반응식
[C:1]([NH:11][C@H:12]([C:18]([OH:20])=[O:19])[CH2:13][CH2:14][CH2:15][CH2:16][NH2:17])([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].C(O[C:25]([CH3:28])([CH3:27])[CH3:26])(=O)C.Cl(O)(=O)(=O)=O.[OH-].[Na+]>O.C(OCC)(=O)C>[C:1]([NH:11][C@H:12]([C:18]([O:20][C:25]([CH3:28])([CH3:27])[CH3:26])=[O:19])[CH2:13][CH2:14][CH2:15][CH2:16][NH2:17])([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2]참가 물질
실험 절차
A mixture of 25 g of Nα-CBZ-L-lysine from Sigma, where CBZ is benzyloxycarbonyl, 250 mL of t-butyl acetate and 14 mL of 70% perchloric acid was vigorously mixed until all solids were dissolved. After stirring overnight, 375 mL of ethyl acetate was added followed by 250 mL of water. The pH of the aqueous layer was raised to 5.5 with 20% NaOH whereupon the organic phase was separated. The aqueous phase was extracted with the ethyl acetate solution and the pH again raised to 10.5 whereupon it was again extracted with 200 mL of fresh ethyl acetate. The organic extracts were combined, washed with saturated brine, dried over Na2SO4 and concentrated. The residue was dried overnight under high vacuum to yield 23.2 g of a colorless, viscous material.
후처리
- additionwas vigorously mixed until all solids
- dissolutionwere dissolved
- customwas separated
- extractionThe aqueous phase was extracted with the ethyl acetate solution
- temperaturethe pH again raised to 10.5 whereupon it
- extractionwas again extracted with 200 mL of fresh ethyl acetate
- washwashed with saturated brine
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customThe residue was dried overnight under high vacuum
- customto yield 23.2 g of a colorless, viscous material
출처 및 근거
- ORD 기록
- ord-138236e224a34c72b9402d81270c32cc
- 출처 데이터셋
- uspto-grants-1998_03
- 특허 번호
- US05723619
연결된 노트
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