1,2-Dichloroethane → HCID 57180353, 화합물
반응식
[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]참가 물질
실험 절차
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.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-38a8554eaa964671aff82ef1c240324a
- 출처 데이터셋
- uspto-grants-1994_01
- 특허 번호
- US05278148
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