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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1853963생성일: 2026년 10월 26일

Sodium Acetate → [6-(2-Methyl-5-nitro-phenyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amine

https://huagongshe.com/reaction/1853963

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AcetateHCID 517045—
반응물3-Dimethylaminomethylene-1-(2-methyl-5-nitrophenyl)piperidin-4-oneHCID 67328898—
반응물1-(4-(4-Methylpiperazin-1-yl)phenyl)guanidineHCID 178480747—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물[6-(2-Methyl-5-nitro-phenyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amineHCID 67328470—

반응 단계

To a solution of 3-Dimethylaminomethylene-1-(2-methyl-5-nitrophenyl)-piperidin-4-one (12.06 gm, 41.7 mmol)[as prepared in reference 1] in Ethanol (250 ml) were added N-[4-(4-Methyl-piperazin-1-yl)-phenyl]-guanidine (38.9 gm, 167 mmol) and sodium acetate (27.32 gm, 334 mmol) and solution was heated under reflux for 12 hours. After cooling to room temperature, the reaction mixture was diluted with water, extracted with ethyl acetate. The organic layer was washed with brine, dried [sodium sulfate] and concentrated under vacuum. The crude product obtained was further purified by silica gel chromatography using 5-10% Methanol/Chloroform as eluent to give pure desired product [47] i.e., [6-(2-Methyl-5-nitro-phenyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amine as yellow solid. (Yield: 3.65 gm, 19.0%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08962637B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-cb10d4bf5efb4a6e97b20e7f3b19818a
출처 메모uspto-grants-2015_02