Dimethyl Sulfoxide → 4-(5-Bromo-2-pyrimidinyloxy)-3-chloroaniline

HRID 4512

反応式

HRID 4512 の反応式
[Br:1][C:2]1[CH:3]=[N:4][C:5](Cl)=[N:6][CH:7]=1.[NH2:9][C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[C:12]([Cl:17])[CH:11]=1.C(=O)([O-])[O-].[K+].[K+].CS(C)=O>O>[Br:1][C:2]1[CH:3]=[N:4][C:5]([O:16][C:13]2[CH:14]=[CH:15][C:10]([NH2:9])=[CH:11][C:12]=2[Cl:17])=[N:6][CH:7]=1

参加物

6

反応物 4

HCID 679Dimethyl SulfoxideHCID 11430Potassium CarbonateHCID 775784-Amino-2-chlorophenolHCID 6066655-Bromo-2-chloropyrimidine

生成物 1

HCID 137714404-(5-Bromo-2-pyrimidinyloxy)-3-chloroaniline収率 62.6%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Into a flask, 7.00 g of 5-bromo-2-chloropyrimidine, 5.19 g of 4-amino-2-chlorophenol, 9.98 g of potassium carbonate and 70 ml of dimethylsulfoxide were introduced, and reacted in a nitrogen atmosphere at 120° C. for 1.5 hours under stirring. After the completion of the reaction, the product was poured into water, and extracted with ethyl acetate. The extract was washed with water and a saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate, and then purified by silica gel column chromatography, whereby 6.80 g of oily 4-(5-bromo-2-pyrimidinyloxy)-3-chloroaniline was obtained.

後処理

  1. customreacted in a nitrogen atmosphere at 120° C. for 1.5 hours
  2. customAfter the completion of the reaction
  3. extractionextracted with ethyl acetate
  4. washThe extract was washed with water
  5. dry with materiala saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate
  6. custompurified by silica gel column chromatography

出典と根拠

ORDレコード
ord-21579b9c6dbe424cb126459426052c6c
出典データセット
uspto-grants-1988_02
特許番号
US04727077

関連ノート

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