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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255852Generated: October 30, 2026

Carbon Dioxide → n-Propyl Cinnoline-4-carboxylate

https://huagongshe.com/reaction/255852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantCinnoline-4-carboxylic acidHCID 89099—
ReactantImidazole sodiumHCID 57373095—
SolventTetrahydrofuranHCID 8028—
Productn-Propyl Cinnoline-4-carboxylateHCID 20164604—

Reaction Steps

A suspension of 870 mg of 1, and 850 mg of carbonyidimidazole (CDII) in 30 ml of tetrahydrofuran (THF) was stirred at room temperature until CO2 evolution ceased (ca. 30 minutes). After being stirred for 2 hours, the resulting mixture was treated with 320 mg of dry nypropanol and 3 drops of a 0.1 M solution of sodium imidazole in THE. The mixture was held at room temperature overnight, then the solvent was evaporated and the residue was partitioned between water and ether. The etheral extract was washed with saturated sodium bicarbonate solution, then with brine, then dried (MgSO4) and stripped in a rotary evaporator. The residue was chromatographed over silica gel, using a 1:1 v:v mixture of cyclohexane and ethyl acetate as eluent, to give 5, as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699651
Source datasetuspto-grants-1987_10
ORD IDord-e63f5621c93e4a72858163153f30ce58
Source noteuspto-grants-1987_10