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Dimethylformamide → HCID 89690426、化合物

HRID 1481858
ノート
印刷プレビュー

反応式

HRID 1481858 の反応式
[C:1](=O)([O-])[O-].[K+].[K+].CN(C)C=O.[Cl:12][C:13]1[CH:21]=[C:20]([N:22]2[CH2:27][CH2:26][N:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[CH3:34])[CH2:24][CH2:23]2)[C:19]([N+:35]([O-:37])=[O:36])=[CH:18][C:14]=1[C:15]([OH:17])=[O:16].IC>O>[CH3:1][O:16][C:15](=[O:17])[C:14]1[CH:18]=[C:19]([N+:35]([O-:37])=[O:36])[C:20]([N:22]2[CH2:27][CH2:26][N:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[CH3:34])[CH2:24][CH2:23]2)=[CH:21][C:13]=1[Cl:12]
参加物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 6228DimethylformamideHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 89690510HCID 89690510、化合物

生成物 1

HCID 89690426HCID 89690426、化合物収率 92.8%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

In a 250 ml round bottom flask equipped with a magnetic stir bar, the potassium carbonate (2.06 g, 14.91 mmol) was suspended in clean, dry N,N-dimethylformamide (50.00 ml, 645.74 mmol) and the mixture was stirred together under nitrogen at room temperature as the 2-chloro-5-nitro-4-(4-o-tolyl-piperazin-1-yl)-benzoic acid 1d (2.54 g, 6.76 mmol) was added in one portion. The mixture was stirred until it appeared all the organic solids were in solution and then iodomethane (0.46 ml, 7.39 mmol) was added. The reaction was diluted with 100 ml of water and the product was extracted from the aqueous using ethyl acetate (3×100 ml). The layers were separated and the organic phases were combined, washed with brine (1×150 ml) and saturated aqueous lithium chloride solution (2×150 ml). The solution was then dried over Na2SO4; the solution was decanted and the solvent was removed under reduced pressure. The compound was purified using silica gel column chromatography, eluting a gradient of 100% heptanes to 75% ethyl acetate in heptane. 2-Chloro-5-nitro-4-(4-o-tolyl-piperazin-1-yl)-benzoic acid methyl ester 10a (2.45 g, 6.27 mmol) was isolated as a yellowish-white solid and was carried on without further purification. LCMS (m/e)=390 (M+H).

後処理

  1. customIn a 250 ml round bottom flask equipped with a magnetic stir bar
  2. additionwas added in one portion
  3. extractionthe product was extracted from the
  4. customThe layers were separated
  5. washwashed with brine (1×150 ml) and saturated aqueous lithium chloride solution (2×150 ml)
  6. dry with materialThe solution was then dried over Na2SO4
  7. customthe solution was decanted
  8. customthe solvent was removed under reduced pressure
  9. customThe compound was purified
  10. washeluting a gradient of 100% heptanes to 75% ethyl acetate in heptane

出典と根拠

ORDレコード
ord-95e118dec870468eaa07a70d7e9cd5cc
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409897B2

反応ノート

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