Dimethylformamide → 4-(1-Ethyl-propylamino)-6-methyl-2-(2,4,6-trimethyl-phenylamino)-nicotinic acid methyl ester

HRID 1245739

反応式

HRID 1245739 の反応式
[CH3:1][O:2][C:3](=[O:18])[C:4]1[C:9]([NH:10][CH:11]([CH2:14][CH3:15])[CH2:12][CH3:13])=[CH:8][C:7]([CH3:16])=[N:6][C:5]=1Cl.[CH3:19][C:20]1[CH:28]=[CH:27][CH:26]=[CH:25][C:21]=1N(C)C.[C:29](=O)([O-])[O-].[K+].[K+].C[N:36]([CH:38]=O)C>[Cu]>[CH3:1][O:2][C:3](=[O:18])[C:4]1[C:9]([NH:10][CH:11]([CH2:14][CH3:15])[CH2:12][CH3:13])=[CH:8][C:7]([CH3:16])=[N:6][C:5]=1[NH:36][C:38]1[C:25]([CH3:21])=[CH:26][C:27]([CH3:29])=[CH:28][C:20]=1[CH3:19]

参加物

6

実験手順

A mixture of 2-chloro-4-(1-ethyl-propylamino)-6-methyl-nicotinic acid methyl ester, trimethylaniline, potassium carbonate, copper in DMF was heated at reflux. The mixture was quenched with ammonium chloride and stirred for 20 min, filtered through celite and washed with ethyl acetate. The filtrate was extracted with ethyl acetate. The organic layer was separated, dried and concentrated to dryness. The residue was purified through silica gel column chromatography using 2% methanol in chloroform as eluent to give the title compound as a solid.

後処理

  1. temperaturewas heated
  2. temperatureat reflux
  3. customThe mixture was quenched with ammonium chloride
  4. filtrationfiltered through celite
  5. washwashed with ethyl acetate
  6. extractionThe filtrate was extracted with ethyl acetate
  7. customThe organic layer was separated
  8. customdried
  9. concentrationconcentrated to dryness
  10. customThe residue was purified through silica gel column chromatography

出典と根拠

ORDレコード
ord-4f03e17beaa84580b5c35b5b6b64d128
出典データセット
uspto-grants-2006_10
特許番号
US07125880B1

関連ノート

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