发明授权
US5202243A Method of hydroxylating 3-[2-(benzoxazol-2-yl)ethyl]-5-ethyl-6-methyl-2-(1H)-pyridinone by incubation with liver slices 失效
通过与肝切片一起温育3- [2-(苯并恶唑-2-基)乙基] -5-乙基-6-甲基-2-(1H) - 吡啶酮的羟基化方法

  • 专利标题: Method of hydroxylating 3-[2-(benzoxazol-2-yl)ethyl]-5-ethyl-6-methyl-2-(1H)-pyridinone by incubation with liver slices
  • 专利标题(中): 通过与肝切片一起温育3- [2-(苯并恶唑-2-基)乙基] -5-乙基-6-甲基-2-(1H) - 吡啶酮的羟基化方法
  • 申请号: US852483
    申请日: 1992-03-16
  • 公开(公告)号: US5202243A
    公开(公告)日: 1993-04-13
  • 发明人: Suresh K. Balani
  • 申请人: Suresh K. Balani
  • 申请人地址: NJ Rahway
  • 专利权人: Merck & Co., Inc.
  • 当前专利权人: Merck & Co., Inc.
  • 当前专利权人地址: NJ Rahway
  • 主分类号: C12P17/16
  • IPC分类号: C12P17/16
Method of hydroxylating
3-[2-(benzoxazol-2-yl)ethyl]-5-ethyl-6-methyl-2-(1H)-pyridinone by
incubation with liver slices
摘要:
Incubation of 3-[2-benzoxazol-2-yl)ethyl]-5-ethyl-6-methyl-2-(1H)-pyridinone ##STR1## with a preparation from mammalian organ yields as biotransformation product the 6-hydroxymethyl analog. This product is useful in the prevention or treatment of infection by HIV and the treatment of AIDS.
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