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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1024559생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1024559

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물D-ValinolHCID 6950587—
반응물6-chloro-3-(2-ethoxy-3,4-dioxo-cyclobut-1-enylamino)-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamideHCID 56844293—
용매EthanolHCID 702—
생성물6-Chloro-2-hydroxy-N-methoxy-3-[2-((R)-1-methoxymethyl-2-methyl-propylamino)-3,4-dioxo-cyclobut-1-enylamino]-N-methyl-benzenesulfonamideHCID 44629149—

반응 조건

온도85 °C

반응 단계

To a stirred solution of triethylamine (1.192 ml, 8.55 mmol) and (R)-2-Amino-3-methyl-butan-1-ol (Intermediate H) in EtOH (36 ml) was added 6-chloro-3-(2-ethoxy-3,4-dioxo-cyclobut-1-enylamino)-2-hydroxy-N-methoxy-N-methyl-benzenesulfonamide (Intermediate A) (1.67 g, 4.27 mmol). The reaction mixture was heated at 85° C. for 18 hours. The reaction mixture was concentrated in vacuo and dissolved in EtOAc. The EtOAc solution was washed with 1M HCl (aq) and NaHCO3 (aq). The NaHCO3 (aq) layer was extracted with EtOAc. The EtOAc layers were combined and concentrated in vacuo. The residue was purified using flash chromatography (0-10% MeOH in DCM) to furnish a brown solid [M+H]+ 462.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722925B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-16d6a2464d914e778632e25b7c50c17e
출처 메모uspto-grants-2014_05