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

HRID 218471
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HRID 218471 반응식
[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
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참가 물질

8

반응물 4

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

생성물 1

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

시약·촉매·용매 3

HCID 176Acetic Acid용매
HCID 1140
Toluene
용매
HCID 8857Ethyl Acetate용매

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-1d42f7f32eb244f9b0144d670273a255
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08198456B2

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