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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097676생성일: 2026년 10월 26일

Morpholine → 8-Chloro-3-pentyl-1-{3-[5-(phenylmethyl)-1,2,4-oxadiazol-3-yl]propyl}-3,7-dihydro-1H-purine-2,6-dione

https://huagongshe.com/reaction/1097676

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물TriphenylphosphineHCID 11776—
반응물Dibenzyl azodicarboxylateHCID 5387121—
반응물7-Allyl-8-chloro-3-pentyl-1H-purine-2,6(3H,7H)-dioneHCID 59299557—
반응물3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]-1-propanolHCID 59395802—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물8-Chloro-3-pentyl-1-{3-[5-(phenylmethyl)-1,2,4-oxadiazol-3-yl]propyl}-3,7-dihydro-1H-purine-2,6-dioneHCID 5939552720%

반응 단계

To a stirred solution of 8-chloro-3-pentyl-7-(2-propen-1-yl)-3,7-dihydro-1H-purine-2,6-dione (0.20, 0.67 mmol) in THF (5 ml) was added 3-[5-(phenylmethyl)-1,2,4-oxadiazol-3-yl]-1-propanol (0.162 g, 0.74 mmol), DBAD (0.186 g, 0.81 mmol) and triphenylphosphine (0.212 g, 0.81 mmol) and the solution stirred for 18 h. To the solution was added Pd(PPh3)4 (75 mg, 0.067 mmol) and morpholine (604 μl, 6.7 mmol) were added and stirred for at rt under nitrogen for a further 3 h. 75 mg of Pd(PPh3)4 was added and the mixture left to stir for another 3 h. The mixture was partitioned between EtOAc and 2M HCl (aq). The organic layer was separated, washed with brine, dried (MgSO4) and concentrated. The crude material was purified by an aminopropyl SPE using MeOH to load the compound onto the column and wash through the impurities, then with 2-4% AcOH/MeOH to elute the compound. The product fractions were combined and concentrated then further purified by MDAP. The product fractions were combined and concentrated give the title compound as a white solid (51 mg, 20%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143264B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-51fe2b08ba1a4a6fa16b6c7ca620c5e2
출처 메모uspto-grants-2012_03