2-Amino-3-Hydroxypyridine → 2-(Chloromethyl)(1,3)oxazolo(4,5-b)pyridine

HRID 3923

反応式

HRID 3923 の反応式
[NH2:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][N:3]=1.[Cl:9][CH2:10][C:11](OCC)(OCC)OCC>COCCOCCOC>[Cl:9][CH2:10][C:11]1[O:8][C:7]2[C:2]([N:1]=1)=[N:3][CH:4]=[CH:5][CH:6]=2

参加物

4

実験手順

The commercially available 2-amino-3-hydroxypyridine (5.0 g) and diglyme (30 ml) were heated at 125° C. to obtain a solution. To this solution was added 2-chloro-1,1,1-triethoxyethane (9.9 g) and the mixture was held at 125° for 1 hour. The solution was cooled to room temperature and then decanted to remove a black byproduct residue. The filtrate was diluted with water (50 ml) and the resulting yellow precipitate was collected (1.5 g). A small sample was crystallized from isopropanol (m.p. 115°-118° C.).

後処理

  1. customto obtain a solution
  2. customdecanted
  3. customto remove a black byproduct residue
  4. additionThe filtrate was diluted with water (50 ml)
  5. customthe resulting yellow precipitate was collected (1.5 g)
  6. customA small sample was crystallized from isopropanol (m.p. 115°-118° C.)

出典と根拠

ORDレコード
ord-3b3a232422e4466d95c7b4b7201b4772
出典データセット
uspto-grants-1988_02
特許番号
US04723010

関連ノート

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