Dichloromethane → (trans)-1-[[(3-Ethoxy-3-oxopropyl)ethylamino]carbonyl]-4-hydroxy-L-proline, phenylmethyl ester
反応式
ClCCl.Cl.[OH:5][C@H:6]1[CH2:10][NH:9][C@H:8]([C:11]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[O:12])[CH2:7]1.[CH3:21][N:22]1[CH2:27][CH2:26]O[CH2:24][CH2:23]1.OC1CN[C@H]([C:34]([O:36][CH2:37][C:38]2C=CC=CC=2)=[O:35])C1.C(OCC)(=[O:46])C>>[CH2:37]([O:36][C:34](=[O:35])[CH2:26][CH2:27][N:22]([CH2:23][CH3:24])[C:21]([N:9]1[CH2:10][C@H:6]([OH:5])[CH2:7][C@H:8]1[C:11]([O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:12])=[O:46])[CH3:38]参加物
反応物 5
生成物 1
実験手順
This residue is dissolved in 30 ml. of dichloromethane and (trans)-4-hydroxy-L-proline, phenylmethyl ester, hydrochloride (6.9 g., 1.2 eq.) is added. To the resulting suspension is added dropwise N-methylmorpholine (5.6 ml., 2.4 eq.) in 20 ml. of dichloromethane. The resulting mixture is stirred at room temperature for 15 hours. The solvent is removed at reduced pressure and the residue taken up in ethyl acetate. This is washed with water (twice), 1N hydrochloric acid (twice), 1N sodium bicarbonate (twice), and once with brine. After drying (MgSO4), the solvent is removed at reduced pressure. The residue is flash chromatographed (Whatman silica gel LPS-1, hexane:ethyl acetate; 65:35) to give 7.72 g. of (trans)-1-[[3-ethoxy-3-oxopropyl)ethylamino]carbonyl]-4-hydroxy-L-proline, phenylmethyl ester as a colorless oil; TLC (silica gel, ethyl acetate) Rf =0.34.
後処理
- dissolutionThis residue is dissolved in 30 ml
- customThe solvent is removed at reduced pressure
- washThis is washed with water (twice), 1N hydrochloric acid (twice), 1N sodium bicarbonate (twice), and once with brine
- dry with materialAfter drying (MgSO4)
- customthe solvent is removed at reduced pressure
- customchromatographed (Whatman silica gel LPS-1, hexane:ethyl acetate; 65:35)
- customto give 7.72 g
出典と根拠
- ORDレコード
- ord-207a0729442548fcb09265955604ecc1
- 出典データセット
- uspto-grants-1985_08
- 特許番号
- US04536501
反応ノート
読み込み中…