Hydrochloric Acid → cis 5,6-dihydro-6-(2-ethoxycarbonylethyl)-4-(4-methoxybenzylamino)-4H-thieno[2,3-b]thiopyran
反応式
O=[C:2]1[CH:7](CCC(OCC)=O)[CH2:6][S:5][C:4]2[S:15][CH:16]=[CH:17][C:3]1=2.[CH3:18][O:19][C:20]1[CH:27]=[CH:26][C:23]([CH2:24][NH2:25])=[CH:22][CH:21]=1.[BH4-].[Na+].Cl.[CH3:31][CH2:32][OH:33]>C1COCC1.C1(C)C=CC=CC=1.[Ti](Cl)(Cl)(Cl)Cl>[CH2:32]([O:33][C:20]([CH2:21][CH2:22][C@H:6]1[S:5][C:4]2[S:15][CH:16]=[CH:17][C:3]=2[C@@H:2]([NH:25][CH2:24][C:23]2[CH:26]=[CH:27][C:20]([O:19][CH3:18])=[CH:21][CH:22]=2)[CH2:7]1)=[O:19])[CH3:31]参加物
9
反応物 5
生成物 1
試薬・触媒・溶媒 3
実験手順
To a solution of 2 (10.4 g, 0.039 mol) in THF (110 ml) and toluene (110 ml) at 0° is added 4-methoxybenzylamine (25.5 ml, 26.8 g, 0.195 mol). Titanium tetrachloride (2.2 ml, 3.8 g, 0.02 mol) is added to the cold solution and the resulting mixture is stirred for 0.75-1 hour. The mixture is added to a cold (0°) stirred suspension of NaBH4 (4.5 g, 0.12 mol) in EtOH (900 ml). The resulting mixture is stirred for about 1 hour and acidified to pH 1 with 3N HCl. The solvent is removed in vacuo and the residue partitioned between EtOAc and saturated NaHCO3 solution. The EtOAc layer is separated, dried and concentrated to dryness to yield 3 wherein R1, R2, R3 and R4 are each H.
後処理
- additionThe mixture is added to a cold (0°)
- stirringstirred
- stirringThe resulting mixture is stirred for about 1 hour
- customThe solvent is removed in vacuo
- customthe residue partitioned between EtOAc and saturated NaHCO3 solution
- customThe EtOAc layer is separated
- customdried
- concentrationconcentrated to dryness
- customto yield 3 wherein R1, R2, R3 and R4
出典と根拠
- ORDレコード
- ord-68e0aeaf7c0440b7bf7780fc3524c4be
- 出典データセット
- uspto-grants-1993_08
- 特許番号
- US05235059
反応ノート
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