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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155050Generated: October 31, 2026

Triethylamine → HCID 178522547, compound

https://huagongshe.com/reaction/1155050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-AminooxazoleHCID 558521—
ReactantHCID 178521117HCID 178521117—
SolventEthyl AcetateHCID 8857—
ProductHCID 178522547HCID 17852254734.5%

Reaction Steps

A solution of 15.9 g of 2,8-bis-(trifluoromethyl)-4-hydroxy-3-quinoline-carboxylic acid chloride in 210 ml of ethyl acetate was added with stirring at 5°-8° C. under nitrogen to a solution of 3.57 g of 2-amino-oxazole and 4.3 g of triethylamine in 50 ml of ethyl acetate and after the temperature returned to room temperature, it stood overnight at that temperature. The mixture was vacuum filtered and the filtrate was washed and evaporated to dryness under reduced pressure. The 14.23 g of residue was triturated with 100 ml of N sodium hydroxide solution for 3 hours and was then diluted with 200 ml of water. The mixture was vacuum filtered and the filtrate was treated with activated carbon. The pH was adjusted to 1 by addition of N hydrochloric acid and the mixture was vacuum filtered. The recovered product was washed with water and dissolved in ethyl acetate. The solution was evaporated to dryness and the 8.77 g of product were crystallized twice from acetic acid to obtain 5.73 g (30.8% yield) of 2,8-bis-(trifluoromethyl)-4-hydroxy-N-(oxazol-2-yl)-3-quinoline-carboxamide melting at 258° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04299831
Source datasetuspto-grants-1981_11
ORD IDord-3da92b5fddf84909ace719a96126a6f9
Source noteuspto-grants-1981_11