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Isoamyl Nitrite → 5-Iodo-1H-pyrazolo[3,4-c]pyridine

HRID 218471
ノート
印刷プレビュー

反応式

HRID 218471 の反応式
[I:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([NH2:9])=[CH:4][N:3]=1.CC([O-])=O.[K+].[N:15](OCCC(C)C)=O.C([O-])(O)=O.[Na+]>C1(C)C=CC=CC=1.CCOC(C)=O.CC(O)=O>[I:1][C:2]1[CH:7]=[C:6]2[CH:8]=[N:15][NH:9][C:5]2=[CH:4][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

8

反応物 4

HCID 8053Isoamyl NitriteHCID 516892Sodium BicarbonateHCID 517044Potassium AcetateHCID 230701206-Iodo-4-methylpyridin-3-amine

生成物 1

HCID 597632735-Iodo-1H-pyrazolo[3,4-c]pyridine収率 83.5%

試薬・触媒・溶媒 3

HCID 176Acetic Acid溶媒
HCID 1140
Toluene
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To a suspension of 2-iodo-4-methyl-5-pyridinamine (5 g, 21.4 mmol) in toluene (340 mL) was added HOAc (19 mL), and the mixture was stirred vigorously until it became clear. Then KOAc (15.78 g, 160.23 mmol) was added. To this white suspension, isoamyl nitrite (3.16 mL, 23.5 mmol) was added dropwise at rt, and the resulting mixture was stirred for 2 days. The reaction mixture was diluted with EtOAc and treated with NaHCO3 (sat.) to pH 10. The reaction mixture was extracted with EtOAc, washed with brine, dried, and concentrated in vacuo to afford the crude product. Purification by flash chromatography afforded 5-iodo-1H-pyrazolo[3,4-c]pyridine (4.37 g, 83.5%).

後処理

  1. stirringthe resulting mixture was stirred for 2 days
  2. extractionThe reaction mixture was extracted with EtOAc
  3. washwashed with brine
  4. customdried
  5. concentrationconcentrated in vacuo
  6. customto afford the crude product
  7. customPurification by flash chromatography

出典と根拠

ORDレコード
ord-1d42f7f32eb244f9b0144d670273a255
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08198456B2

反応ノート

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