반응 #2464333

ord-f84111d866654a2fb57d332e3a84508c

반응 방정식

ClCCCOCCc1ccc2sccc2c1
5-[2-(3-chloropropoxy)ethyl]-1-benzothiophene
CC(=O)NC1CNC1
N-(3-azetidinyl)acetamide
O
water
CCOC(C)=O
ethyl acetate
CC(=O)NC1CN(CCCOCCc2ccc3sccc3c2)C1
N-(1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinyl)acetamide
수율 37.4%

반응 조건

온도
90°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added to the solution
  2. 2
    온도After the reaction mixture was cooled
  3. 3
    기타the organic layer was separated
  4. 4
    세척The organic layer was washed with water
  5. 5
    건조a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONdistilled under reduced pressure
  7. 7
    기타to remove the solvent
  8. 8
    기타The residue was purified by a column chromatography (eluent; chloroform:methanol=7:1)

실험 절차

In 8 mL of N,N-dimethylformamide was dissolved 0.80 g of 5-[2-(3-chloropropoxy)ethyl]-1-benzothiophene, and 1.20 g of N-(3-azetidinyl)acetamide was added to the solution, after which the resulting mixture was stirred at 90° C. for 12 hours. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform:methanol=7:1) to obtain 0.39 g of N-(1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinyl)acetamide as a light-yellow oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07468443B2uspto-grants-2008_12