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HRID 2164541作成日:2026年10月26日

Acetic Acid → 6-chloro-2,3-dihydro-3-oxo-2-(2-pyridinylmethyl)-1H-isoindole-5-sulfonamide hydrochloride

https://huagongshe.com/reaction/2164541

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Hydrochloric AcidHCID 313—
反応物PhthalimideHCID 6809—
反応物6-Chloro-2,3-dihydro-1,3-dioxo-2-(2-pyridinylmethyl)-1H-isoindole-5-sulfonamideHCID 13473183—
触媒ZincHCID 23994—
触媒ZINC acetic acidHCID 57475673—
溶媒DimethylformamideHCID 6228—
生成物6-chloro-2,3-dihydro-3-oxo-2-(2-pyridinylmethyl)-1H-isoindole-5-sulfonamide hydrochlorideHCID 20404852—

反応手順

Zinc-acetic acid reduction of 6-chloro-2,3-dihydro-1,3-dioxo-2-(2-pyridinylmethyl)-1H-isoindole-5-sulfonamide. Zinc dust (0.5 mole) is added in one portion to the 1,3-dioxoisoindole (0.1 mole) of part (a) in 800 ml. of acetic acid. The reaction mixture is stirred at room temperature for 1.0 hr. and then heated to reflux for a 6 hr. period during which time additional 9.0 g. portions of zinc are added at the end of 3, 4, and 5 hr., respectively. After stirring overnight, the reaction mixture is filtered and the filtrate concentrated to dryness under reduced pressure with additional water added to the residue and removed in vacuo to remove traces of acetic acid. Residual material is slurried in water, filtered, and the filtrate concentrated to dryness. Residual material is stirred with saturated sodium bicarbonate solution and an immiscible organic solvent such as hot ethyl acetate. The organic fraction is separated, dried over MgSO4 and concentrated to provide the product as the free base. The free base taken up in dimethylformamide and acidified with ethanolic hydrogen chloride affords 6-chloro-2,3-dihydro-3-oxo-2-(2-pyridinylmethyl)-1H-isoindole-5-sulfonamide hydrochloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04505911
出典データセットuspto-grants-1985_03
ORD IDord-9415240d1fc74991ab09c1626e1fa663
出典メモuspto-grants-1985_03