Réaction #684992

ord-d1781644ee04440a86ad24410d7cbabd

Équation de réaction

OC1CN(CCCOCCc2ccc3sccc3c2)C1
1-(3-(2-(1-benzothiophene-5-yl)ethoxy)propyl)-3-azetidinol
O=C(O)/C=C\C(=O)O
maleic acid
O=C(O)/C=C\C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
achromatic crystal
Rendement 88.4%
O=C(O)/C=C\C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
1-(3-(2-(1-benzothiophene-5-yl)ethoxy)propyl)-3-azetidinol maleate
Rendement 88.4%

Solvants

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction mixture was gradually cooled
  2. 2
    AutreThereafter, precipitated crystals
  3. 3
    Filtrationwere collected by filtration

Mode opératoire

8.00 g of 1-(3-(2-(1-benzothiophene-5-yl)ethoxy)propyl)-3-azetidinol was dissolved in 56 ml of acetone. Thereafter, 3.19 g of maleic acid was added thereto, and the obtained mixture was heated to 60° C. for dissolution. The reaction mixture was gradually cooled, and it was then stirred at 5° C. for 30 minutes. Thereafter, precipitated crystals were collected by filtration, so as to obtain 9.89 g of an achromatic crystal, 1-(3-(2-(1-benzothiophene-5-yl)ethoxy)propyl)-3-azetidinol maleate.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07897594B2uspto-grants-2011_03