Sodium Chloride → 2-Amino-3-cyano-4-methyl-5-phenylcarbonylpyridine

HRID 233611ノート

反応式

HRID 233611 の反応式
[NH2:1][C:2]1[C:7]([C:8]#[N:9])=[C:6]([CH3:10])[C:5](I)=[CH:4][N:3]=1.[C]=O.[C:14]1(B(O)O)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(N(CC)CC)C.[Cl-].[Na+].[O:32]1CCOC[CH2:33]1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O>[NH2:1][C:2]1[C:7]([C:8]#[N:9])=[C:6]([CH3:10])[C:5]([C:33]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[O:32])=[CH:4][N:3]=1

参加物

9

反応物 6

HCID 5234Sodium ChlorideHCID 8471TriethylamineHCID 312751,4-DioxaneHCID 66827Phenylboronic AcidHCID 113912652-Amino-5-iodo-4-methylnicotinonitrileHCID 178418416HCID 178418416、化合物3 回

生成物 1

HCID 197072072-Amino-3-cyano-4-methyl-5-phenylcarbonylpyridine

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒HCID 962Water溶媒

反応条件

温度
65 °C

実験手順

A solution of 4.9 grams (0.019 mole) of 2-amino-3-cyano-5-iodo-4-methylpyridine (prepared as in Step E of Example 9) in 75 mL of dioxane is stirred, and gaseous carbon monoxide is bubbled in during a 15 minute period. While maintaining a carbon monoxide atmosphere, 4.7 grams (0.039 mole) of phenylboronic acid (commercially available), 6.8 mL (0.048 mole) of triethylamine, and 0.5 gram (catalyst) of palladium(II) acetate are in turn added. To maintain the carbon monoxide atmosphere, a balloon filled with carbon monoxide gas is then attached to the reaction vessel. The reaction mixture is then warmed to 65° C. where it is stirred for about 20 hours. The reaction mixture is then poured into a mixture of 300 mL of water and 100 mL of aqueous saturated sodium chloride solution. This mixture is extracted with two 150 mL portions of ethyl acetate. The combined extracts are dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue. The residue is purified using column chromatography, yielding 2-amino-3-cyano-4-methyl-5-phenylcarbonylpyridine.

後処理

  1. customgaseous carbon monoxide is bubbled in during a 15 minute period
  2. additionadded
  3. extractionThis mixture is extracted with two 150 mL portions of ethyl acetate
  4. dry with materialThe combined extracts are dried with magnesium sulfate
  5. filtrationfiltered
  6. concentrationThe filtrate is concentrated under reduced pressure to a residue
  7. customThe residue is purified

出典と根拠

ORDレコード
ord-e7c523036a4c4054b75c258d00618734
出典データセット
uspto-grants-1997_01
特許番号
US05593998

反応ノート

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