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Potassium Carbonate → 4-((2,6-Dichloro-9h-purin-9-yl)methyl)benzonitrile

HRID 2170068
ノート
印刷プレビュー

反応式

HRID 2170068 の反応式
[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][NH:8]2)=[C:4]([Cl:11])[N:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]#[N:27])=[CH:22][CH:21]=1>CN(C=O)C>[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH2:19][C:20]2[CH:25]=[CH:24][C:23]([C:26]#[N:27])=[CH:22][CH:21]=2)=[C:4]([Cl:11])[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

5

反応物 3

HCID 11430Potassium CarbonateHCID 869964-(Bromomethyl)benzonitrileHCID 178418875CID 79540

生成物 1

HCID 141986094-((2,6-Dichloro-9h-purin-9-yl)methyl)benzonitrile

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

2,6-dichloro-9H-purine (16 mmol) is dissolved in DMF (50 mL) and potassium carbonate (50 mmol) is added. α-Bromo-p-tolunitrile (22 mmol) is then added and the mixture is stirred at ambient temperature for 16 hours. After filtration to remove insoluble inorganic salts, the filtrate is poured into water (1500 mL) and extracted with ethyl acetate (2×400 mL), dried over magnesium sulfate and evaporated to yield a residue which is subjected to flash silica gel chromatography using 1:2:10 ethyl acetate/acetone/hexanes. Yield 3.33 g (69%). UV, NMR and MS were consistent with structure assignment.

後処理

  1. filtrationAfter filtration
  2. customto remove insoluble inorganic salts
  3. additionthe filtrate is poured into water (1500 mL)
  4. extractionextracted with ethyl acetate (2×400 mL)
  5. dry with materialdried over magnesium sulfate
  6. customevaporated
  7. customto yield a residue which

出典と根拠

ORDレコード
ord-b21414109b8c40898b0e474c05aec652
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09050376B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート