Dimethyl Sulfoxide → 5-Pentylbenzimidazol-2-one

HRID 2233544

反応式

HRID 2233544 の反応式
[CH3:1][C:2]1[CH:11]=[CH:10][C:5]2=[N:6][C:7](=[O:9])[N:8]=[C:4]2[CH:3]=1.[O-]CC.[Na+].CS(C)=O.Br[CH2:21][CH2:22][CH2:23][CH3:24]>C(O)C>[CH2:1]([C:2]1[CH:11]=[CH:10][C:5]2=[N:6][C:7](=[O:9])[N:8]=[C:4]2[CH:3]=1)[CH2:21][CH2:22][CH2:23][CH3:24]

参加物

6

実験手順

To a solution of 5-methylbenzimidazol-2-one (50 mg, 3.378×10−4 mol) in dry ethanol (5 ml), the freshly made sodium ethoxide in ethanol (1M, 1.01×10−3 mol equivalents) was added dropwise under a nitrogen atmosphere. At room temperature the mixture was stirred for 3 hrs under an atmosphere of nitrogen and the ethanol was then removed under reduced pressure. To this a solution of dry DMSO (3 ml) and 1-bromobutane (54 μl, 5.1×10−4 mol) was added and stirred at room temperature under an atmosphere of nitrogen overnight. The reaction mixture was then quenched with ice and neutralised using 1M hydrochloric acid solution, forming a white solid product. The solid was collected by filtration and purified using preparative thin liquid chromatography with 10% MeOH/CHCl3.

後処理

  1. customthe ethanol was then removed under reduced pressure
  2. stirringstirred at room temperature under an atmosphere of nitrogen overnight
  3. customThe reaction mixture was then quenched with ice
  4. customforming a white solid product
  5. filtrationThe solid was collected by filtration
  6. custompurified

出典と根拠

ORDレコード
ord-54938d4a31ba44f994559747aa8c38a1
出典データセット
uspto-grants-2010_05
特許番号
US07709514B2

関連ノート

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