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Tetrafluoroboric acid → HCID 178481919、化合物

HRID 72703
ノート
印刷プレビュー

反応式

HRID 72703 の反応式
[CH3:1][N:2]1[C:6]2=[N:7][CH:8]=[N:9][C:10]([OH:11])=[C:5]2[CH:4]=[N:3]1.[I:12]N1C(=O)CCC1=O.F[B-](F)(F)F.[H+].C(=O)(O)[O-].[Na+]>C(#N)C.O>[I:12][C:4]1[C:5]2[C:6](=[N:7][CH:8]=[N:9][C:10]=2[OH:11])[N:2]([CH3:1])[N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 28118Tetrafluoroboric acidHCID 120273N-IodosuccinimideHCID 516892Sodium BicarbonateHCID 178481767HCID 178481767、化合物

生成物 1

HCID 178481919HCID 178481919、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6342
Acetonitrile
溶媒

実験手順

1-Methyl-1H-pyrazolo[3,4-d]pyrimidin-4-ol (5.50 g, 36.6 mmol) was combined with N-iodosuccinimide (97%, 12.7 g, 54.8 mmol) and tetrafluoroboric acid (50% solution in water, 23.0 mL, 183 mmol) in acetonitrile (50 mL) and the reaction mixture was heated to reflux for 5 hours. After cooling to room temperature, the reaction mixture was poured portion-wise into water (50 mL) containing sodium bicarbonate (18.6 g, 220 mmol). When gas evolution had ceased, the mixture was filtered, and the dark solid was washed successively with saturated aqueous sodium thiosulfate solution (25 mL) and water (2×25 mL). The resulting solid was dried under vacuum overnight at 50° C. to afford the product as a cream-colored solid. Yield: 9.35 g, 33.9 mmol, 93%. LCMS m/z 277.0 (M+1). 1H NMR (500 MHz, DMSO-d6) δ 3.87 (s, 3H), 8.07 (s, 1H), 12.08 (v br s, 1H).

後処理

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux for 5 hours
  3. filtrationthe mixture was filtered
  4. washthe dark solid was washed successively with saturated aqueous sodium thiosulfate solution (25 mL) and water (2×25 mL)
  5. customThe resulting solid was dried under vacuum overnight at 50° C.

出典と根拠

ORDレコード
ord-66b0366bb8ec4ba5989d196a35c4a5eb
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08829010B2

反応ノート

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