Ethylene Glycol → HCID 58516136、化合物
反応式
C([O:5][C:6](=[O:17])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:10]=1I)(C)(C)C.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:15][C:12]1[CH:13]=[CH:14][C:9]([O:8][CH2:7][C:6]([OH:5])=[O:17])=[C:10]([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:11]=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 (1) 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-8a9cf29b56d74c1a8a336d75cf50acce
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US08003703B2
反応ノート
読み込み中…