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HRID 566875作成日:2026年10月26日

4-(Piperazin-1-yl)benzene-1-sulfonamide → 4-[4-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-piperazin-1-yl]-benzenesulfonamide

https://huagongshe.com/reaction/566875

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Piperazin-1-yl)benzene-1-sulfonamideHCID 901897—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carbaldehydeHCID 10773638—
溶媒TetrahydrofuranHCID 8028—
生成物4-[4-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-piperazin-1-yl]-benzenesulfonamideHCID 212639034.4%

反応手順

Sodium triacetoxyborohydride (1.2 g, 5.9 mmol) is added to a solution of 3-oxo-3,4-dihydro-2H-benzo[1,4]-oxazine-6-carbaldehyde (0.5 g, 2.8 mmol) and 4-(piperazin-1-yl)-benzenesulfonamide (0.17 g, 3.1 mmol) in 20 mL of THF. The mixture is stirred at room temperature overnight. The reaction is quenched by addition of 50 mL of water, and the THF is removed under reduced pressure. The precipitate is collected by filtration and recrystallized from methanol to give 0.05 g (4% yield) of 4-[4-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-piperazin-1-yl]-benzenesulfonamide; mp 150-153° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06177422B1
出典データセットuspto-grants-2001_01
ORD IDord-d0c80c34be8242cfb1bf393155c62d2b
出典メモuspto-grants-2001_01