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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357489생성일: 2026년 10월 23일

Acetic Acid → 2-((2-Amino-6-oxo-1,6-dihydro-9H-purin-9-YL)methoxy)-3-hydroxypropyl propionate, (+-)-

https://huagongshe.com/ko/reaction/357489

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Dimethyl SulfoxideHCID 679—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
반응물GanciclovirHCID 135398740—
용매EthanolHCID 702—
용매Ethyl orthopropionateHCID 66995—
생성물2-((2-Amino-6-oxo-1,6-dihydro-9H-purin-9-YL)methoxy)-3-hydroxypropyl propionate, (+-)-HCID 135515409—

반응 단계

To 5 g of 2-(2-amino-1,6-dihydro-6-oxo-purin-9-yl)methoxy-1,3-propanediol (ganciclovir) in 20 ml of triethyl orthopropionate was added 5 ml of dimethylsulfoxide (DMSO) and 0.25 g of pyridinium p-toluenesulfonate (PPTS). The slurry was stirred at room temperature for 4.5 hours. 70% Aqueous acetic acid (10 ml) was added and the mixture was stirred for 2 hours. Then 30 ml of ethanol was added, the mixture was stirred for another 0.5 hour and filtered. The white solid was washed twice with 50 ml each of ethanol and air dried to give 4.77 g of product. 1H-NMR: δ 0.9 (t,3H), 2.05 (q,2H), 3.32 (m,2H), 3.8 (m,1H), 3.85 (dd,1H), 4.0 (dd,1H), 4.8 (t,1H), 5.35 (ad,2H), 6.45 (br s, 2H), 7.75 (s,1H), 10.6 (s,1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840890
출처 데이터셋uspto-grants-1998_11
ORD IDord-81e27642f03d494a8ee70acca574f75e
출처 메모uspto-grants-1998_11