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HRID 1097650作成日:2026年10月27日

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

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-[3-(Phenylmethyl)-1,2,4-oxadiazol-5-yl]-1-propanolHCID 59395573—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物8-Chloro-3-pentyl-1-(3-[3-(phenylmethyl)-1,2,4-oxadiazol-5-yl]propyl)-3,7-dihydro-1H-purine-2,6-dioneHCID 59395788—

反応手順

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%).

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-b15438e57bd24b7aaab077db1851457d
出典メモuspto-grants-2012_03