Reaction #684992

ord-d1781644ee04440a86ad24410d7cbabd

Reaction equation

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
Yield 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
Yield 88.4%

Solvents

Conditions

Temperature
60°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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.v1Patent: US07897594B2uspto-grants-2011_03