Water → Methyl 3-(cyclopropylamino)-5-[(4-fluorophenyl)methyl]-2-pyridinecarboxylate
反応式
[CH:1]1([NH:4][C:5]2[C:6]([C:19]([OH:21])=[O:20])=[N:7][CH:8]=[C:9]([CH2:11][C:12]3[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=3)[CH:10]=2)[CH2:3][CH2:2]1.[C:22](=O)([O-])[O-].[K+].[K+].CI.O>CN(C=O)C.C(OCC)(=O)C>[CH:1]1([NH:4][C:5]2[C:6]([C:19]([O:21][CH3:22])=[O:20])=[N:7][CH:8]=[C:9]([CH2:11][C:12]3[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=3)[CH:10]=2)[CH2:2][CH2:3]1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of 3-(cyclopropylamino)-5-[(4-fluorophenyl)methyl]-2-pyridinecarboxylic acid (298 mg, 1.1 mmol) in DMF (10 mL) was added potassium carbonate (316 mg, 2.3 mmol) followed by methyl iodide (0.15 mL, 2.3 mmol). The resultant suspension was stirred for 1.5 hours at which time water and ethyl acetate were added. The layers were separated and the organic layer was washed with brine. The aqueous layer was extracted with ethyl acetate and the combined organics were dried over sodium sulphate. Filtration and concentration followed by purification by silica gel chromatography provided methyl 3-(cyclopropylamino)-5-[(4-fluorophenyl)methyl]-2-pyridinecarboxylate (234 mg, 77%) as a white crystalline solid upon standing. 1H NMR (400 MHz, CDCl3) δ 7.90 (d, J=1.9 Hz, 1 H), 7.78 (br, 1 H), 7.24 (s, 1 H), 7.15 (dd, J=8.5, 5.4 Hz, 2 H), 7.00 (t, J=8.7 Hz, 2 H), 3.96 (s, 2 H), 3.93 (s, 3 H), 2.39 (m, 1 H), 0.77 (m, 2 H), 0.52 (m, 2 H); MS m/z 301 (M+1).
後処理
- additionwere added
- customThe layers were separated
- washthe organic layer was washed with brine
- extractionThe aqueous layer was extracted with ethyl acetate
- dry with materialthe combined organics were dried over sodium sulphate
- filtrationFiltration and concentration
- customfollowed by purification by silica gel chromatography
出典と根拠
- ORDレコード
- ord-863cb6821c464aaf8f68a4a4ff02bf87
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08691991B2
反応ノート
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