Tetrahydrofuran → (5-{5-[3-Chloro-4-(3-fluorophenoxy)phenyl]-1,2,4-oxadiazol-3-yl}-4-ethyl-2-thienyl)methanol
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=1)[C:5]([OH:7])=O.ON1C2C=CC=CC=2N=N1.Cl.C(N=C=NCCCN(C)C)C.[Si]([O:48][CH2:49][C:50]1[S:54][C:53]([C:55](=[N:57]O)[NH2:56])=[C:52]([CH2:59][CH3:60])[CH:51]=1)(C(C)(C)C)(C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC.O1CCCC1>>[Cl:1][C:2]1[CH:3]=[C:4]([C:5]2[O:7][N:57]=[C:55]([C:53]3[S:54][C:50]([CH2:49][OH:48])=[CH:51][C:52]=3[CH2:59][CH3:60])[N:56]=2)[CH:8]=[CH:9][C:10]=1[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([F:18])[CH:13]=1参加物
反応物 6
生成物 1
実験手順
The crude product of the title compound was synthesized by conducting the reaction similar to that mentioned in Example 5 (5a) using 3-chloro-4-(3-fluorophenoxy)benzoic acid (0.14 g, 0.53 mmol) that was obtained in Example 16 (16a), 1-hydroxybenzotriazole (0.086 g, 0.56 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.11 g, 0.56 mmol), 5-({[t-butyl(dimethyl)silyl]oxy}methyl)-3-ethyl-N′-hydroxythiophene-2-carboximidamide (0.16 g, 0.51 mmol) that was obtained in Example 10 (10d), and 1.0M solution of tetrabutylammoniumfluoride in tetrahydrofuran (1.0 mL, 1.0 mmol). Subsequently, the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (2:8 to 5:5) as the eluent to afford the title compound (0.17 g) in a yield of 89% as a pale yellowish crystalline solid.
後処理
- customthe reaction similar to
出典と根拠
- ORDレコード
- ord-fff068e8a2244f0b9e0fb9b52d8ee061
- 出典データセット
- uspto-grants-2010_03
- 特許番号
- US07687491B2
反応ノート
読み込み中…