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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097650생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1097650

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-[3-(Phenylmethyl)-1,2,4-oxadiazol-5-yl]-1-propanolHCID 59395573—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물8-Chloro-3-pentyl-1-(3-[3-(phenylmethyl)-1,2,4-oxadiazol-5-yl]propyl)-3,7-dihydro-1H-purine-2,6-dioneHCID 59395788—

반응 단계

A solution of 3-[3-(phenylmethyl)-1,2,4-oxadiazol-5-yl]-1-propanol (88 mg, 0.4 mmol) in THF (4 ml) was treated with 8-chloro-3-pentyl-7-(2-propen-1-yl)-3,7-dihydro-1H-purine-2,6-dione (100 mg, 0.34 mmol) and PPh3 (115 mg, 0.44 mmol) under nitrogen. DBAD (101 mg, 0.44 mmol) was added in one portion and the reaction left to react for 5 h. The mixture was degassed by applying a vacuum and then nitrogen was introduced. Pd(PPh3)4 (39 mg, 0.034 mmol) was added and the mixture degassed once more. Morpholine (294 μl, 3.4 mmol) was added and the mixture was stirred under nitrogen for 3 h. The mixture was partitioned between 2M HCl (aq) and EtOAc. The organic layer was separated, washed with brine, dried (MgSO4) and concentrated. The title compound was obtained as a white solid after purification by MDAP (64 mg, 42%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143264B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-b15438e57bd24b7aaab077db1851457d
출처 메모uspto-grants-2012_03