Triethylamine → Imidazo[1,2-a]pyridine-6-carboxylic acid (5-(3-chloro-phenoxy)-thiophen-2-ylmethyl)-amide
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][CH:15]=1)[O:5][C:6]1[S:10][C:9]([CH2:11][NH2:12])=[CH:8][CH:7]=1.[N:16]1[CH:17]=[CH:18][N:19]2[CH:24]=[C:23]([C:25](O)=[O:26])[CH:22]=[CH:21][C:20]=12.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.C(N(CC)CC)C>CN(C)C=O.O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][CH:15]=1)[O:5][C:6]1[S:10][C:9]([CH2:11][NH:12][C:25]([C:23]2[CH:22]=[CH:21][C:20]3[N:19]([CH:18]=[CH:17][N:16]=3)[CH:24]=2)=[O:26])=[CH:8][CH:7]=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 C-(5-(3-chloro-phenoxy)-thiophen-2-yl)-methylamine described in Preparation Example 167 (104 mg, 0.434 mmol) and imidazo[1,2-a]pyridine-6-carboxylic acid (77 mg, 0.477 mmol) in N,N-dimethylformamide (3 mL) were added benzotriazol-1-yloxy tris(dimethylamino)phosphonium hexafluorophosphate (250 mg, 0.564 mmol) and triethylamine (181 μL) at room temperature, and the solution was stirred at room temperature for 4 hours. Water was added to the reaction solution, which was then extracted with ethyl acetate, and the organic layer was washed with water and brine. Anhydrous magnesium sulfate was added to the organic layer for drying, filtration was carried out, then, the solvent was evaporated in vacuo, the residue was purified by NH silica gel column chromatography (ethyl acetate/methanol=40/1), and the title compound (149 mg, 89%) was obtained as a white solid.
後処理
- extractionwas then extracted with ethyl acetate
- washthe organic layer was washed with water and brine
- additionAnhydrous magnesium sulfate was added to the organic layer
- customfor drying
- filtrationfiltration
- customthe solvent was evaporated in vacuo
- customthe residue was purified by NH silica gel column chromatography (ethyl acetate/methanol=40/1)
出典と根拠
- ORDレコード
- ord-acf750ea5c1447968b379fa3692dce42
- 出典データセット
- uspto-grants-2011_04
- 特許番号
- US07932272B2
反応ノート
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