Norprostol → Methyl 3-hydroxy-2-(3-hydroxy-3-methyl-1-octynyl)-5-oxocyclopentaneheptanoate
反応式
OC1CC(=O)C(CCCCCCC(OC)=O)=C1.CC(OC1CCCCO1)(CCCCC)C#C[Al](C#CC(OC1CCCCO1)(C)CCCCC)C#CC(OC1CCCCO1)(C)CCCCC.[Ga].[B].[OH:69][CH:70]1[CH2:74][C:73](=[O:75])[CH:72]([CH2:76][CH2:77][CH2:78][CH2:79][CH2:80][CH2:81][C:82]([O:84][CH3:85])=[O:83])[CH:71]1[C:86]#[C:87][C:88]([CH3:101])([O:94]C1CCCCO1)[CH2:89][CH2:90][CH2:91][CH2:92][CH3:93]>C(O)(=O)C>[OH:69][CH:70]1[CH2:74][C:73](=[O:75])[CH:72]([CH2:76][CH2:77][CH2:78][CH2:79][CH2:80][CH2:81][C:82]([O:84][CH3:85])=[O:83])[CH:71]1[C:86]#[C:87][C:88]([OH:94])([CH3:101])[CH2:89][CH2:90][CH2:91][CH2:92][CH3:93]参加物
7
反応物 5
生成物 1
試薬・触媒・溶媒 1
実験手順
The 3-hydroxy-3-alkylated acetylenic compounds of this invention are prepared by employing the appropriately alkylated alkynyl boron, alkynyl gallium or alkynyl aluminum reactant. For example, treatment of methyl 3-hydroxy-5-oxocyclopent-1-eneheptanoate with tri(3methyl-3-[tetrahydropyran-2-yl]oxy-1-octynyl) aluminum, gallium or boron affords the epimeric methyl 3-hydroxy-2-(3-methyl-3-[tetrahydropyran-2-yl]oxy-1-octynyl)-5-oxocyclopentaneheptanoate. Typically, that compound may be hydrolyzed with a hydrolyzing agent such as hydrolytic acid, e.g. aqueous acetic acid, to yield the instant methyl 3-hydroxy-2-(3-hydroxy-3-methyl-1-octynyl)-5-oxocyclopentaneheptanoate.
出典と根拠
- ORDレコード
- ord-fbc0dba1edb14fd3a2d083c0adf212e0
- 出典データセット
- uspto-grants-1976_07
- 特許番号
- US03970683
反応ノート
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