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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1295467생성일: 2026년 10월 26일

p-Toluenesulfonic acid → 6-chloro-8-(2,5-dimethoxybenzyl)-N9-butyl purine

https://huagongshe.com/reaction/1295467

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물N-(4-butylamino-6-chloro-pyrimidin-5-yl)-2-(2,5-dimethoxyphenyl)acetamideHCID 11660875—
용매TolueneHCID 1140—
생성물6-chloro-8-(2,5-dimethoxybenzyl)-N9-butyl purineHCID 85827657—

반응 단계

A mixture of N-(4-butylamino-6-chloro-pyrimidin-5-yl)-2-(2,5-dimethoxyphenyl) acetamide (1 mmol) and p-TSA (0.5 mmol) in toluene was refluxed for 72 h. Solvent was removed, diluted with EtOAc and washed with water, bicarbonate and dried. Purification on a silica gel column (200-400 mesh, Fisher Scientific, Tustin, Calif., USA) gave 6-chloro-8-(2,5-dimethoxybenzyl)-N9-butyl purine. Rf=0.65 in 1:1 EtOAc:hexane. 1H NMR (DMSO-d6) δ 8.7 (s, 1H), 6.96 (d, 1H), 6.84 (m, 1H), 6.8 (dd, 1H), 4.28 (s, 2H), 4.23 (t, 2H), 3.69 (s, 3H), 3.67 (s, 3H), 1.62 (m, 2H), 1.25 (m, 2H), 0.88 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07241890B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-867b123fb1914c5d8e5db6b8d90fc0cb
출처 메모uspto-grants-2007_07