4-(Cyanomethyl)benzoyl chloride → 2-(4-Cyanomethylphenyl)oxazolo[5,4-b]pyridine

HRID 66382ノート

反応式

HRID 66382 の反応式
[NH2:1][C:2]1[C:3]([OH:8])=[N:4][CH:5]=[CH:6][CH:7]=1.[C:9]([CH2:11][C:12]1[CH:20]=[CH:19][C:15]([C:16](Cl)=O)=[CH:14][CH:13]=1)#[N:10]>N1C=CC=CC=1>[C:9]([CH2:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]2[O:8][C:3]3[C:2]([N:1]=2)=[CH:7][CH:6]=[CH:5][N:4]=3)=[CH:14][CH:13]=1)#[N:10]

参加物

4

反応物 2

HCID 128039484-(Cyanomethyl)benzoyl chlorideHCID 178418824HCID 178418824、化合物

生成物 1

HCID 227547692-(4-Cyanomethylphenyl)oxazolo[5,4-b]pyridine

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

Ten grams of 4-(cyanomethyl)benzoic acid is refluxed in 70 mls. of thionyl chloride for four hours. The solvents are removed leaving a residue of 4-cyanomethylbenzoyl chloride. To a solution of 5.5 g. of 3-amino-2-hydroxy pyridine in cold pyridine there is added slowly, with cooling, 8 g. of 4-cyanomethyl benzoyl chloride. The mixture is allowed to come to room temperature and stirred overnight. The mixture is added to 300 ml. of ice and the solid amide separated by filtration and recrystallized from methanol. A mixture of 3 g. of the above amide in 50 mls. of phsophorus oxychloride is heated under reflux for 5 hours. The solvents are removed in vacuo and the residue is crystallized from ethyl acetate to give 2-(4-cyanomethylphenyl)oxazolo[5,4-b]pyridine.

後処理

  1. temperaturewith cooling
  2. customto come to room temperature
  3. additionThe mixture is added to 300 ml
  4. customof ice and the solid amide separated by filtration
  5. customrecrystallized from methanol
  6. additionA mixture of 3 g
  7. temperatureof phsophorus oxychloride is heated
  8. temperatureunder reflux for 5 hours
  9. customThe solvents are removed in vacuo
  10. customthe residue is crystallized from ethyl acetate

出典と根拠

ORDレコード
ord-ace18b2d8b794fb888454a36f902365c
出典データセット
uspto-grants-1978_12
特許番号
US04131677

反応ノート

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