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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 516903생성일: 2026년 10월 27일

3-Pentanamine → 6-Chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide

https://huagongshe.com/reaction/516903

반응식

참여 물질

역할이름HCID투입량
반응물3-PentanamineHCID 12019—
반응물6-chloro-3-(2-ethoxy-3,4-dioxo-cyclobut-1-enylamino)-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamideHCID 56844293—
용매TetrahydrofuranHCID 8028—
생성물6-Chloro-3-[2-(1-ethyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamideHCID 44629146—

반응 조건

온도50 °C

반응 단계

To a stirred solution of 6-chloro-3-(2-ethoxy-3,4-dioxo-cyclobut-1-enylamino)-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide (Intermediate A) (1 g, 2.56 mmol) in THF (20 ml) was added 3-aminopentane (0.596 ml, 5.12 mmol). The reaction mixture was heated at 50° C. overnight. The reaction mixture was concentrated in vacuo and dissolved in EtOAc. The EtOAc solution was washed with 1M HCl(aq) and brine. The EtOAc solution was dried (MgSO4) and concentrated in vacuo. The residue was crystallized from toluene to give a solid; [M+H]+ 432.1. 1H NMR (DMSO) 0.9 (6H, t, 2×CH3), 1.5 (2H, m), 1.6 (2H, m), 3.0 (3H, s, CH3), 3.6 (3H, s, CH3), 3.9 (1H, m), 7.2 (1H, d), 8.1 (1H, d), 8.2 (1H, d), 9.4 (1H, s), 10.1 (1H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115087B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-2fbe805f9ca845a5987c2ca4cebb3811
출처 메모uspto-grants-2015_08