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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720851생성일: 2026년 10월 26일

Diisopropylethylamine → 3-{4-[(6-{Benzyl[(2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethyl]amino}hexyl)oxy]butyl}benzenesulfonamide

https://huagongshe.com/reaction/720851

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Benzenesulfonamide, 3-[4-[(6-bromohexyl)oxy]butyl]-HCID 21895438—
반응물(1R)-2-(benzylamino)-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanolHCID 69196697—
용매Diethyl EtherHCID 3283—
용매AcetonitrileHCID 6342—
생성물3-{4-[(6-{Benzyl[(2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethyl]amino}hexyl)oxy]butyl}benzenesulfonamideHCID 69198625113.1%

반응 단계

A stirred mixture of 3-{4-[(6-bromohexyl)oxy]butyl}benzenesulfonamide (11.1 g), (1R)-2-(benzylamino)-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanol (9 g) and diisopropyl ethylamine (8.9 ml) in acetonitrile (28 ml) was heated at reflux for 18 h. The resulting mixture was cooled to room temperature, diluted with diethyl ether (250 ml) and washed with water (2×100 ml) and brine (100 ml) before being dried over anhydrous Na2SO4. The suspension was filtered and concentrated under reduced pressure to give the title compound (20 g) as an oil. LC RT=4.68 min, δ (CDCl3) 7.70 (2H, m), 7.38 (2H, m), 7.29 (5H, m), 7.02 (1H, d, J 8.3 Hz), 6.91 (1H, s), 6.73 (1H, d, J 8.3 Hz), 4.79 (2H, s), 4.53 (1H, m), 3.87 (1H, m), 3.40 (5H, m), 2.69 (2H, t, J 7.2 Hz), 2.54 (2H, m), 2.43 (2H, m), 1.70 (2H, m), 1.60 (2H, m), 1.51 (10H, m), 1.25 (4H, m)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135600B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-6d8d3730661944749e465230f037fb60
출처 메모uspto-grants-2006_11