Dimethylformamide → 6-(2,6-Dichlorophenyl)-8-methyl-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-imine

HRID 53629

反応式

HRID 53629 の反応式
C(=O)([O-])[O-].[K+].[K+].[CH3:7][NH:8][C:9]1[C:14]([CH:15]=O)=[CH:13][N:12]=[C:11]([S:17][CH3:18])[N:10]=1.[Cl:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([Cl:26])[C:21]=1CC#N.C(O[CH2:34][CH3:35])(=O)C.C[N:37](C)C=O>C(Cl)Cl>[Cl:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([Cl:26])[C:21]=1[C:35]1[C:34](=[NH:37])[N:8]([CH3:7])[C:9]2[N:10]=[C:11]([S:17][CH3:18])[N:12]=[CH:13][C:14]=2[CH:15]=1

参加物

7

反応物 5

HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 76678(2,6-Dichlorophenyl)acetonitrileHCID 106075204-(Methylamino)-2-(methylthio)pyrimidine-5-carbaldehyde

生成物 1

HCID 108078276-(2,6-Dichlorophenyl)-8-methyl-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-imine収率 40%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
125 °C

実験手順

Powdered potassium carbonate (0.8 g; 5.8 mmol) was added to a solution of 0.220 g (1.2 mmol) of the aldehyde from Example 18 and 0.235 g (1.26 mmol) (ca. 5% excess) of 2,6-dichlorophenylacetonitrile in 2.0 mL of dimethylformamide. The mixture was heated with stirring at 125° C. for 6 hours. Ethyl acetate (5 mL) was added to the cooled mixture, and the solids were filtered and washed with ethyl acetate. The filtrate was concentrated under reduced pressure. The residual gum was triturated with 10 mL of water, and the resulting solid was filtered, washed well with water, and dried. This crude material was chromatographed by placing a chloroform solution on a silica gel column wet with chloroform. The column was eluted with 1:1 (v/v) hexane:ethyl acetate, collecting the fractions that contain the Rf 0.25 spot on tlc (1:1 hexane:ethyl acetate). Evaporation of the solvents gave a solid. The solid product was dissolved in about 0.5 mL of methylene chloride. Crystals develop. Petroleum ether (ca. 2 mL) was added, and the crystals were filtered to provide 0.168 g (40%) of 6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-ylideneamine, mp 198°-200° C.;

後処理

  1. temperatureThe mixture was heated
  2. filtrationthe solids were filtered
  3. washwashed with ethyl acetate
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. customThe residual gum was triturated with 10 mL of water
  6. filtrationthe resulting solid was filtered
  7. washwashed well with water
  8. customdried
  9. customThis crude material was chromatographed
  10. washThe column was eluted with 1:1 (v/v) hexane
  11. customethyl acetate, collecting the fractions that
  12. customEvaporation of the solvents
  13. customgave a solid
  14. filtrationthe crystals were filtered

出典と根拠

ORDレコード
ord-3c1ba819d1914d3589c7b7c92e2c4cb5
出典データセット
uspto-grants-1997_04
特許番号
US05620981

関連ノート

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