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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097727생성일: 2026년 10월 27일

Morpholine → 8-Chloro-1-{4-[2-oxo-1-(phenylmethyl)-3-pyrrolidinyl]butyl}-3-pentyl-3,7-dihydro-1H-purine-2,6-dione

https://huagongshe.com/reaction/1097727

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물Potassium CarbonateHCID 11430—
반응물7-Allyl-8-chloro-3-pentyl-1H-purine-2,6(3H,7H)-dioneHCID 59299557—
반응물3-(4-Bromobutyl)-1-(phenylmethyl)-2-pyrrolidinoneHCID 59395857—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물8-Chloro-1-{4-[2-oxo-1-(phenylmethyl)-3-pyrrolidinyl]butyl}-3-pentyl-3,7-dihydro-1H-purine-2,6-dioneHCID 59395855—

반응 조건

온도50 °C

반응 단계

To a solution of 8-chloro-3-pentyl-7-(2-propen-1-yl)-3,7-dihydro-1H-purine-2,6-dione (0.086 g, 0.29 mmol) and 3-(4-bromobutyl)-1-(phenylmethyl)-2-pyrrolidinone (0.17 g, 0.55 mmol, 1:1 mixture with 2-(phenylmethyl)-2-azaspiro[4.4]nonan-1-one) in THF (5 ml) was added potassium carbonate (0.08 g, 0.58 mmol) and the mixture heated and stirred at 50° C. for 18 h. The solution was allowed to cool then degassed (sequential evacuation followed by addition of nitrogen×3) and Pd(PPh3)4 (0.09 g, 0.077 mmol) followed by morpholine (0.2 ml, 2.2 mmol) added and the solution stirred at ambient temperature for 18 h. The solution was separated between ethyl acetate and dil HCl and the organics washed with brine, dried and concentrated. Purification of the residues using an aminopropyl SPE (5 g) eluting first with MeOH then 5% AcOH/MeOH yielded the title compound as a yellow oil which crystallised on standing under ether (0.031 g, 22%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143264B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-575039136bbd40398a94ce0be4c619b7
출처 메모uspto-grants-2012_03