Benzyl Bromide → (3S,4S)-4-(1-benzyloxycarbonylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone

HRID 1196201ノート

反応式

HRID 1196201 の反応式
[C:1]([C:4]([C@H:6]1[N:9]([CH:10]([CH2:20][C:21]2[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[CH:23][CH:22]=2)[CH2:11][C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)[C:8](=[O:29])[C@@H:7]1[C@H:30]([O:32][C:33]([O:35][CH2:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)=[O:34])[CH3:31])=[CH2:5])([OH:3])=[O:2].[CH2:43](Br)[C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH2:43]([O:2][C:1]([C:4]([C@H:6]1[N:9]([CH:10]([CH2:20][C:21]2[CH:26]=[CH:25][C:24]([O:27][CH3:28])=[CH:23][CH:22]=2)[CH2:11][C:12]2[CH:13]=[CH:14][C:15]([O:18][CH3:19])=[CH:16][CH:17]=2)[C:8](=[O:29])[C@@H:7]1[C@H:30]([O:32][C:33]([O:35][CH2:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)=[O:34])[CH3:31])=[CH2:5])=[O:3])[C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1

参加物

5

反応物 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 67919435(3S,4S)-4-(1-carboxyethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone

生成物 1

HCID 67919445(3S,4S)-4-(1-benzyloxycarbonylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A solution of (3S,4S)-4-(1-carboxyethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone (3.7 g) in acetone (60 ml) was treated with benzyl bromide (1.4 g) in the presence of anhydrous potassium carbonate (1.88 g) under reflux for 2 hours. The reaction mixture was cooled down to room temperature, filtered to remove insoluble materials and concentrated in vacuo. The concentrate was diluted with ethyl acetate, washed with water and dried over anhydrous sodium sulfate. Filtration and concentration of the filtrate in vacuo gave (3S,4S)-4-(1-benzyloxycarbonylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone.

後処理

  1. temperatureunder reflux for 2 hours
  2. filtrationfiltered
  3. customto remove insoluble materials
  4. concentrationconcentrated in vacuo
  5. additionThe concentrate was diluted with ethyl acetate
  6. washwashed with water
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationFiltration and concentration of the filtrate in vacuo

出典と根拠

ORDレコード
ord-8fecda6a72b14d9386f34fc2b6e0e354
出典データセット
uspto-grants-1992_05
特許番号
US05112966

反応ノート

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