反応式
[F:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:18]=[C:17]([C:19]([OH:21])=O)[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[N:10]=2)[CH:5]=[CH:6][C:7]=1[F:8].F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)[C:33]2[CH:34]=[CH:35][CH:36]=C[C:32]=2[N:31]=N1.C([O-])(O)=[O:50].[Na+]>CN(C=O)C>[F:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:18]=[C:17]([C:19]([N:31]3[CH2:32][CH2:33][CH2:34][C@@H:35]3[CH2:36][OH:50])=[O:21])[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[N:10]=2)[CH:5]=[CH:6][C:7]=1[F:8]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of 2-(3,4-difluoroPhenyl)-4-quinoline carboxylic acid (100 mg), BOP (220 mg) and (R)-(−)-pyrrolidine methanol (0.1 mL) in 1 ml of DMF is stirred at room temperature for 18 hours. The mixture is added to saturated aqueous NaHCO3 solution and extracted three times with EtOAc. The combined EtOAc layers are washed with brine and water, dried over Na2SO4, filtered and concentrated to afford a foam. The foam is purified by preparative silica gel thin layer chromatography, using 10% methanol in methylene chloride as the developing solvent. The desired product is obtained as a free base. 1H NMR (CDCl3) d 1.77 -1.87(3H, m), 2.16-2.22 (1H, m), 3.18-3.26 (2H, m), 3.83-3.95 (2H, m), 4.52-4.56 (1H, m), 7.23-7.30 (1H, m), 7.57 (1H, m), 7.73-7.78 (2H, m), 7.83 (1H, d), 7.87 (1H, m), 8.03-8.10 (1H, m), 8.15 (1H, d). The hydrochloride salt was prepared by treating the free base in EtOAc with a solution of hydrogen chloride in ether and collecting the resulting solid by filtration.
後処理
- extractionextracted three times with EtOAc
- washThe combined EtOAc layers are washed with brine and water
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customto afford a foam
- customThe foam is purified by preparative silica gel thin layer chromatography
出典と根拠
- ORDレコード
- ord-c38a426b38c0429fab38b282dfe34620
- 出典データセット
- uspto-grants-2003_05
- 特許番号
- US06559163B2
関連ノート
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