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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175798Generated: October 31, 2026

Triethylamine → HCID 23153909, compound

https://huagongshe.com/reaction/1175798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23154093HCID 23154093—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23153909HCID 23153909—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-{2-[4-(2-hydroxyethyl)phenyl]-5-(4-methoxybenzyl)-4-oxo-4,5-dihydro-2H-pyrazolo[4,3-c]quinolin-3-yl}acetamide (0.2 g) and triethylamine (0.12 ml) in tetrahydrofuran (25 ml) was added dropwise methanesulfonyl chloride (0.048 ml) at 0° C. The solution was stirred at 0° C. for 2 hours and at room temperature for 15 minutes, an aqueous sodium hydrogen carbonate solution was added thereto, and extracted with ethyl acetate. The extract was washed with water and saturated brine, dried and concentrated under reduced pressure. To the residue was added ethanol (30 ml), triethylamine (0.087 ml), piperidine (0.045 ml) and the mixture was refluxed with heating. After 2 hours, piperidine (0.1 ml) was added thereto, and the mixture was stirred with heating for 6 hours. The solvent was distilled off under reduced pressure, ethyl acetate was added thereto, and extracted with 1N hydrochloric acid. The aqueous layer was washed ether, basified by adding a 2N aqueous sodium hydroxide solution, and extracted with ethyl acetate. The extract was washed with saturated brine, dried and concentrated under reduced pressure to obtain the target compound (0.13 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842701B2
Source datasetuspto-grants-2010_11
ORD IDord-af19d5c5cb5b42c5ad5d125c7600a143
Source noteuspto-grants-2010_11