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Sodium Iodide → N-{[4-(3,4Dichlorobenzyl)morpholin-2-yl]methyl}-2,2,2-trifluoroacetamide

HRID 2211982
ノート
印刷プレビュー

反応式

HRID 2211982 の反応式
[F:1][C:2]([F:14])([F:13])[C:3]([NH:5][CH2:6][CH:7]1[O:12][CH2:11][CH2:10][NH:9][CH2:8]1)=[O:4].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+].[Cl:23][C:24]1[CH:25]=[C:26]([CH:29]=[CH:30][C:31]=1[Cl:32])[CH2:27]Cl>CN(C)C=O>[Cl:23][C:24]1[CH:25]=[C:26]([CH:29]=[CH:30][C:31]=1[Cl:32])[CH2:27][N:9]1[CH2:10][CH2:11][O:12][CH:7]([CH2:6][NH:5][C:3](=[O:4])[C:2]([F:13])([F:1])[F:14])[CH2:8]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

6

反応物 4

HCID 5238Sodium IodideHCID 76093,4-Dichlorobenzyl chlorideHCID 11430Potassium CarbonateHCID 115502612,2,2-trifluoro-N-(morpholin-2-ylmethyl)acetamide

生成物 1

HCID 11588781N-{[4-(3,4Dichlorobenzyl)morpholin-2-yl]methyl}-2,2,2-trifluoroacetamide

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒
2 回

反応条件

温度
22 °C

実験手順

To a stirred solution of Intermediate 19 (3.3 g) in N,N-dimethylformamide (50 ml) under nitrogen was added potassium carbonate (2.46 g) and sodium iodide (2.12 g). A solution of 3,4-dichlorobenzyl chloride (2 ml) in N,N-dimethylformamide (10 ml) was added dropwise to the mixture. The mixture was stirred at 22° C. for 18 h before the volatiles were removed in vacuo. The residue was partitioned between dichloromethane (100 ml) and saturated aqueous sodium carbonate solution (50 ml). The organic phase was subsequently washed with additional saturated aqueous sodium carbonate solution (2×50 ml) and water (50 ml) before drying over magnesium sulphate, filtering and evaporation of the solventin vacuo to give a pale yellow oil. The oil was purified by Biotage flash chromatography on a 90 g silica cartridge eluting with 25% ethyl acetate in cyclohexane, to give the title compound as a colourless oil (2.97 g).

後処理

  1. customwere removed in vacuo
  2. customThe residue was partitioned between dichloromethane (100 ml) and saturated aqueous sodium carbonate solution (50 ml)
  3. washThe organic phase was subsequently washed with additional saturated aqueous sodium carbonate solution (2×50 ml) and water (50 ml)
  4. dry with materialbefore drying over magnesium sulphate
  5. filtrationfiltering
  6. customevaporation of the solventin vacuo
  7. customto give a pale yellow oil
  8. customThe oil was purified by Biotage flash chromatography on a 90 g silica cartridge
  9. washeluting with 25% ethyl acetate in cyclohexane

出典と根拠

ORDレコード
ord-971e8fae592b4639a3a8c7c6bb81612f
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07101882B2

反応ノート

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