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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 566875생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물4-(Piperazin-1-yl)benzene-1-sulfonamideHCID 901897—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carbaldehydeHCID 10773638—
용매TetrahydrofuranHCID 8028—
생성물4-[4-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-piperazin-1-yl]-benzenesulfonamideHCID 212639034.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06177422B1
출처 데이터셋uspto-grants-2001_01
ORD IDord-d0c80c34be8242cfb1bf393155c62d2b
출처 메모uspto-grants-2001_01