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Dimethyl Sulfoxide → 6-Chloro-1-(tetrahydro-pyran-2-yl)-1H-indazole-3-carbaldehyde

HRID 1827460
ノート
印刷プレビュー

反応式

HRID 1827460 の反応式
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH2:17][OH:18])=[N:7][N:8]2[CH:11]2[CH2:16][CH2:15][CH2:14][CH2:13][O:12]2)=[CH:4][CH:3]=1.CS(C)=O>CCOC(C)=O.O>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH:17]=[O:18])=[N:7][N:8]2[CH:11]2[CH2:16][CH2:15][CH2:14][CH2:13][O:12]2)=[CH:4][CH: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 2

HCID 679Dimethyl SulfoxideHCID 22136538[6-Chloro-1-(tetrahydro-pyran-2-yl)-1H-indazol-3-yl]-methanol

生成物 1

HCID 221365606-Chloro-1-(tetrahydro-pyran-2-yl)-1H-indazole-3-carbaldehyde収率 98%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8857Ethyl Acetate溶媒

実験手順

A solution of [6-Chloro-1-(tetrahydro-pyran-2-yl)-1H-indazol-3-yl]-methanol (1.75 g, 6.58 mmol), IBX (2.76 g, 9.87 mmol) and DMSO (27 mL) was stirred overnight. The reaction was diluted in EtOAc and water. The layers were separated, and the aqueous was extracted with EtOAc (3×100 mL). The organics were combined and washed with saturated NaCl (100 mL). The organic was dried over MgSO4, filtered, and then concentrated to a solid. The solid was dissolved in CH2Cl2, and filtered. The organic was evaporated to yield the desired product (1.707 g, 92%).

後処理

  1. customThe layers were separated
  2. extractionthe aqueous was extracted with EtOAc (3×100 mL)
  3. washwashed with saturated NaCl (100 mL)
  4. dry with materialThe organic was dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated to a solid
  7. dissolutionThe solid was dissolved in CH2Cl2
  8. filtrationfiltered
  9. customThe organic was evaporated

出典と根拠

ORDレコード
ord-351d824f6538412aa306223e03e08d50
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07053107B2

反応ノート

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