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HRID 1097676作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物TriphenylphosphineHCID 11776—
反応物Dibenzyl azodicarboxylateHCID 5387121—
反応物7-Allyl-8-chloro-3-pentyl-1H-purine-2,6(3H,7H)-dioneHCID 59299557—
反応物3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]-1-propanolHCID 59395802—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物8-Chloro-3-pentyl-1-{3-[5-(phenylmethyl)-1,2,4-oxadiazol-3-yl]propyl}-3,7-dihydro-1H-purine-2,6-dioneHCID 5939552720%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08143264B2
出典データセットuspto-grants-2012_03
ORD IDord-51fe2b08ba1a4a6fa16b6c7ca620c5e2
出典メモuspto-grants-2012_03