Acetic Acid → 6-chloro-2,3-dihydro-1-hydroxy-3-oxo-2-[1-[[3-(trifluoromethyl)phenyl]methyl]-4-piperidinyl]-1H-isoindole-5-sulfonamide
反応式
O=C1C2C(=CC=CC=2)C(=O)N1.[Cl:12][C:13]1[CH:21]=[C:20]2[C:16]([C:17](=[O:40])[N:18]([CH:23]3[CH2:28][CH2:27][N:26]([CH2:29][C:30]4[CH:35]=[CH:34][CH:33]=[C:32]([C:36]([F:39])([F:38])[F:37])[CH:31]=4)[CH2:25][CH2:24]3)[C:19]2=[O:22])=[CH:15][C:14]=1[S:41]([NH2:44])(=[O:43])=[O:42].C(O)(=O)C>C(OCC)(=O)C>[Cl:12][C:13]1[CH:21]=[C:20]2[C:16]([C:17](=[O:40])[N:18]([CH:23]3[CH2:24][CH2:25][N:26]([CH2:29][C:30]4[CH:35]=[CH:34][CH:33]=[C:32]([C:36]([F:38])([F:37])[F:39])[CH:31]=4)[CH2:27][CH2:28]3)[CH:19]2[OH:22])=[CH:15][C:14]=1[S:41]([NH2:44])(=[O:43])=[O:42]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of the 1,3-dioxoisoindole of part (a), (8.1 g., 0.0161 mole), zinc dust (5.78 g., 0.088 mole) and 150 ml. of acetic acid was stirred for 0.5 hr. at 50°-70°, cooled. Residual material, obtained by concentration of the filtrate in vacuo, was dissolved in ethyl acetate and washed with saturated sodium bicarbonate solution and the aqueous layer re-extracted with ethyl acetate. Combined extracts were washed with saturated sodium bicarbonate, dried (MgSO4) and concentrated in vacuo. Trituration of the residue with ethyl acetate provided 6-chloro-2,3-dihydro-1-hydroxy-3-oxo-2-[1-[[3-(trifluoromethyl)phenyl]methyl]-4-piperidinyl]-1H-isoindole-5-sulfonamide as a white solid, m.p. 204°-205°.
後処理
- temperatureat 50°-70°, cooled
- customResidual material, obtained by concentration of the filtrate in vacuo
- washwashed with saturated sodium bicarbonate solution
- extractionthe aqueous layer re-extracted with ethyl acetate
- washCombined extracts were washed with saturated sodium bicarbonate
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-5f42b402a5e44adaa85c914c03eb7664
- 出典データセット
- uspto-grants-1986_07
- 特許番号
- US04600758
反応ノート
読み込み中…