2-Methoxyethylamine → HCID 25141526、化合物
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([C:31]([F:34])([F:33])[F:32])[O:13][N:12]=[C:11]([C:14]3[C:23]4[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=4)[C:17]([C:24]([NH:26][CH2:27][C:28](O)=[O:29])=[O:25])=[CH:16][CH:15]=3)[CH2:10]2)[CH:5]=[C:6]([Cl:8])[CH:7]=1.CC(C)(C)C(Cl)=O.[CH3:42][O:43][CH2:44][CH2:45][NH2:46].C(N(CC)CC)C>ClCCl.N1C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([C:31]([F:33])([F:34])[F:32])[O:13][N:12]=[C:11]([C:14]3[C:23]4[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=4)[C:17]([C:24]([NH:26][CH2:27][C:28]([NH:46][CH2:45][CH2:44][O:43][CH3:42])=[O:29])=[O:25])=[CH:16][CH:15]=3)[CH2:10]2)[CH:5]=[C:6]([Cl:8])[CH:7]=1参加物
実験手順
To a stirred solution of N—[[4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-1-naphthalenyl]carbonyl]glycine (i.e. the title product of Step B) (100 mg) and pyridine (0.019 mL) in dichloromethane (3 mL) was added trimethylacetyl chloride (0.029 mL). The reaction mixture was stirred at room temperature for 2 h, and then 2-methoxyethylamine (0.11 mL) and triethylamine (0.68 mL, 5.0 mmol) were added. The reaction mixture was stirred at room temperature overnight, quenched with water, extracted with dichloromethane, washed with brine, dried with anhydrous sodium sulfate and concentrated. The residue was purified by column chromatography on silica gel using hexanes/ethyl acetate (3:2 to 1:4) as eluent to afford the title compound, a compound of the present invention, as a white solid (71 mg, 0.13 mmol, 65% yield).
後処理
- stirringThe reaction mixture was stirred at room temperature overnight
- customquenched with water
- extractionextracted with dichloromethane
- washwashed with brine
- dry with materialdried with anhydrous sodium sulfate
- concentrationconcentrated
- customThe residue was purified by column chromatography on silica gel
出典と根拠
- ORDレコード
- ord-e8f81da77d894a18a2357e10b4b75e52
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09095138B2
反応ノート
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