Triethylamine → 2-[(4'-Methoxy[1,1'-biphenyl]-4-yl)sulfonyl]amino-4-hydroxy-5-[(2-thiazolyl)thio]-pentanoic Acid
反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([S:15]([NH:18][CH:19]([CH2:24][CH:25]3[O:27][CH2:26]3)[C:20]([O:22]C)=[O:21])(=[O:17])=[O:16])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.CCN(CC)CC.[SH:35][C:36]1[S:37][CH:38]=[CH:39][N:40]=1>C1C=CC=CC=1.O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[CH:11][C:12]([S:15]([NH:18][CH:19]([CH2:24][CH:25]([OH:27])[CH2:26][S:35][C:36]3[S:37][CH:38]=[CH:39][N:40]=3)[C:20]([OH:22])=[O:21])(=[O:17])=[O:16])=[CH:13][CH:14]=2)=[CH:5][CH:4]=1参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of methyl 2-[(4′-methoxy[1,1′-biphenyl]-4-yl)sulfonyl]amino-4,5-epoxypentanoate 1d (0.7 g, 1.79 mmol) in benzene (5 mL) and Et3N (0.33 mL, 2.3 mmol) at room temperature is added slowly 2-mercaptothiazole (0.52 g, 4.48 mmol). The reaction mixture is stirred for 4 h at room temperature. The resulting mixture is diluted with water, and the mixture is then extracted three times with EtOAc. The combined EtOAc layer is consecutively washed with water, and brine, dried over MgSO4 and concentrated to an oil under reduced pressure. Purification is accomplished by column chromatography with hexane/EtOAc (4:1 to 7:3 to 6:4) eluent to give the desired product.
後処理
- extractionthe mixture is then extracted three times with EtOAc
- washThe combined EtOAc layer is consecutively washed with water, and brine
- dry with materialdried over MgSO4
- concentrationconcentrated to an oil under reduced pressure
- customPurification
出典と根拠
- ORDレコード
- ord-ab1c37af08ed4c42af1536ea8a727798
- 出典データセット
- uspto-grants-2003_05
- 特許番号
- US06566381B1
反応ノート
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