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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23342생성일: 2026년 10월 24일

Triphenylphosphine → Phenyl-[6-(tetrahydrofuran-3-(R)-yl-oxy)quinoxalin-2-yl]amine

https://huagongshe.com/ko/reaction/23342

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물(S)-(+)-3-HydroxytetrahydrofuranHCID 2733227—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물2-Anilino-6-quinoxalinolHCID 135512461—
용매TetrahydrofuranHCID 8028—
생성물Phenyl-[6-(tetrahydrofuran-3-(R)-yl-oxy)quinoxalin-2-yl]amineHCID 22898590—

반응 단계

To a THF solution at 0° C. under argon is added 2-anilino-6-quinoxalinol (0.23 g, 0.97 mmol), (S)-(+)-3-hydroxytetrahydrofuran (0.086 mL, 1.3 mmol), and triphenylphosphine (0.31 g, 1.2 mmol). DEAD (0.18 mL, 1.2 mmol) is added portionwise. The reaction is allowed to warm to room temperature and stirred for 1.5 hours. The mixture is concentrated and partitioned between EtOAc and H2O. The organic layer is washed with H2O, brine, dried (MgSO4), and concentrated. The resulting yellow oil is chromatographed (50% EtOAc/hexanes) and taken up in Et2O/IPA. HCl/Et2O solution is added dropwise and the resulting red-orange powder is dried in vacuo. The powder is free-based by stirring in MeOH with washed (3×H2O, 5×MeOHM basic ion exchange resin. The mixture is stirred 30 minutes, filtered, concentrated, and recrystallized from EtOAc/hexanes to provide, in two crops, the product (m.p. 173-175° C.). Anal. Calcd. for C18H17N3O2: C, 70.35; H, 5.57; N, 13.67; Found: C, 70.19; H, 5.60; N, 13.66.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852712B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-e871bfab0a334f8bb89e79609cb3f075
출처 메모uspto-grants-2005_02