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Methyl 2,2,2-trichloroacetimidate → 6-fluoro-1-(4-methoxybutyl)-2-(trichloromethyl)-1H-benzimidazole

HRID 1259911
ノート
印刷プレビュー

反応式

HRID 1259911 の反応式
[F:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([NH:9][CH2:10][CH2:11][CH2:12][CH2:13][O:14][CH3:15])[CH:3]=1.[Cl:16][C:17]([Cl:23])([Cl:22])[C:18](=N)OC>C(O)(=O)C>[F:1][C:2]1[CH:8]=[CH:7][C:5]2[N:6]=[C:18]([C:17]([Cl:23])([Cl:22])[Cl:16])[N:9]([CH2:10][CH2:11][CH2:12][CH2:13][O:14][CH3:15])[C:4]=2[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 100479Methyl 2,2,2-trichloroacetimidateHCID 583555474-Fluoro-2-(4-methoxybutylamino)aniline

生成物 1

HCID 583553976-fluoro-1-(4-methoxybutyl)-2-(trichloromethyl)-1H-benzimidazole

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

4-Fluoro-2-(4-methoxybutylamino)aniline (4.28 g) was dissolved in acetic acid (100 ml), methyl 2,2,2-trichloroethanimidate (2.49 ml) was added dropwise, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, and the residue was azeotroped with toluene. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate was concentrated under reduced pressure to give the object product (6.53 g).

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customthe residue was azeotroped with toluene
  3. washa fraction eluted with ethyl acetate
  4. concentrationwas concentrated under reduced pressure

出典と根拠

ORDレコード
ord-83f1d3f08eae456e99540787c04071f0
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08466282B2

反応ノート

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