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Water → 5-Fluoro-1-[(3-fluoropyridin-2-yl)methyl]-3-iodo-1H-pyrazolo[3,4-b]pyridine

HRID 536483
ノート
印刷プレビュー

反応式

HRID 536483 の反応式
[F:1][C:2]1[CH:3]=[C:4]2[C:10]([I:11])=[N:9][NH:8][C:5]2=[N:6][CH:7]=1.C(=O)([O-])[O-].[Cs+].[Cs+].Br[CH2:19][C:20]1[C:25]([F:26])=[CH:24][CH:23]=[CH:22][N:21]=1.O>CN(C=O)C>[F:1][C:2]1[CH:3]=[C:4]2[C:10]([I:11])=[N:9][N:8]([CH2:19][C:20]3[C:25]([F:26])=[CH:24][CH:23]=[CH:22][N:21]=3)[C:5]2=[N:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 10796Cesium carbonateHCID 216131732-(Bromomethyl)-3-fluoropyridineHCID 178505979HCID 178505979、化合物

生成物 1

HCID 711874705-Fluoro-1-[(3-fluoropyridin-2-yl)methyl]-3-iodo-1H-pyrazolo[3,4-b]pyridine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒
2 回

実験手順

6.291 g (23.921 mmol) of 5-fluoro-3-iodo-1H-pyrazolo[3,4-b]pyridine and 8.573 g (26.313 mmol) of caesium carbonate were put in DMF (10 ml) and then 5.00 g (26.313 mmol) of 2-(bromomethyl)-3-fluoropyridine dissolved in DMF (20 ml) was added dropwise. The mixture was stirred overnight at RT. Then it was left to cool and was poured into 200 ml water. A precipitate was filtered off with suction, it was washed with water and dried overnight under high vacuum. 6.28 g (70% of theor.) of the title compound was obtained.

後処理

  1. additionwas added dropwise
  2. waitThen it was left
  3. temperatureto cool
  4. filtrationA precipitate was filtered off with suction, it
  5. washwas washed with water
  6. customdried overnight under high vacuum

出典と根拠

ORDレコード
ord-80279174063a4dc68f48bdf233535389
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08859569B2

反応ノート

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