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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 467222생성일: 2026년 10월 26일

6-Benzyloxyamino-4-chloro-2,5-diformamidopyrimidine → 9-Benzyloxy-6-chloro-2-formamidopurine

https://huagongshe.com/reaction/467222

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참여 물질

역할이름HCID투입량
반응물6-Benzyloxyamino-4-chloro-2,5-diformamidopyrimidineHCID 14523960—
용매Methanol, 1,1-diethoxy-, 1-acetateHCID 84166—
생성물9-Benzyloxy-6-chloro-2-formamidopurineHCID 1452396162%

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온도20 °C

반응 단계

6-Benzyloxyamino-4-chloro-2,5-diformamidopyrimidine (1.2g, 3.73mmol) and diethoxymethyl acetate (20ml) was stirred at 120° C. for 2.5 hours, cooled and evaporated under reduced pressure. The residue in methanol (20ml) and concentrated ammonia solution (2ml) was stirred at 20° C. for 1 hour, the solvent removed under reduced pressure and the residue co-evaporated with methanol. Column chromatography on silica gel (eluted with chloroform-ethanol, 100:1) afforded the title compound (700mg, 62%). IR: υmax (KBr) 3119, 1702, 1611, 1577, 1505, 1440cm-1 ; 1H NMR: δH [(CD3)2SO], 5.44 (2H, s, CH2Ph), 7.45 (5H, m, Ph), 8.54 (1H, s, H-8), 9.34 (1H, s, CHO), 11.30 (1H, br.s, D2O exchangeable, NH). Found: C, 49.99; H, 3.37; N, 22.43%, m/e 303.0523. C13H10N5O2Cl + 0.5 H2O requires: C, 49.92; H, 3.55; N, 22.40%, m/e 303.0520.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05159076
출처 데이터셋uspto-grants-1992_10
ORD IDord-0fac7c69adb44b7abce2b759c79d55c7
출처 메모uspto-grants-1992_10