Ethylene Glycol → HCID 58516136、化合物
反応式
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][CH2:7][C:8]([O:10]C(C)(C)C)=[O:9])=[C:4](I)[CH:3]=1.Cl.[N:19]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][C:27]=2[SH:29])[CH:22]=[CH:21][CH:20]=1.C(=O)([O-])[O-].[K+].[K+].C(O)CO>C(O)(C)C.[Cu]I>[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][CH2:7][C:8]([OH:10])=[O:9])=[C:4]([S:29][C:27]2[CH:26]=[CH:25][CH:24]=[C:23]3[C:28]=2[N:19]=[CH:20][CH:21]=[CH:22]3)[CH:3]=1参加物
7
反応条件
- 温度
- 80 °C
実験手順
A mixture of the product from step (i) (0.262 g), 8-quinolinethiol hydrochloride (0.141 g), copper (I) iodide (7 mg), potassium carbonate (0.295 g) and ethylene glycol (0.08 ml) in iso-propanol (3 ml) was heated at 80° C. for 48 h. The mixture was partitioned between DCM/2M hydrochloric acid, the organics dried, evaporated under reduced pressure and the residue purified by chromatography on silica eluting with DCM:methanol:acetic acid (90:9:1). The residue was triturated with diethylether/methanol, filtered and dried, yield 0.101 g.
後処理
- customThe mixture was partitioned between DCM/2M hydrochloric acid
- customthe organics dried, evaporated under reduced pressure
- customthe residue purified by chromatography on silica eluting with DCM:methanol:acetic acid (90:9:1)
- customThe residue was triturated with diethylether/methanol
- filtrationfiltered
- customdried
出典と根拠
- ORDレコード
- ord-21d41ea1545a4be8a7f845b5b6e4f36d
- 出典データセット
- uspto-grants-2013_03
- 特許番号
- US08394986B2
反応ノート
読み込み中…