反応式
[CH3:1][N:2]([CH2:4][C:5]([NH:7][NH2:8])=O)[CH3:3].Cl.C([O-])([O-])=O.[Cs+].[Cs+].[CH3:16][N:17]=[C:18]=[S:19]>CCO>[CH3:1][N:2]([CH2:4][C:5]1[N:17]([CH3:16])[C:18]([SH:19])=[N:8][N:7]=1)[CH3:3]参加物
実験手順
N,N-dimethylglycine hydrazide hydrochloride (50 g, 0.263 mol) was stirred for 5 min in EtOH (525 mL). To this suspension was added Cs2CO3 (62.5 g, 0.192 mol) and the mixture was stirred at room temperature for 15 min. Methyl isothiocyanate (19.25 g, 0.263 mol) in EtOH (270 mL) was added to the pot and the reaction mixture was brought to reflux. The reflux condenser was removed and the EtOH was allowed to evaporate under atmospheric pressure (oil bath temperature 105–110° C.) over 3 h to give a purple paste. The reaction was removed from heat and allowed to sit at room temperature overnight (18 h), during which time the paste became a solid. The solid was mixed with CH2Cl2 (1.5 L) and filtered. The organic filtrate was concentrated under reduced pressure to give 31 g of a crude yellow oil. The oil was purified by column chromatography through silica gel, eluting with 4:1 CH2Cl2/MeOH to afford 15.3 g (34.9%) of the desired product.
後処理
- temperatureto reflux
- customThe reflux condenser was removed
- customto evaporate under atmospheric pressure (oil bath temperature 105–110° C.) over 3 h
- customto give a purple paste
- customThe reaction was removed
- temperaturefrom heat
- waitto sit at room temperature overnight
- custom(18 h)
- additionThe solid was mixed with CH2Cl2 (1.5 L)
- filtrationfiltered
- concentrationThe organic filtrate was concentrated under reduced pressure
- customto give 31 g of a crude yellow oil
- customThe oil was purified by column chromatography through silica gel
- washeluting with 4:1 CH2Cl2/MeOH
出典と根拠
- ORDレコード
- ord-31ecad0905d1462eac13c90fffd1b8d5
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- US07148226B2
関連ノート
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