Réaction #1857576

ord-f61cfcb52d464991a88d958cf15bf19e

Équation de réaction

CC(C)(C)OC(=O)N1CCC(c2nc(C=O)cs2)CC1
tert-butyl 4-(4-formyl-1,3-thiazol-2-yl)piperidine-1-carboxylate
Cl
hydrogen chloride
O=Cc1csc(C2CC[NH2+]CC2)n1.[Cl-]
4-(4-Formyl-1,3-thiazol-2-yl)piperidinium chloride

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températuregradually warmed to room temperature
  2. 2
    workup.STIRRINGAfter stirring overnight
  3. 3
    Autrethe solvent and excess hydrogen chloride were removed

Mode opératoire

To tert-butyl 4-(4-formyl-1,3-thiazol-2-yl)piperidine-1-carboxylate (10 g) was added dropwise, at 0° C., a 4 molar solution of hydrogen chloride in 1,4-dioxane (100 ml). The reaction mixture was stirred at 0° C. and then gradually warmed to room temperature. After stirring overnight, the solvent and excess hydrogen chloride were removed. This gave 4-(4-formyl-1,3-thiazol-2-yl)piperidinium chloride (9 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09247748B2uspto-grants-2016_02