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5-(hydroxy methyl)-2-propyl-4-(2,5-dimethyl-1H-pyrrol-1-yl)imidazole → 4-(2,5-dimethyl-1H-pyrrol 1-yl)-2-propylimidazole-5-carboxaldehyde

HRID 248640
ノート
印刷プレビュー

反応式

HRID 248640 の反応式
[OH:1][CH2:2][C:3]1[NH:7][C:6]([CH2:8][CH2:9][CH3:10])=[N:5][C:4]=1[N:11]1[C:15]([CH3:16])=[CH:14][CH:13]=[C:12]1[CH3:17]>C1COCC1.O=[Mn]=O>[CH3:17][C:12]1[N:11]([C:4]2[N:5]=[C:6]([CH2:8][CH2:9][CH3:10])[NH:7][C:3]=2[CH:2]=[O:1])[C:15]([CH3:16])=[CH:14][CH:13]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 149628935-(hydroxy methyl)-2-propyl-4-(2,5-dimethyl-1H-pyrrol-1-yl)imidazole

生成物 1

HCID 149628924-(2,5-dimethyl-1H-pyrrol 1-yl)-2-propylimidazole-5-carboxaldehyde収率 75%

試薬・触媒・溶媒 2

HCID 14801Manganese dioxide触媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 5-(hydroxy-methyl)-2-propyl-4-(2,5-dimethyl-1H-pyrrol-1-yl)imidazole (Example 48, 6.0 g, 0.026 mol) in dry THF (125 mL) was added MnO2 (11.2 g, 0.13 mol) and the reaction mixture refluxed for 4 hours under an atmosphere of nitrogen. The reaction mixture was cooled, filtered through celite, and the resulting filtrate evaporated under reduced pressure. Purification by flash chromatography (silica; 2:1 hexane ethyl acetate) gave the title compound 4-(2,5-dimethyl-1H-pyrrol 1-yl)-2-propylimidazole-5-carboxaldehyde (4.5 g, 75%), mp 119°-121° C.

後処理

  1. temperaturethe reaction mixture refluxed for 4 hours under an atmosphere of nitrogen
  2. temperatureThe reaction mixture was cooled
  3. filtrationfiltered through celite
  4. customthe resulting filtrate evaporated under reduced pressure
  5. customPurification by flash chromatography (silica; 2:1 hexane ethyl acetate)

出典と根拠

ORDレコード
ord-f7400e04e5fa4143bf49ca81293e0c03
出典データセット
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05210211

反応ノート

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