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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583395Generated: October 31, 2026

Potassium Iodide → 2-Isopropyl-11-oxo-11H-pyrido[2,1-b]quinazoline-8-carboxylic acid 4-pyridin-3-yl-butyl ester

https://huagongshe.com/reaction/1583395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12562128HCID 12562128—
Reactant4-(3-Pyridinyl)butyl chlorideHCID 13999760—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Isopropyl-11-oxo-11H-pyrido[2,1-b]quinazoline-8-carboxylic acid 4-pyridin-3-yl-butyl esterHCID 1355751344.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 0.70 g of 2-(1-methylethyl)-11-oxo-11H-pyrido[2,1-b]quinazoline-8-carboxylic acid, 0.50 g of 4-(3-pyridinyl)butylchloride, 0.40 g of potassium iodide and 0.39 g of potassium carbonate in 12 ml of dimethylformamide was stirred over night at a bath temperature of 50° C. The reaction mixture was diluted with ethylacetate, washed with water, dried (potassium carbonate) and concentrated. The residue was chromatographed on 75 g of silica gel eluting with ethyl acetate to give 0.46 g of a yellow solid which was recrystallized from ethyl acetate-hexane to give 0.33 g (32%), mp 95°-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551460
Source datasetuspto-grants-1985_11
ORD IDord-e442beb8ab094892863502f88436e092
Source noteuspto-grants-1985_11