Reaction #68824

ord-9a6d4185f94349fdb3f966984385e18c

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherevaporated to dryness
  2. 2
    OtherThe product thus obtained

Procedure

0.786 g of tert-butyl ester of 4-(1,1-dioxo-1lambda6-thiomorpholin-4-yl)-piperidine-1-carboxylic acid is put in 5 ml of dichloromethane. 12.3 ml of 4M hydrochloric acid in dioxane is added at room temperature. The solution is stirred for 18 h and evaporated to dryness. The product thus obtained is returned to the basic state by means of tetraalkylammonium carbonate resin at a rate of 2 g per mmol. 0.555 g of 4-piperidin-4-yl-thiomorpholine 1,1-dioxide is obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530473B2uspto-grants-2013_09