dry toluene was added 202 g (2 moles) of 1-methyl-3-pyrrolidinol so as not to exceed a temperature of 50° C. The mixture was then heated to 70° C. for 4.5 hours. The mixture was cooled and 381 g (2 moles) of o-toluenesulfonylchloride was added at a rapid drop while maintaining a temperature of 20°-30° C. with an ice bath. The mixture was stirred at room temperature for 2.5 hours and washed with water. The toluene solution was dried with sodium sulfate and concentrated. The residue, dissolved in 500 ml of dimethylformamide, was added to a reaction mixture prepared by adding 119 g (2.2 moles) of sodium methoxide and 274 g (2.0 moles) of salicylamide to one liter of dimethylformamide and the mixture was worked up as in preparation 1. Yield of product was 170 g (38%), m.p. 116°-118° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04642343uspto-grants-1987_02