反応式
I[C:2]1[S:3][CH:4]=[CH:5][CH:6]=1.[C:7]([O:11][C:12]([N:14]1[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]1)=[O:13])([CH3:10])([CH3:9])[CH3:8].C(O)CO.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>[Cu]I.C(OCC)(=O)C.CC(O)C>[C:7]([O:11][C:12]([N:14]1[CH2:19][CH2:18][N:17]([C:2]2[S:3][CH:4]=[CH:5][CH:6]=2)[CH2:16][CH2:15]1)=[O:13])([CH3:10])([CH3:8])[CH3:9]参加物
8
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
A mixture of 2-iodothiophene (Aldrich Co., 1.0 g), 1-(tert-butoxycarbonyl)piperazine (Aldrich Co. (hereafter the same), 1.06 g), copper(I) iodide (45 mg), ethylene glycol (530 μl), potassium phosphate (2.02 g) and 2-propanol (5 ml) was heated under reflux for 20 hr. Ethyl acetate was added, and the mixture was filtered through a Celite (trademark) filter. The filtrate was washed 3 times with 28% aqueous ammonia, and then washed with saturated brine. The solvent was evaporated under reduced pressure to give a brown solid. The solid was purified by silica gel column chromatography (elution solvent: ethyl acetate-hexane (7:3)) to give 4-(2-thienyl)piperazine-1-carboxylic acid tert-butyl ester (984 mg, yield 77%).
後処理
- temperatureunder reflux for 20 hr
- filtrationthe mixture was filtered through a Celite (trademark)
- filtrationfilter
- washThe filtrate was washed 3 times with 28% aqueous ammonia
- washwashed with saturated brine
- customThe solvent was evaporated under reduced pressure
- customto give a brown solid
- customThe solid was purified by silica gel column chromatography (elution solvent: ethyl acetate-hexane (7:3))
出典と根拠
- ORDレコード
- ord-ffc748b1030f4f6abf2f239762f169db
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US07994196B2
関連ノート
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