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Cesium carbonate → Ethyl rac-2-[3-(4-chlorophenyl)-4-cyclopropyl-5-oxo-4,5-dihydro-1h-1,2,4-triazol-1-yl]propionate

HRID 660857
ノート
印刷プレビュー

反応式

HRID 660857 の反応式
Br[CH:2]([CH3:8])[C:3]([O:5][CH2:6][CH3:7])=[O:4].C(=O)([O-])[O-].[Cs+].[Cs+].[Cl:15][C:16]1[CH:21]=[CH:20][C:19]([C:22]2[N:23]([CH:28]3[CH2:30][CH2:29]3)[C:24](=[O:27])[NH:25][N:26]=2)=[CH:18][CH:17]=1>C(#N)C>[Cl:15][C:16]1[CH:17]=[CH:18][C:19]([C:22]2[N:23]([CH:28]3[CH2:29][CH2:30]3)[C:24](=[O:27])[N:25]([CH:2]([CH3:8])[C:3]([O:5][CH2:6][CH3:7])=[O:4])[N:26]=2)=[CH:20][CH:21]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 10796Cesium carbonateHCID 79040Ethyl 2-bromopropionateHCID 580121993-(4-Chlorophenyl)-4-cyclopropyl-1H-1,2,4-triazol-5(4H)-one

生成物 1

HCID 58012037Ethyl rac-2-[3-(4-chlorophenyl)-4-cyclopropyl-5-oxo-4,5-dihydro-1h-1,2,4-triazol-1-yl]propionate

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
85 °C

実験手順

384 mg (2.12 mmol) of ethyl 2-bromopropionate and 1.38 g (4.24 mmol) of caesium carbonate are added to 500 mg (2.12 mmol) of 5-(4-chlorophenyl)-4-cyclopropyl-2,4-dihydro-3H-1,2,4-triazol-3-one from Example 36A in 5 ml acetonitrile and the reaction mixture is heated at 85° C. overnight. It is then concentrated in vacuo, the residue is partitioned between water and dichloromethane, and the separated organic phase is dried over sodium sulphate and again evaporated. After purification of the residue by flash chromatography over silica gel (eluent: first dichloromethane, then dichloromethane/methanol 200:1), 729 mg (97% of theory) of the target compound are obtained.

後処理

  1. concentrationIt is then concentrated in vacuo
  2. customthe residue is partitioned between water and dichloromethane
  3. dry with materialthe separated organic phase is dried over sodium sulphate
  4. customagain evaporated
  5. customAfter purification of the residue by flash chromatography over silica gel (eluent
  6. customfirst dichloromethane, then dichloromethane/methanol 200:1), 729 mg (97% of theory) of the target compound are obtained

出典と根拠

ORDレコード
ord-33b5651bcaa24a30bbe7abb571a57d20
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08084481B2

反応ノート

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