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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 742960생성일: 2026년 10월 25일

Hydrochloric Acid → 6-benzyl-3-methyl-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione

https://huagongshe.com/reaction/742960

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Hydrogen PeroxideHCID 784—
반응물Sodium HydroxideHCID 14798—
반응물6-benzyl-3-methyl-2-thioxo-2,3,5,6,7,8-hexahydropyrido[4,3-d]pyrimidin-4(1H)-oneHCID 10379323—
용매WaterHCID 962—
생성물6-benzyl-3-methyl-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dioneHCID 10016028—

반응 조건

온도0 °C

반응 단계

3.2 1 of 30% hydrogen peroxide were added dropwise at 0° C. over a period of 51/2 h, with stirring, to a suspension of 210 g of 6-benzyl-3-methyl-2-thioxo-2,3,5,6,7,8-hexahydro-1H-pyrido[4,3-d]pyrimidin-4-one from b) in a solution of 78 g of NaOH in 4 1 of water. After subsequent stirring for 1/2 hour at 0° C., the pH of 9.7 was adjusted to 7.4 with conc. hydrochloric acid and the precipitate was filtered off, washed with water and dried. The above preparation was repeated and the precipitates were combined (396 g). These were purified by suspension in I 1 of water and dissolution with 33% sodium hydroxide solution (pH 13.5). Activated charcoal was added, with stirring, the mixture was filtered and the filtrate was adjusted to pH 10. The precipitate formed was filtered off with suction, washed with water and dried under reduced pressure to give 192 g of 6-benzyl-3-methyl-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione, which was debenzylated by hydrogenolysis in d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05556854
출처 데이터셋uspto-grants-1996_09
ORD IDord-1b23f7f87a9547d7a96431a21fadb662
출처 메모uspto-grants-1996_09