戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1198646作成日:2026年10月27日

Water → N-(2-indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide

https://huagongshe.com/reaction/1198646

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-Aminoindan hydrochlorideHCID 122764—
反応物4-(N-methylacetamido)benzene-1-sulfonyl chlorideHCID 293146—
反応物Sodium AcetateHCID 517045—
溶媒EthanolHCID 702—
生成物N-(2-indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamideHCID 2291894795%

反応手順

2-Indanylamine hydrochloride (9.68 g, 57.1 mmol) was added to a suspension of the 4-(N-acetyl-N-methylamino)benzenesulfonyl chloride (12.84 g, 51.9 mmol) prepared in Preparative Example 12 and sodium acetate (18.73 g) in ethanol (100 ml). The obtained mixture was stirred at room temperature for 3 hours, followed by the addition of water. The obtained mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of common salt, dried over magnesium sulfate, and concentrated to give N-(2 indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide as a white crystal (16.92 g, 95%). Ethanol (80 ml) and 1N aqueous sodium hydroxide (80 ml) were added to the white crystal. The obtained mixture was heated under reflux overnight, acidified with 1N aqueous hydrochloric acid, adjusted to pH 8 with sodium hydrogencarbonate and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to precipitate a crystal. This crystal was recovered by filtration and washed with ether to give the title compound as a white crystal (6.79 g, 46%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05281626
出典データセットuspto-grants-1994_01
ORD IDord-431f451ec2da4f45bdabfa3305dbf7d0
出典メモuspto-grants-1994_01