1-Bromo-3-chloropropane → 5-(3-Chloro-propoxy)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic Acid Ethyl Ester
反応式
[CH3:1][CH2:2][O:3][C:4]([C:6]1[N:15](C(OC(C)(C)C)=O)[C:9]2=[N:10][CH:11]=[C:12]([OH:14])[CH:13]=[C:8]2[CH:7]=1)=[O:5].C(=O)([O-])[O-].[K+].[K+].Br[CH2:30][CH2:31][CH2:32][Cl:33].[Cl-].[NH4+]>CC(=O)CC>[CH2:2]([O:3][C:4]([C:6]1[NH:15][C:9]2=[N:10][CH:11]=[C:12]([O:14][CH2:30][CH2:31][CH2:32][Cl:33])[CH:13]=[C:8]2[CH:7]=1)=[O:5])[CH3:1]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
The suspension consistent of 0.5 g (2.4 mmol) 5-hydroxy-pyrrolo[2,3-b]pyridine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (as prepared in WO 05/000849), 0.4 g (2.6 mmol) potassium carbonate and 0.29 ml (0.46 g, 2.9 mmol) 1-bromo-3-chloropropane in 10 ml 2-butanone was heated under reflux for 23 hours. The reaction mixture was poured on 10% aqueous ammonium chloride solution and was extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was flash-chromatographed on silica gel with n-heptane:ethyl acetate (1:1 v/v) as eluant to give 0.22 g (32%) of the desired compound as a colorless solid.
後処理
- temperatureunder reflux for 23 hours
- extractionwas extracted three times with ethyl acetate
- washThe combined organic layers were washed with brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated
- customThe residue was flash-chromatographed on silica gel with n-heptane:ethyl acetate (1:1 v/v) as eluant
出典と根拠
- ORDレコード
- ord-46a7a713c3f94c5a9ece1db084dd7095
- 出典データセット
- uspto-grants-2009_11
- 特許番号
- US07622466B2
反応ノート
読み込み中…