反応式
[NH:1](C(OC(C)(C)C)=O)[C@@H:2]([C:30]([NH:32][CH2:33][C:34]([NH:36][C@H:37]([C:55]([OH:57])=[O:56])[CH2:38][CH2:39][CH2:40][NH:41][C:42](=[NH:54])[NH:43]S(C1C=CC(C)=CC=1)(=O)=O)=[O:35])=[O:31])[CH2:3][CH2:4][CH2:5][NH:6][C:7](=[NH:29])[N:8](C(OCC1C=CC=CC=1)=O)C(OCC1C=CC=CC=1)=O.[S:65]1[CH:69]=[CH:68][N:67]=[CH:66]1.C1(OC)C=CC=CC=1.N#N>CSCC.CCOCC.CCCCCC>[NH2:1][C@@H:2]([C:30]([NH:32][CH2:33][C:34]([NH:36][C@H:37]([C:55]([OH:57])=[O:56])[CH2:38][CH2:39][CH2:40][NH:41][C:42](=[NH:43])[NH2:54])=[O:35])=[O:31])[CH2:3][CH2:4][CH2:5][NH:6][C:7](=[NH:8])[NH2:29].[S:65]1[CH:69]=[CH:68][N:67]=[CH:66]1参加物
6
反応条件
- 温度
- 0 °C
実験手順
A 100 mg portion of Boc-(D)-Arg(Cbz2)-Gly-Arg(Tos)-Thiazole, 1 mL of anisole and 4 drops of MeSEt were placed in HF-cleavage vessel and cooled under liquid N2. HF (10 mL) was then condensed into the reaction mixture and stirred at 0° C. for 1.25 h. HF was removed under vacuum to give a gum-like residue which was titrated with 20 mL of 50% Et2O-hexane and the organic wash removed by filtration. The gum residue was dissolved in 30 mL of 30% aq. HOAc and filtered through the above sintered funnel. The filtrate was lyophilized to give a powder which was purified by RP-HPLC to give 28 mg (60% yield) of (D)-Arg-Gly-Arg-thiazole. FAB-MS (M+H)+ =455.2
後処理
- customcondensed into the reaction mixture
- customHF was removed under vacuum
- customto give a gum-like residue which
- washthe organic wash
- customremoved by filtration
- dissolutionThe gum residue was dissolved in 30 mL of 30% aq. HOAc
- filtrationfiltered through the above sintered funnel
- customto give a powder which
- customwas purified by RP-HPLC
出典と根拠
- ORDレコード
- ord-283db2cfbe884f068a53863e057d09e1
- 出典データセット
- uspto-grants-2000_05
- 特許番号
- US06069130
関連ノート
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