反応式
[C:1]([C:9]1[CH:10]=[C:11]([CH:18]=[CH:19][CH:20]=1)[CH2:12][C@@H:13]([C:15]([OH:17])=[O:16])[NH2:14])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[CH3:28][C:29]([O:32][C:33](ON=C(C1C=CC=CC=1)C#N)=[O:34])([CH3:31])[CH3:30]>O.CC(C)=O>[C:33]([NH:14][C@H:13]([C:15]([OH:17])=[O:16])[CH2:12][C:11]1[CH:18]=[CH:19][CH:20]=[C:9]([C:1](=[O:8])[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:10]=1)([O:32][C:29]([CH3:31])([CH3:30])[CH3:28])=[O:34]参加物
実験手順
A suspension of 2.175 g of m-benzoyl-L-phenylalanine in 25 ml of water and 1.15 g of triethylamine was treated with 3.35 g of BOC-ON in 40 ml of acetone. After 3 h, acetone was removed and the aqueous residue was extracted three times with ether (discarded). The aqueous solution was acidified to pH 2 with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried (MgSO4) and stripped. The residue was triturated for 7 days with petroleum ether. The waxy insoluble solid was triturated for 14 days with an additional portion of petroleum ether and finally for 7 days with a third portion. The resulting white solid weighed 1.786 g after vacuum drying, [α]D25 +22.2±0.9°, C=0.86 g/100 ml ethanol. Anal.: Calcd. for C21H23NO5 :C, 68.28; H, 6.28; N, 3.79. Found: C, 68.01; H, 6.49; N, 3.68.
後処理
- customacetone was removed
- extractionthe aqueous residue was extracted three times with ether (discarded)
- extractionextracted with ethyl acetate
- dry with materialThe extract was dried (MgSO4)
- customThe residue was triturated for 7 days with petroleum ether
- customThe waxy insoluble solid was triturated for 14 days with an additional portion of petroleum ether and finally for 7 days with a third portion
- customdrying
出典と根拠
- ORDレコード
- ord-0315a666c64b43fd98a8efb3ebeb32e5
- 出典データセット
- uspto-grants-1988_08
- 特許番号
- US04762881
関連ノート
読み込み中…