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Ethyl chloroformate → N-(1-(4-((4-(4-fluorophenyl)piperazin-1-yl)methyl)phenyl)cyclopropyl)acetamide

HRID 1282111
ノート
印刷プレビュー

反応式

HRID 1282111 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH2:14][C:15]3[CH:20]=[CH:19][C:18]([C:21]4(C(O)=O)[CH2:23][CH2:22]4)=[CH:17][CH:16]=3)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.C(Cl)(=O)[O:28][CH2:29][CH3:30].[N-:33]=[N+]=[N-].[Na+].C[Mg]I.[Cl-].[NH4+]>O.CC(C)=O.C1(C)C=CC=CC=1.C(N(CC)CC)C>[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:9][CH2:10][N:11]([CH2:14][C:15]3[CH:20]=[CH:19][C:18]([C:21]4([NH:33][C:29](=[O:28])[CH3:30])[CH2:22][CH2:23]4)=[CH:17][CH:16]=3)[CH2:12][CH2:13]2)=[CH:4][CH:3]=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

10

反応物 5

HCID 10928Ethyl chloroformateHCID 25517Ammonium ChlorideHCID 33557Sodium AzideHCID 184230631-(4-((4-(4-Fluorophenyl)piperazin-1-yl)methyl)phenyl)cyclopropanecarboxylic acidHCID 178418373HCID 178418373、化合物

生成物 1

HCID 11523509N-(1-(4-((4-(4-fluorophenyl)piperazin-1-yl)methyl)phenyl)cyclopropyl)acetamide

試薬・触媒・溶媒 4

HCID 180Acetone溶媒3 回HCID 962Water溶媒2 回HCID 1140Toluene溶媒HCID 8471Triethylamine溶媒

反応条件

温度
0 °C

実験手順

To a suspension of 1-(4-((4-(4-fluorophenyl)piperazin-1-yl)methyl)phenyl)cyclopropanecarboxylic acid (1.73 g) in water (1.7 ml) was added acetone (7 ml) and dissolved therein. A solution of triethylamine (0.75 ml) in acetone (10 ml) was added under ice-cooling and a solution of ethyl chlorocarbonate (0.56 ml) in acetone (4 ml) was added dropwise over 15 min. The mixture was stirred at 0° C. for 30 min. To this solution was added dropwise a solution of sodium azide (0.48 g) in water (3 ml) under ice-cooling over 10 min. The mixture was stirred for 30 min. The reaction mixture was poured into ice water (100 ml) and extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate and the solvent was evaporated to give an oil. The oil was dissolved in toluene (17 ml) and heated at 100° C. for 1 hr. The reaction mixture was ice-cooled and methylmagnesium iodide (1M, diethyl ether solution) (4.3 ml) was added. The mixture was stirred at room temperature for 30 min. The reaction mixture was poured into aqueous ammonium chloride and extracted with water and ethyl acetate (100 ml). The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated and the obtained residue was purified by silica gel column chromatography (developing solvent; ethyl acetate:methanol=100:1) and recrystallized from ethyl acetate-isopropyl ether to give the title compound (0.52 g) as white crystals.

後処理

  1. dissolutiondissolved
  2. temperaturecooling
  3. temperaturecooling over 10 min
  4. stirringThe mixture was stirred for 30 min
  5. extractionextracted with diethyl ether
  6. dry with materialThe extract was dried over anhydrous magnesium sulfate
  7. customthe solvent was evaporated
  8. customto give an oil
  9. temperatureheated at 100° C. for 1 hr
  10. temperaturecooled
  11. stirringThe mixture was stirred at room temperature for 30 min
  12. extractionextracted with water and ethyl acetate (100 ml)
  13. washThe extract was washed with saturated brine
  14. dry with materialdried over anhydrous magnesium sulfate
  15. customThe solvent was evaporated
  16. customthe obtained residue was purified by silica gel column chromatography (developing solvent; ethyl acetate:methanol=100:1)
  17. customrecrystallized from ethyl acetate-isopropyl ether

出典と根拠

ORDレコード
ord-b949882a28764547b3e61d21bee38303
出典データセット
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06455528B1

反応ノート

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