반응 #649567

ord-d06c4b5c118a48db8753c609d92c963b

반응 방정식

CC(=O)NC1CNC1
N-(3-azetidinyl)acetamide
ClCCCOCCc1ccc2sccc2c1
5-(2-(3-chloropropoxy)ethyl)-1-benzothiophene
O
water
CCOC(C)=O
ethyl acetate
CC(=O)NC1CN(CCCOCCc2ccc3sccc3c2)C1
light yellow oil
수율 37.4%
CC(=O)NC1CN(CCCOCCc2ccc3sccc3c2)C1
N-(1-(3-(2-(1-benzothiophene-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
    온도After cooling
  2. 2
    기타an organic layer was separated
  3. 3
    세척The organic layer was successively washed with water
  4. 4
    건조a saturated saline solution, and then dried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONThereafter, the solvent was distilled away under a reduced pressure
  6. 6
    기타The residue was purified by column chromatography (eluent; chloroform:methanol=7:1)

실험 절차

0.80 g of 5-(2-(3-chloropropoxy)ethyl)-1-benzothiophene was dissolved in 8 ml of N,N-dimethylformamide. Thereafter, 1.20 g of N-(3-azetidinyl)acetamide was added to the obtained solution, and the obtained mixture was stirred at 90° C. for 12 hours. After cooling, water and ethyl acetate were added to the reaction mixture, and an organic layer was separated. The organic layer was successively washed with water and a saturated saline solution, and then dried over anhydrous magnesium sulfate. Thereafter, the solvent was distilled away under a reduced pressure. The residue was purified by column chromatography (eluent; chloroform:methanol=7:1), so as to obtain 0.39 g of a light yellow oil product, N-(1-(3-(2-(1-benzothiophene-5-yl)ethoxy)propyl)-3-azetidinyl)acetamide.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08067406B2uspto-grants-2011_11