8-(Acetoxymethyl)-3-methylimidazo[1,2-a]pyridine → 2-[[(3-methylimidazo[1,2-a]pyridin-8-yl)methyl]thio]-1H-benzimidazole

HRID 1789207ノート

反応式

HRID 1789207 の反応式
C(O[CH2:5][C:6]1[C:7]2[N:8]([C:12]([CH3:15])=[CH:13][N:14]=2)[CH:9]=[CH:10][CH:11]=1)(=O)C.[SH:16][C:17]1[NH:18][C:19]2[CH:25]=[CH:24][CH:23]=[CH:22][C:20]=2[N:21]=1>Br.C(O)(=O)C>[CH3:15][C:12]1[N:8]2[CH:9]=[CH:10][CH:11]=[C:6]([CH2:5][S:16][C:17]3[NH:21][C:20]4[CH:22]=[CH:23][CH:24]=[CH:25][C:19]=4[N:18]=3)[C:7]2=[N:14][CH:13]=1

参加物

5

反応物 2

HCID 201888528-(Acetoxymethyl)-3-methylimidazo[1,2-a]pyridineHCID 178527775HCID 178527775、化合物

生成物 1

HCID 201888372-[[(3-methylimidazo[1,2-a]pyridin-8-yl)methyl]thio]-1H-benzimidazole収率 64.9%

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 260Hydrogen Bromide溶媒

実験手順

A mixture of 5.0 g (30 mmole) of 3-(acetoxymethyl)-2-pyridinamine and 4.8 g (35 mmole) of 2-bromopropanal spontaneously heated upon mixing. After cooling, the mixture was partitioned between aqueous potassium carbonate and dichloromethane. The organic phase was separated, washed with water, dried over magnesium sulfate, filtered, and concentrated in vacuo. Chromatography on silica gel (using ethanol-dichloromethane as eluent) yielded 2.3 g of 8-(acetoxymethyl)-3-methylimidazo[1,2-a]pyridine, as confirmed by the nmr and infrared spectra and by elemental analysis. [Calcd. for C11H12N2O2 : C, 64.69; H, 5.92; N, 13.72. Found: C, 63.70; H, 5.85; N, 14.24). A mixture of 2.3 g (11 mmole) of 8-(acetoxymethyl)-3-methylimidazo[1,2-a]pyridine and 1.65 g (11 mmole) of 2-mercaptobenzimidazole in 40 ml of 15% hydrogen bromide in acetic acid was heated on a steam bath. After being cooled to room temperature, the mixture was partitioned between 5% aqueous sodium hydroxide and dichloromethane. The organic layer was dried over sodium sulfate, filtered, and concentrated to an oil. Chromatography yielded 2.1 g of the title compound. Structure assignment was supported by the nmr and infrared spectra.

後処理

  1. temperaturewas heated on a steam bath
  2. customthe mixture was partitioned between 5% aqueous sodium hydroxide and dichloromethane
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated to an oil

出典と根拠

ORDレコード
ord-53c734d52032499ab6a88264f406cab5
出典データセット
uspto-grants-1987_08
特許番号
US04687775

反応ノート

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