Triphenylphosphine → 1-Tert-butoxycarbonyl-4-(3-chlorophenyl)-2(s)-[2-(2-cyano-5-methoxycarbonylphenoxy)ethyl]-5-oxo-piperazine

HRID 379027ノート

反応式

HRID 379027 の反応式
[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][C:4]=1[OH:13])#[N:2].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[C:33]([O:37][C:38]([N:40]1[CH2:45][C:44](=[O:46])[N:43]([C:47]2[CH:52]=[CH:51][CH:50]=[C:49]([Cl:53])[CH:48]=2)[CH2:42][C@@H:41]1[CH2:54][CH2:55]O)=[O:39])([CH3:36])([CH3:35])[CH3:34].CCOC(/N=N/C(OCC)=O)=O>C1COCC1.CCCCCC.CCOC(C)=O>[C:33]([O:37][C:38]([N:40]1[CH2:45][C:44](=[O:46])[N:43]([C:47]2[CH:52]=[CH:51][CH:50]=[C:49]([Cl:53])[CH:48]=2)[CH2:42][C@@H:41]1[CH2:54][CH2:55][O:13][C:4]1[CH:5]=[C:6]([C:7]([O:9][CH3:10])=[O:8])[CH:11]=[CH:12][C:3]=1[C:1]#[N:2])=[O:39])([CH3:36])([CH3:35])[CH3:34]

参加物

7

実験手順

To a solution of 250 mg of methyl 4-cyano-3-hydroxybenzoate (1.42 mmol), as described in Example 4, Step C, and PPh3 (465 mg, 1.77 mmol) in THF (10 mL) was added dropwise a solution of the alcohol from Step E above (503 mg, 1.42 mmol) and DEAD (0.28 mL, 1.77 mmol) in THF (5 mL). After stirring for 16 hr, the solution was concentrated in vacuo and the residue taken up in EtOAc. This was then washed with 10% citric acid solution, saturated NaHCO3 solution, brine and dried over MgSO4. Filtration and removal of the solvent afforded an oil. Column chromatography (silica gel; hexane:EtOAc 4:1) afforded the title compound as a clear oil.

後処理

  1. concentrationthe solution was concentrated in vacuo
  2. washThis was then washed with 10% citric acid solution, saturated NaHCO3 solution, brine
  3. dry with materialdried over MgSO4
  4. filtrationFiltration and removal of the solvent
  5. customafforded an oil

出典と根拠

ORDレコード
ord-803ee359b31a40149f696cffb6d8027a
出典データセット
uspto-grants-2001_10
特許番号
US06297239B1

反応ノート

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