Dichloromethane → 5-chloro-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amine
反応式
[Cl:1][C:2]1[C:3]([F:14])=[C:4]2[C:10]([N+:11]([O-])=O)=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1.Cl[Sn]Cl.[OH-].[Na+].C(Cl)Cl>Cl>[Cl:1][C:2]1[C:3]([F:14])=[C:4]2[C:10]([NH2:11])=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1参加物
6
実験手順
5-Chloro-4-fluoro-3-nitro-1H-pyrrolo[2,3-b]pyridine (1.20 g, 5.57 mmol) was placed in 6M HCl (30 mL). SnCl2 (5.28 g, 27.8 mmol) was then added, and the reaction was stirred for 30 minutes at room temperature. The reaction was then poured into a mixture of 1M NaOH and ice. The resulting suspension was then raised to a pH of 8 and then extracted with 3:1 DCM:i-PrOH. The combined organic fractions were dried, filtered, and concentrated to give the crude product, which was triturated with 10:1 hexanes:DCM to give the product 5-chloro-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-amine (0.8 g, 77% yield).
後処理
- temperatureThe resulting suspension was then raised to a pH of 8
- extractionextracted with 3:1 DCM
- customThe combined organic fractions were dried
- filtrationfiltered
- concentrationconcentrated
- customto give the crude product, which
- customwas triturated with 10:1 hexanes
出典と根拠
- ORDレコード
- ord-d35158486eff4e71b8b418e0bd0e126c
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08981085B2
反応ノート
読み込み中…