Phosphate → (R)-N,N-diisopropyl-3-(5-formyl-2-hydroxyphenyl)-3-phenylpropanamine
反応式
C(C1C(=O)C(Cl)=C(Cl)C(=O)C=1C#N)#N.C(O)(=O)C(C1C=CC=CC=1)O.[CH:26]([N:29]([CH:48]([CH3:50])[CH3:49])[CH2:30][CH2:31][C@@H:32]([C:39]1[CH:44]=[C:43]([CH2:45][OH:46])[CH:42]=[CH:41][C:40]=1[OH:47])[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)([CH3:28])[CH3:27].P([O-])([O-])([O-])=O.[OH-].[Na+]>C(OCC)C.ClCCl>[CH:48]([N:29]([CH:26]([CH3:28])[CH3:27])[CH2:30][CH2:31][C@@H:32]([C:39]1[CH:44]=[C:43]([CH:45]=[O:46])[CH:42]=[CH:41][C:40]=1[OH:47])[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)([CH3:50])[CH3:49]参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
DDQ (1.1 eq) was added to a solution of (R)-N,N-diisopropyl-3-(2-hydroxy-5-hydroxymethylphenyl)-3-phenylpropanamine mandelate (prepared as described in WO 94/11337, Example 1) (2.46 g, 5 mmol), dichloromethane (20 mL) and phosphate buffer (pH 7) (0.1 mL). Thereafter, sodium hydroxide solution (20 mL, 1 M) and diethyl ether were added and the phases were separated. The water-phase was extracted twice with dichloromethane-diethyl ether (2:1). The organic phase was dried (MgSO4) and evaporated. The residue was crystallised from ethyl acetate-hexane to yield 1.35 g (80%).
後処理
- customthe phases were separated
- extractionThe water-phase was extracted twice with dichloromethane-diethyl ether (2:1)
- dry with materialThe organic phase was dried (MgSO4)
- customevaporated
- customThe residue was crystallised from ethyl acetate-hexane
- customto yield 1.35 g (80%)
出典と根拠
- ORDレコード
- ord-2a05ebd6ff974fb7a59d5a7b8fea72f0
- 出典データセット
- uspto-grants-2001_11
- 特許番号
- US06313132B1
反応ノート
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