1-Chloro-4-acetoxynonane → 7-[1-(4(R)-hydroxy-2-nonynyl)ureido]heptanoic acid
反応式
ClCCCC([O:11]C(=O)C)CCCCC.C([O:18][CH:19]([CH2:37][CH2:38][CH2:39][CH:40]=[CH2:41])[CH2:20][CH2:21][CH2:22][N:23]([CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][C:32]([O:34]CC)=[O:33])[C:24]#[N:25])(=O)C>>[OH:18][C@H:19]([CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])[C:20]#[C:21][CH2:22][N:23]([CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][C:32]([OH:34])=[O:33])[C:24]#[N:25].[OH:18][C@H:19]([CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])[C:20]#[C:21][CH2:22][N:23]([CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][C:32]([OH:34])=[O:33])[C:24]([NH2:25])=[O:11]参加物
4
実験手順
The synthesis of this compound is carried out as described in Example 1 except that, in Step A, the 1-chloro-4-acetoxynonane is replaced by an equimolar amount of 1-chloro-4-aceotoxy-8nonane. The product of Step A is thus ethyl 7-[N-(4-acetoxy-8-nonenyl)cyanamido]heptanoate. The subsequent steps yield 7-[N-(4-hydroxy-8-nonenyl)cyanamido]heptanoic acid (B) and 7-[1-(4-hydroxy-8-nonenyl)ureido]heptanoic acid (C).