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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097650Generated: October 25, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriphenylphosphineHCID 11776—
ReactantDibenzyl azodicarboxylateHCID 5387121—
Reactant7-Allyl-8-chloro-3-pentyl-1H-purine-2,6(3H,7H)-dioneHCID 59299557—
Reactant3-[3-(Phenylmethyl)-1,2,4-oxadiazol-5-yl]-1-propanolHCID 59395573—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product8-Chloro-3-pentyl-1-(3-[3-(phenylmethyl)-1,2,4-oxadiazol-5-yl]propyl)-3,7-dihydro-1H-purine-2,6-dioneHCID 59395788—

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143264B2
Source datasetuspto-grants-2012_03
ORD IDord-b15438e57bd24b7aaab077db1851457d
Source noteuspto-grants-2012_03