Lithium Hydroxide → (E)-(3S,8aR)-3-(4-chlorophenyl)-6-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene]hexahydroindolizin-5-one

HRID 16345ノート

反応式

HRID 16345 の反応式
[OH-].[Li+].O1CCCC1.[CH3:8][O:9][C:10]1[CH:11]=[C:12]([CH:15]=[CH:16][C:17]=1[N:18]1[CH:22]=[C:21]([CH3:23])[N:20]=[CH:19]1)[CH:13]=O.C(OP([CH:32]1[CH2:40][CH2:39][C@@H:38]2[N:34]([C@H:35]([C:41]3[CH:46]=[CH:45][C:44]([Cl:47])=[CH:43][CH:42]=3)[CH2:36][CH2:37]2)[C:33]1=[O:48])(=O)OCC)C>O.C(O)C>[Cl:47][C:44]1[CH:43]=[CH:42][C:41]([C@H:35]2[N:34]3[C@H:38]([CH2:39][CH2:40]/[C:32](=[CH:13]\[C:12]4[CH:15]=[CH:16][C:17]([N:18]5[CH:22]=[C:21]([CH3:23])[N:20]=[CH:19]5)=[C:10]([O:9][CH3:8])[CH:11]=4)/[C:33]3=[O:48])[CH2:37][CH2:36]2)=[CH:46][CH:45]=1

参加物

7

反応物 4

HCID 3939Lithium HydroxideHCID 8028TetrahydrofuranHCID 272824453-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehydeHCID 86612704diethyl[(3S,8aR)-3-(4-chlorophenyl)-5-oxooctahydroindolizin-6-yl]phosphonate

生成物 1

HCID 68717808(E)-(3S,8aR)-3-(4-chlorophenyl)-6-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene]hexahydroindolizin-5-one収率 78.9%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

Lithium hydroxide (355 mg) was added to a solution mixture of tetrahydrofuran (8 mL)-ethanol (30 mL) of 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde (875 mg) and [(3S,8aR)-3-(4-chlorophenyl)-5-oxooctahydroindolizin-6-yl]phosphonic acid diethyl ester (2.5 g). The resulting reaction solution was stirred under light-shielded conditions at room temperature for 5 hr and then poured into iced-water. The resulting mixture was extracted with ethyl acetate. The extract solution was washed with saturated saline, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane-ethyl acetate system) to give 1.43 g of the title compound as a colorless solid. The physical property values of this compound were as follows:

後処理

  1. customThe resulting reaction solution
  2. extractionThe resulting mixture was extracted with ethyl acetate
  3. washThe extract solution was washed with saturated saline
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (heptane-ethyl acetate system)

出典と根拠

ORDレコード
ord-fba512a2cdc34ccb9e41ce6e0adba248
出典データセット
uspto-grants-2010_06
特許番号
US07737141B2

反応ノート

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