Réaction #2254218

ord-b14ece93e0a243089b140a347f7152d3

Équation de réaction

C=CCC1(NN)CCOC2(CCCC2)C1
[9-(prop-2-en-1-yl)-6-oxaspiro[4.5]decan-9-yl]hydrazine
CCN(CC)CC
Et3N
CN(C)C=CC=O
3-dimethylaminoacrolein
C=CCC1(n2cccn2)CCOC2(CCCC2)C1
1-[9-(prop-2-en-1-yl)-6-oxaspiro[4.5]decan-9-yl]-1H-pyrazole
Rendement 31.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe solution was refluxed for 3 h
  2. 2
    AutreThe solvent removed
  3. 3
    Autrethe residue was purified on 25 g Biotage snap column
  4. 4
    Lavageeluted with 0-18% EtOAc in Hex (12CV)

Mode opératoire

A solution of [9-(prop-2-en-1-yl)-6-oxaspiro[4.5]decan-9-yl]hydrazine (250 mg, 1.0 mmol) in 4 mL of i-PrOH were added Et3N and 3-dimethylaminoacrolein. The solution was refluxed for 3 h and then at 50° C. for 2 d. The solvent removed and the residue was purified on 25 g Biotage snap column, eluted with 0-18% EtOAc in Hex (12CV) to give 1-[9-(prop-2-en-1-yl)-6-oxaspiro[4.5]decan-9-yl]-1H-pyrazole (80 mg, 31% yield).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09044469B2uspto-grants-2015_06