Triethylamine → 6-Chloro-3-(2,6-difluorophenyl)-[1,2,4]triazine

HRID 2085922ノート

反応式

HRID 2085922 の反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[C:9]1[N:14]=[CH:13][C:12](=O)[NH:11][N:10]=1.O=P(Cl)(Cl)[Cl:18].C(N(CC)CC)C>O1CCOCC1>[Cl:18][C:12]1[N:11]=[N:10][C:9]([C:3]2[C:2]([F:1])=[CH:7][CH:6]=[CH:5][C:4]=2[F:8])=[N:14][CH:13]=1

参加物

5

反応物 3

HCID 8471TriethylamineHCID 24813Phosphorus oxychlorideHCID 227270193-(2,6-difluorophenyl)-[1,2,4]triazin-6(1H)-one

生成物 1

HCID 227270216-Chloro-3-(2,6-difluorophenyl)-[1,2,4]triazine

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒2 回

実験手順

1 g of 3-(2,6-difluorophenyl)-[1,2,4]triazin-6(1H)-one is placed in 20 ml of dioxane and at room temperature 0.73 g of POCl3 is added. Then, within a period of 5 min, 0.48 g of triethylamine in 3 ml of dioxane is added dropwise and stirring is carried out at room temperature for 30 min. The reaction mixture is then poured into ice-water and extracted with ethyl acetate, and the organic phase is separated off and concentrated. In this way 6-chloro-3-(2,6-difluorophenyl)-[1,2,4]triazine is obtained in the form of a yellow oil. The crude product is reacted further without purification.

後処理

  1. additionis added
  2. waitis carried out at room temperature for 30 min
  3. extractionextracted with ethyl acetate
  4. customthe organic phase is separated off
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-52dd45e26af841d19b4dd7ea3e589ce2
出典データセット
uspto-grants-2004_04
特許番号
US06723720B2

反応ノート

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