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Dimethylformamide → 2-[1-(4-amino-3-nitrophenyl)ethenyl]-N-[3-(trifluoromethyl)phenyl]benzamide

HRID 2261964
ノート
印刷プレビュー

反応式

HRID 2261964 の反応式
Cl[C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:10]2[CH:28]=[CH:27][CH:26]=[CH:25][C:11]=2[C:12]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([C:21]([F:24])([F:23])[F:22])[CH:16]=2)=[O:13])=[CH2:9])=[CH:4][C:3]=1[N+:29]([O-:31])=[O:30].[N-:32]=[N+]=[N-].[Na+].CN(C)C=O.[BH4-].[Na+]>C(OCC)(=O)C.O1CCCC1>[NH2:32][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:10]2[CH:28]=[CH:27][CH:26]=[CH:25][C:11]=2[C:12]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([C:21]([F:24])([F:23])[F:22])[CH:16]=2)=[O:13])=[CH2:9])=[CH:4][C:3]=1[N+:29]([O-:31])=[O:30]
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

7

反応物 4

HCID 6228DimethylformamideHCID 33557Sodium AzideHCID 4311764Sodium borohydrideHCID 67045429HCID 67045429、化合物

生成物 1

HCID 670444852-[1-(4-amino-3-nitrophenyl)ethenyl]-N-[3-(trifluoromethyl)phenyl]benzamide収率 50%

試薬・触媒・溶媒 2

HCID 8028
Tetrahydrofuran
溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
60 °C

実験手順

A mixture of 2-[1-(4-chloro-3-nitrophenyl)ethenyl]-N-[3-(trifluoromethyl)phenyl]benzamide (0.72 g, 1.6 mmol), sodium azide (3.1 g, 4.8 mmol) and N,N-dimethylformamide (2 mL) was stirred 60° C. for 18 hours. The reaction mixture was diluted with ethyl acetate (50 mL), washed with water (3×30 mL), brine (30 mL), dried over sodium sulfate, filtered and concentrated to give an oily residue. This residue was dissolved in tetrahydrofuran, cooled to 0° C. then sodium borohydride (0.11 g, 2.7 mmol) was added and stirring was continued for 30 minutes at room temperature. The reaction mixture was quenched with methanol (2 mL), concentrated then diluted with ethyl acetate (50 mL). The organic solution was washed with water (30 mL) then brine solution (30 mL) then dried over sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography (silica gel, eluting with 15-50% ethyl acetate-hexane) to give 2-[1-(4-amino-3-nitrophenyl)ethenyl]-N-[3-(trifluoromethyl)phenyl]benzamide (0.35 g, 0.8 mmol, 50% yield). MS (EI) for C22H16F3N3O3: 428 (MH+).

後処理

  1. washwashed with water (3×30 mL), brine (30 mL)
  2. dry with materialdried over sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customto give an oily residue
  6. temperaturecooled to 0° C.
  7. stirringstirring
  8. waitwas continued for 30 minutes at room temperature
  9. customThe reaction mixture was quenched with methanol (2 mL)
  10. concentrationconcentrated
  11. additionthen diluted with ethyl acetate (50 mL)
  12. washThe organic solution was washed with water (30 mL)
  13. dry with materialbrine solution (30 mL) then dried over sodium sulfate
  14. filtrationfiltered
  15. concentrationconcentrated
  16. customThe residue was purified by flash chromatography (silica gel, eluting with 15-50% ethyl acetate-hexane)

出典と根拠

ORDレコード
ord-35e1c3c670434e169dc83b35f4289a1f
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07846959B2

反応ノート

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