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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42197Generated: October 30, 2026

Acetone → 2-{6-[4-(4-Benzyl-phthalazin-1-yl)-piperazin-1-yl]-pyridin-3-yl}-propane-1,2-diol

https://huagongshe.com/reaction/42197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantSodium SulfiteHCID 24437—
ReactantMethyl morpholine oxideHCID 82029—
ReactantHCID 44186377HCID 44186377—
CatalystPotassium osmate(VI) dihydrateHCID 53393272—
Solventtert-ButanolHCID 6386—
Product2-{6-[4-(4-Benzyl-phthalazin-1-yl)-piperazin-1-yl]-pyridin-3-yl}-propane-1,2-diolHCID 4418637872%

Reaction Steps

To 1-benzyl-4-[4-(5-isopropenyl-pyridin-2-yl)-piperazin-1-yl]-phthalazine (68 mg, 0.158 mmol) is added acetone (1 mL), t-butanol (0.5 mL), and H2O (0.5 mL). To this suspension is then added potassium osmate (VI) dihydrate (536 μg, 1.58 μM), and NMO (21 mg, 0.174 mmol), and the reaction is stirred at room temperature for 3 h. Sodium sulfite (350 mg) is added to the resulting clear orange solution and the mixture is stirred for 1 h. Additional H2O (25 mL) is added, and the organics extracted with EtOAc (3×25 mL), dried over MgSO4, and concentrated. Purification by flash chromatography on silica gel (90:10 CH2Cl2:MeOH) afforded a clear oil which was then triturated with EtOAc to afford the title compound as a white powder (52 mg, 72% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536168B2
Source datasetuspto-grants-2013_09
ORD IDord-009f8c573ce6455c8b254aa7822ef177
Source noteuspto-grants-2013_09