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Volumn 21, Issue 1, 2010, Pages 67-69

A convenient synthesis of ezetimibe analogs as cholesterol absorption inhibitors

Author keywords

Cholesterol absorption inhibitor; Ezetimibe; Synthesis

Indexed keywords


EID: 70749135704     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2009.08.009     Document Type: Article
Times cited : (2)

References (7)
  • 5
    • 70749144162 scopus 로고    scopus 로고
    • Synthesis of compound 6: To a solution of 5 (5.08 g, 13.55 mmol) and Ph3P (3.54 g, 13.55 mmol) in THF (40 mL) at 0 °C was added dropwise, DEAD (2.47 mL, 13.55 mmol, The solution was stirred for 8 h and then evaporated. The residue was purified on Si-gel to provide 1.58 g (32.7, of compound 6 as a white solid. Spectral data of compound 6: 1H NMR (CDCl3, 300 MHz, δ 7.26-6.88 (m, 8H, Ph, 4.64-4.63 (d, 1H, J, 2.1, CH2-CH-CH, 3.80 (s, 3H, Ph-OCH3, 3.66 (s, 3H, COOCH3, 3.14-3.08 (m, 1H, CH2-CH-CH, 2.61-2.48 (m, 2H, CH2-CH2-COO, 2.26-2.18 (m, 2H, CH2-CH2-COO, 13C NMR (CDCl3, 300 MHz, δ 167.8, 163.7, 160.5, 157.3, 133.8, 129.2, 127.5, 127.4, 127.4, 127.3, 127.2, 127.1, 118.4, 118.3, 115.9, 115.6, 115.4, 115.1, 114.6, 73.1, 61.0, 60.3, 55.3, 36.6, 24.9; IR KBr, cm-1, υ: 2986, 2917, 1740, 1610, 150
    • + 380.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.