反应 #67009

ord-7edf2078af034c5e8e68ff894daec008

反应方程式

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

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度gradually warmed to room temperature
  2. 2
    workup.STIRRINGAfter stirring overnight
  3. 3
    其他the solvent and excess hydrogen chloride were removed

实验过程

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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08524743B2uspto-grants-2013_09