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HRID 260886作成日:2026年10月27日

Acetic Acid → N-(4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide acetate

https://huagongshe.com/reaction/260886

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4-(N-methylacetamido)benzene-1-sulfonyl chlorideHCID 293146—
反応物1-Benzyl-4-piperidylamineHCID 415852—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物N-(1-Benzyl-4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamideHCID 15049722—
生成物N-(4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide acetateHCID 67690431100%

反応手順

N-(1-Benzyl-4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide was prepared as a colorless oil from the 4-(N-acetyl-N-methylamino)benzenesulfonyl chloride (20.0 g, 80.8 mmol) and 4-amino-1-benzylpiperidine (18.16 ml, 88.9 mmol) in a similar manner to that described in Preparative Example 16. This oil was dissolved in ethanol (200 ml), followed by the addition of glacial acetic acid (10.0 ml). The obtained mixture was stirred in the presence of 10% palladium/carbon (water-containing one, 2.00 g) in a hydrogen atmosphere (1 atm) at 50° C. for 5 hours and filtered to remove the catalyst. The filtrate was concentrated to precipitate a crystal. The resulting mixture was washed with ethyl acetate and filtered to give the title compound as a white crystal (29.70 g, overall yield of two steps: 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05530118
出典データセットuspto-grants-1996_06
ORD IDord-61daeb8a02174afeb1a6871e64eb89aa
出典メモuspto-grants-1996_06