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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 386181생성일: 2026년 10월 25일

Phthalimide → 2-[(3-Chloropyrazin-2-yl)-quinolin-7-ylmethyl]-isoindole-1,3-dione

https://huagongshe.com/reaction/386181

반응식

참여 물질

역할이름HCID투입량
반응물PhthalimideHCID 6809—
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물(3-Chloropyrazin-2-yl)-quinolin-7-ylmethanolHCID 57680924—
용매TetrahydrofuranHCID 8028—
생성물2-[(3-Chloropyrazin-2-yl)-quinolin-7-ylmethyl]-isoindole-1,3-dioneHCID 53629024—

반응 단계

To a suspension of (3-chloropyrazin-2-yl)-quinolin-7-ylmethanol (600 mg, 2.21 mmol), phthalimide (356 mg, 2.42 mmol), and PS—PPh3 (loading 2.12 mmol/g; 1.56 g, 3.31 mmol) in dry THF (20 mL), cooled by ice/water, was added DIAD (480 μL, 493 mg, 2.44 mmol), then the cooling bath was removed and the flask was vortexed at ambient temperature for 21.5 h. More PS—PPh3 (520 mg, 1.10 mmol) and DIAD (160 μL, 164 mg, 0.81 mmol) were added, and vortexing was continued for 6.5 h. The resin was filtered and washed with THF and CH2Cl2. The crude material was chromatographed on silica gel [Jones Flashmaster, 20 g/70 mL cartridge, eluting with hexanes:EtOAc 3:1 (1-14)→2:1 (15-29)→1:1 (30-65)→1:2 (66-80)], yielding the title compound as pale yellow solid; 1H NMR (CDCl3, 400 MHz) δ 7.12 (s, 1H), 7.41 (dd, J=4.4, 8.0 Hz, 1H), 7.54 (dd, J=2.0, 8.4 Hz, 1H), 7.72-7.78 (m, 2H), 7.81-7.89 (m, 3H), 8.01 (d, J=0.8 Hz, 1H), 8.16 (dd, J=0.8, 8.4 Hz, 1H), 8.39 (d, J=2.4 Hz, 1H), 8.50 (d, J=2.4 Hz, 1H), 8.90 (dd, J=1.6, 4.2 Hz, 1H); MS (ES+): m/z 401.0/402.9 (100/38) [MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367826B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-ce1b0fbb64694d959a2161ef75989416
출처 메모uspto-grants-2013_02