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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385032Generated: November 1, 2026

Triethylamine → HCID 178425694, compound

https://huagongshe.com/reaction/1385032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant8-Methylquinoline-5-carbonyl chlorideHCID 21184122—
ReactantHCID 178481816HCID 178481816—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 178425694HCID 178425694—

Reaction Steps

At 0° C., 1.70 g of 8-methylquinoline-5-carbonyl chloride were added to 0.81 g of 5-hydroxy-1-methylpyrazole and 0.92 g of triethylamine in 30 ml of acetonitrile. The reaction mixture was stirred for 3 hours at room temperature and then taken up in ethyl acetate and washed with aqueous sodium carbonate solution, and the organic phase was then dried and concentrated. The residue was treated with 10 ml of dioxane and 1.71 g of dry potassium carbonate and heated under reflux for 14 hours. After cooling, water was added and the aqueous phase was washed with ethyl acetate and acidified with 2N hydrochloric acid. The precipitate was filtered off under suction and the acidified aqueous phase was extracted with ethyl acetate. This organic phase was dried and concentrated. The residue and the precipitate were combined.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262074B1
Source datasetuspto-grants-2001_07
ORD IDord-43d12c26b9c84cedbcc07d16a08d1be7
Source noteuspto-grants-2001_07