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({3-Bromo-5-cyano-2-[(trifluoroacetyl)amino]phenyl}methyl)(triphenyl)phosphonium bromide → HCID 58138925、化合物

HRID 2061565
ノート
印刷プレビュー

反応式

HRID 2061565 の反応式
[Br-].[Br:2][C:3]1[C:4]([NH:31][C:32](=O)[C:33]([F:36])([F:35])[F:34])=[C:5]([CH2:11][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH:6]=[C:7]([C:9]#[N:10])[CH:8]=1>CN(C=O)C>[CH3:8][CH2:3][CH2:4][CH:5]([CH3:11])[CH3:6].[F:34][C:33]([F:36])([F:35])[C:32]1[NH:31][C:4]2[C:5]([CH:11]=1)=[CH:6][C:7]([C:9]#[N:10])=[CH:8][C:3]=2[Br:2]
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

4

反応物 1

HCID 86650874({3-Bromo-5-cyano-2-[(trifluoroacetyl)amino]phenyl}methyl)(triphenyl)phosphonium bromide

生成物 2

HCID 78922-MethylpentaneHCID 58138925HCID 58138925、化合物収率 72.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
130 °C

実験手順

({3-bromo-5-cyano-2-[(trifluoroacetyl)amino]phenyl}methyl)(triphenyl)phosphonium bromide (37.2 g, crude) was dissolved in DMF (150 mL) and the reaction mixture was heated to 130° C. stirring for 3 hrs. The reaction mixture was allowed to cool to room temperature then quenched with water (400 mL). The reaction mixture was then extracted with ethyl acetate (3×300 mL). The organic extract was washed with a 1:1 mixture of water:brine (2×600 mL), dried (MgSO4), filtered and the solvent was removed. The resulting residues were then purified by filtration through a pad of silica gel eluting with 2-10% EtOAc: isoHexane to give the title compound as an off-white solid (6 g);

後処理

  1. temperatureto cool to room temperature
  2. customthen quenched with water (400 mL)
  3. extractionThe reaction mixture was then extracted with ethyl acetate (3×300 mL)
  4. extractionThe organic extract
  5. washwas washed with a 1:1 mixture of water
  6. dry with materialbrine (2×600 mL), dried (MgSO4)
  7. filtrationfiltered
  8. customthe solvent was removed
  9. filtrationThe resulting residues were then purified by filtration through a pad of silica gel eluting with 2-10% EtOAc

出典と根拠

ORDレコード
ord-7f7d816a05964bc3846d156e39c71d2c
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08283365B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート