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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097751Generated: October 26, 2026

Carbon Tetrachloride → 3-Benzyloxy-7-methyl-2-(5-m-tolyl-[1,3,4]oxadiazol-2-yl)-pyrido[1,2-a]pyrimidin-4-one

https://huagongshe.com/reaction/1097751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Methyl-benzoic acid N'-(3-benzyloxy-7-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidine-2-carbonyl)-hydrazideHCID 59392915—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product3-Benzyloxy-7-methyl-2-(5-m-tolyl-[1,3,4]oxadiazol-2-yl)-pyrido[1,2-a]pyrimidin-4-oneHCID 58101033—

Reaction Steps

The product from Example 8.3 (202 mg, 0.457 mmol), carbon tetrachloride (0.221 mL, 2.28 mmol) and triethylamine (0.165 mL, 1.19 mmol) were mixed with acetonitrile (10 mL). To this mixture was added triphenylphosphine (291 mg, 1.11 mmol) at room temperature. After being stirred at room temperature overnight, the reaction solution was diluted with ethyl acetate (100 mL), washed with aqueous saturated sodium bicarbonate (50 mL), water (50 mL) and brine (50 mL) successively, and then dried (Na2SO4). The crude product was subjected to flash chromatography (hexane-ethyl acetate 1:1) to give the desired compound

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143268B2
Source datasetuspto-grants-2012_03
ORD IDord-0808d578dfd24024b99b0b7f76012547
Source noteuspto-grants-2012_03