Hydrochloric Acid → 2-(1,3-Dioxo-1,3-dihydroisoindol-2-yl)-4-(2-methoxyphenyl)-thiophene-3-carboxylic acid
反応式
[OH-].[Na+].CO.C([O:7][C:8]([C:10]1[C:14]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[O:21][CH3:22])=[CH:13][S:12][C:11]=1[N:23]1[C:31](=[O:32])[C:30]2[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=2)[C:24]1=[O:33])=[O:9])C.Cl>O>[O:32]=[C:31]1[C:30]2[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=2)[C:24](=[O:33])[N:23]1[C:11]1[S:12][CH:13]=[C:14]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[O:21][CH3:22])[C:10]=1[C:8]([OH:9])=[O:7]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of NaOH (1.4 mmol) in a 1:1 mixture of methanol:H2O (6 mL) is added 2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-(2-methoxyphenyl)-thiophene-3-carboxylic acid ethyl ester (0.7 mmol, Example 17, Part C). The mixture is heated to reflux for 90 minutes, then diluted with water (12 mL), chilled in an ice bath, and acidified with concentrated HCl. The product that precipitates is collected by filtration, washed with water, and dried, affording the desired compound.
後処理
- temperatureThe mixture is heated
- temperatureto reflux for 90 minutes
- temperaturechilled in an ice bath
- customThe product that precipitates
- filtrationis collected by filtration
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-ef2b00e5a2504e39a268105c189b1b69
- 出典データセット
- uspto-grants-2006_09
- 特許番号
- US07101905B2
反応ノート
読み込み中…