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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1156267생성일: 2026년 10월 27일

5-Nitroso-2,4,6-pyrimidinetriamine → 2,4,7-Triamino-6-(p-acetoxyphenyl)-pteridine

https://huagongshe.com/reaction/1156267

반응식

참여 물질

역할이름HCID투입량
반응물5-Nitroso-2,4,6-pyrimidinetriamineHCID 70504—
반응물SodiumHCID 5360545—
반응물p-AcetoxybenzylcyanideHCID 15628731—
용매Glycol monoethyl etherHCID 8076—
생성물2,4,7-Triamino-6-(p-acetoxyphenyl)-pteridineHCID 20535715—

반응 단계

410 mg metallic sodium were dissolved while stirring in 100 ml of 2-ethoxy ethanol. Thereafter, 1100 mg 2,4,6-Triaminonitrosopyrimidine are added while stirring together with 1140 mg p-acetoxybenzylcyanide and the mixture is heated while stirring up to the boiling point. The color of the mixture changed from violet to brown. After two hours boiling under reflux, the heat is turned off and the reaction mixture is allowed to cool. Thereafter, 70 to 80% of the 2-ethoxyethanol is distilled under the vacuum of the water system, and the residue is taken up in 500 mls of water. After four-fold extraction with ether the pH is adjusted to pH 5 with 2 N hydrochloric acid. The precipitate is filtered, it is washed with a small amount of ice-cold acetone and recrystallized from 10% acetic acid. Further purification can be carried out over a silica gel column. The title compound obtained melts at 319°-321° C. (carbonization).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04335119
출처 데이터셋uspto-grants-1982_06
ORD IDord-55bfc357f67043e7bcb11c0e856a2e0e
출처 메모uspto-grants-1982_06