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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 450392생성일: 2026년 10월 26일

Morpholine → N-(5-Methyl-1H-pyrazol-3-yl)-2-(methylthio)-6-morpholin-4-yl-5-nitropyrimidin-4-amine

https://huagongshe.com/reaction/450392

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물DiisopropylethylamineHCID 81531—
반응물1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
반응물4,6-Dichloro-2-(methylthio)-5-nitropyrimidineHCID 11345458—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물N-(5-Methyl-1H-pyrazol-3-yl)-2-(methylthio)-6-morpholin-4-yl-5-nitropyrimidin-4-amineHCID 68734536—

반응 단계

To a solution of 4,6-dichloro-2-(methylthio)-5-nitropyrimidine (Intermediate 56, 820 mg) in THF at 0° C. were added 5-methyl-1H-pyrazol-3-amine (350 mg) and DIPEA (1.6 ml) drop-wise. The resulting mixture was stirred at this temperature for 3 hours whereupon morpholine (1 ml) was added. The resulting mixture was allowed to warm to ambient temperature over 10 hours. The mixture was diluted with H2O and EtOAc and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, saturated NaHCO3 (aq) solution, dried and evaporation of the volatiles under reduced pressure gave a colored residue. Purification by column chromatography (50% EtOAc/hexanes) gave the title compound (820 mg). LCMS: 352 [M+1].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486966B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-0e93f9d296b14d52880e09c304f1e6b5
출처 메모uspto-grants-2013_07