2-Pyridinamine, 5-iodo- → 5-Phenoxypyridin-2-amine
反応式
[C:1]1([O-:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[K+].[NH2:9][C:10]1[CH:15]=[CH:14][C:13](I)=[CH:12][N:11]=1>CC(N(C)C)=O>[NH2:9][C:10]1[CH:15]=[CH:14][C:13]([O:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[CH:12][N:11]=1参加物
4
実験手順
3.3 G. of potassium phenolate, 5.47 g. of 2-amino 5-iodopyridine and 1.78 g. of cuprous oxide in 150 ml. of dimethylacetamide are heated at reflux under a nitrogen atmosphere for 24 hours. The solvent is removed in vacuo and the residue is extracted with chloroform. Chromatography of the methylene chloride soluble portion with silica gel and elution with ethyl acetate yields 2-amino-5-phenoxy pyridine m.p. 67°-69° C.
後処理
- temperatureat reflux under a nitrogen atmosphere for 24 hours
- customThe solvent is removed in vacuo
- extractionthe residue is extracted with chloroform
- washChromatography of the methylene chloride soluble portion with silica gel and elution with ethyl acetate
出典と根拠
- ORDレコード
- ord-eaa44ef71d95469786d79e2ca79f7d0d
- 出典データセット
- uspto-grants-1978_06
- 特許番号
- US04096264
反応ノート
読み込み中…