Cesium carbonate → 5-iodo-1-pyridin-3-yl-1H-indazole

HRID 1098896

反応式

HRID 1098896 の反応式
C(=O)([O-])[O-].[Cs+].[Cs+].F[C:8]1[CH:15]=[CH:14][C:13]([I:16])=[CH:12][C:9]=1[CH:10]=O.Cl.Cl.[N:19]1[CH:24]=[CH:23][CH:22]=[C:21]([NH:25][NH2:26])[CH:20]=1>CN1CCCC1=O>[I:16][C:13]1[CH:12]=[C:9]2[C:8](=[CH:15][CH:14]=1)[N:25]([C:21]1[CH:20]=[N:19][CH:24]=[CH:23][CH:22]=1)[N:26]=[CH:10]2

参加物

5

反応物 3

HCID 10796Cesium carbonateHCID 162170582-Fluoro-5-iodobenzaldehydeHCID 171324893-Hydrazinylpyridine dihydrochloride

生成物 1

HCID 597865715-iodo-1-pyridin-3-yl-1H-indazole収率 93.9%

試薬・触媒・溶媒 1

HCID 13387N-methyl-2-pyrrolidone溶媒

実験手順

Cesiumcarbonate (26.84 g, 82.38 mmol) is added to a suspension of 2-fluoro-5-iodobenzaldehyde (6.87 g, 27.46 mmol) and 3-pyridylhydrazine dihydrochloride (5 g, 27.46 mmol) in 136 mL N-methylpyrrolidon. The reaction mixture is stirred overnight at r.t. After checking that the hydrazone has been formed (1H-NMR) the reaction mixture is heated for 4 h at 160° C. The reaction mixture is allowed to cool down and the dark brown suspension is poured on 1000 mL ice water. After vigorously stirring at r.t. for 45 min, the precipitated product is sucked off via a glass microfibre filter, washed with water and dried at the evaporator at 45° C. 8.28 g (93.9%) of the title compound are obtained.

後処理

  1. customhas been formed (1H-NMR) the reaction mixture
  2. temperatureis heated for 4 h at 160° C
  3. temperatureto cool down
  4. stirringAfter vigorously stirring at r.t. for 45 min
  5. filtrationfilter
  6. washwashed with water
  7. customdried at the evaporator at 45° C

出典と根拠

ORDレコード
ord-19031bd0038e4074adb4246bc0b9ca97
出典データセット
uspto-grants-2012_03
特許番号
US08143290B2

関連ノート

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