Methyl 2-(4-aminopiperidin-1-yl)-1,3-thiazole-5-carboxylate → Methyl 2-(4-{[(3,4-dichloro-5-cyano-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-1,3-thiazole-5-carboxylate
反応式
[NH2:1][CH:2]1[CH2:7][CH2:6][N:5]([C:8]2[S:9][C:10]([C:13]([O:15][CH3:16])=[O:14])=[CH:11][N:12]=2)[CH2:4][CH2:3]1.[Cl:17][C:18]1[C:22]([Cl:23])=[C:21]([C:24]#[N:25])[NH:20][C:19]=1[C:26](Cl)=[O:27]>C1COCC1>[Cl:17][C:18]1[C:22]([Cl:23])=[C:21]([C:24]#[N:25])[NH:20][C:19]=1[C:26]([NH:1][CH:2]1[CH2:7][CH2:6][N:5]([C:8]2[S:9][C:10]([C:13]([O:15][CH3:16])=[O:14])=[CH:11][N:12]=2)[CH2:4][CH2:3]1)=[O:27]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
TEA (0.06 ml, 0.5 mmol) was added to a solution of methyl 2-(4-aminopiperidin-1-yl)-1,3-thiazole-5-carboxylate (Intermediate 134, 0.1 g, 0.5 mmol)) in anhydrous THF. To this was added 3,4-dichloro-5-cyano-1H-pyrrole-2-carbonyl chloride (Intermediate 132, 0.1 g, 0.5 mmol) as a solution in anhydrous THF. After stirring 15 minutes, THF was removed. The product was partitioned with EtOAc and water. The organic portion was dried with MgSO4 and concentrated to a yellow oil. Trituration with ether followed by filtration yielded a tan solid.
後処理
- customTHF was removed
- customThe product was partitioned with EtOAc and water
- dry with materialThe organic portion was dried with MgSO4
- concentrationconcentrated to a yellow oil
- filtrationTrituration with ether followed by filtration
- customyielded a tan solid
出典と根拠
- ORDレコード
- ord-cb69b010b6ec4119801c6729afda27e5
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07709503B2
反応ノート
読み込み中…