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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1262519생성일: 2026년 10월 27일

Hydrochloric Acid → 4-(1,3-diethyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)benzenesulfonic acid

https://huagongshe.com/reaction/1262519

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물5,6-Diamino-1,3-diethyluracilHCID 4572133—
반응물Potassium 4-carboxybenzenesulfonateHCID 23670833—
용매WaterHCID 962—
생성물4-(1,3-diethyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)benzenesulfonic acidHCID 1558730067.6%

반응 단계

A mixture of 5,6-diamino-1,3-diethyl-2,4(1H,3H)-pyrimidinedione (41.2 g, 0.208 moles), 4-sulfobenzoic acid monopotassium salt (50.0 g, 0.208 moles), and water (250 ml) is prepared, and the pH adjusted to 6.0. Ethyl-3-(3-dimethylaminopropyl)carbodiimide (39.9 g, 0.208 moles) is added in one portion, and the pH of the resulting solution maintained at 5.5±0.5 with the dropwise addition of 4 N hydrochloric acid. When the pH of the solution ceases to rise, the mixture is concentrated on a rotary evaporator, and the residue taken up in 400 ml 10% potassium hydroxide and stirred for 18 hours. At the end of this time, the solution is boiled under reflux for one hour, cooled, filtered, and made acidic with the portionwise addition of 12 N hydrochloric acid. The resulting suspension is cooled and filtered; the solids are triturated with ethanol, filtered, and dried to yield 51.2 grams of 4-(1,3-diethyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)-benzenesulfonic acid; mp greater than 360° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04452788
출처 데이터셋uspto-grants-1984_06
ORD IDord-081a38aa30294bcbab0cad4c11d72b5b
출처 메모uspto-grants-1984_06