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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943831생성일: 2026년 10월 26일

Iodoethane → 3-butyl-1-ethyl-7-(phenylmethyl)-3,7-dihydro-1H-purine-2,6-dione

https://huagongshe.com/reaction/1943831

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Potassium CarbonateHCID 11430—
반응물7-Benzyl-3-butylxanthineHCID 3993866—
용매DimethylformamideHCID 6228—
생성물3-butyl-1-ethyl-7-(phenylmethyl)-3,7-dihydro-1H-purine-2,6-dioneHCID 59299554—

반응 단계

3-butyl-7-(phenylmethyl)-3,7-dihydro-1H-purine-2,6-dione (0.429 g, 1.24 mmol) and potassium carbonate (0.256 g, 1.85 mmol) were suspended in DMF (8 mL), iodoethane (0.113 mL, 1.42 mmol) was added. The reaction mixture was stirred at ambient temperature overnight. The reaction mixture was evaporated to dryness and the residue was partitioned between water and ethyl acetate. The organic layer was washed with water, followed by brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to yield the title compound; 1H NMR (400 MHz; CDCl3) δ: 0.96 (3H, t), 1.25 (3H, t), 1.36-1.45 (2H, m), 1.72-1.76 (2H, m), 4.05-4.13 (4H, m), 5.50 (2H, s), 7.32-7.40 (5H, m), 7.52 (1H, s); m/z 327[MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08394808B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-9c3f344b3dfb45189245a75f78713d0d
출처 메모uspto-grants-2013_03