1,2-Dichloroethane → HCID 57180353、化合物
反応式
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH2:28][CH:29]1[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1)[C@@H:10]([O:19][Si:20](OC(C)(C)C)([CH3:22])[CH3:21])[CH2:11][NH:12][CH2:13][CH2:14][CH2:15][C:16](O)=[O:17])=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:35](Cl)CCl.C1C=C[C:42]2N(O)N=N[C:43]=2[CH:44]=1.O>C(Cl)Cl>[O:19]([C@@H:10]([CH2:11][N:12]1[CH2:13][CH2:14][CH2:15][C:16]1=[O:17])[C@@H:9]([NH:8][C:6](=[O:7])[O:5][C:1]([CH3:3])([CH3:2])[CH3:4])[CH2:28][CH:29]1[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1)[Si:20]([C:43]([CH3:42])([CH3:44])[CH3:35])([CH3:22])[CH3:21]参加物
実験手順
0.6 g (1.23 mmol) of 4-[[(2S,3S)-3-(1-t-butoxyformamido)-2-(t-butoxydimethylsiloxy)-3-(cyclohexylmethyl)propyl]amino]butyric acid was dissolved in 2 ml of methylene chloride and added dropwise at -20° to a solution of 285 mg of EDC and 200 mg of HOBT in 13 ml of methylene chloride. The reaction mixture was subsequently warmed to room temperature within 15 minutes, stirred at this temperature for 17 hours and subsequently poured into water and extracted with methylene chloride. The methylene chloride extracts were dried over magnesium sulfate, evaporated under reduced pressure and the residue was chromatographed on 10 g of silica gel using a mixture of methylene chloride and isopropanol as the eluting agent, whereby there were obtained 480 mg of t-butyl [(1S,2S)-2-(t-butyldimethylsiloxy)-1-(cyclohexylmethyl)-3-(2-oxo-1-pyrrolidinyl)propyl]carbamate as an oil which was used directly in the next step.
後処理
- extractionextracted with methylene chloride
- dry with materialThe methylene chloride extracts were dried over magnesium sulfate
- customevaporated under reduced pressure
- customthe residue was chromatographed on 10 g of silica gel using
- additiona mixture of methylene chloride and isopropanol as the eluting agent
出典と根拠
- ORDレコード
- ord-38a8554eaa964671aff82ef1c240324a
- 出典データセット
- uspto-grants-1994_01
- 特許番号
- US05278148
反応ノート
読み込み中…