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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34440생성일: 2026년 10월 24일

3-Chloro-1,1-diethoxypropane → 2,4-Diamino-5-(3-(3,3-diethoxypropoxy)-4,5-dimethoxybenzyl)pyrimidine

https://huagongshe.com/ko/reaction/34440

반응식

참여 물질

역할이름HCID투입량
반응물3-Chloro-1,1-diethoxypropaneHCID 96217—
반응물3-DemethyltrimethoprimHCID 12849769—
반응물Potassium tert-butoxideHCID 23665647—
용매Dimethyl SulfoxideHCID 679—
생성물2,4-Diamino-5-(3-(3,3-diethoxypropoxy)-4,5-dimethoxybenzyl)pyrimidineHCID 1284977083%

반응 단계

To a solution of 27.6 g, (0.1 mole) of 2,4-diamino-5-(3-hydroxy-4,5-dimethoxybenzyl)pyrimidine (D. E. Schwartz, W. Vetter, and G. Englert, Arzneim.-Forsch. (Drug Res.) 1970, 20, 1867; G. Rey-Bellet and R. Reiner, Helv. Chim. Acta 1970, 53, 945) in 400 mL of dry dimethyl sulfoxide was added 11.22 g (0.10 mole) of potassium t-butoxide. To the resulting suspension was added dropwise 17.92 g (0.107 mole) of β-chloropropionaldehyde diethylacetal. The mixture was heated at 65° overnight. The solvent was removed under vacuum and the residue was partitioned between 750 mL methylene chloride and 750 mL of 0.1N sodium hydroxide. The organic layer was separated and the aqueous layer was extracted with an additional 750 mL of methylene chloride. The organic layers were combined, washed with 750 mL of water, dried (MgSO4), and purified by flash column chromatography to yield 33.38 g (83%) of the title compound (mp 105°-106.5° ). Anal. Calcd for C20H30N4O5 : C, 59.10; H, 7.44; N, 13.78. Found: C, 58.71; H, 7.40; N, 13.58.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04761475
출처 데이터셋uspto-grants-1988_08
ORD IDord-79c9ecf8ec8c48b79a4125b9f9a1d2ef
출처 메모uspto-grants-1988_08