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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255076Generated: October 25, 2026

Triethylamine → Adamantane-1-carboxylic acid (5-chloro-thiazol-2-yl)-amide

https://huagongshe.com/reaction/255076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-5-chlorothiazoleHCID 38942—
Reactant1-Adamantanecarbonyl chlorideHCID 98915—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductAdamantane-1-carboxylic acid (5-chloro-thiazol-2-yl)-amideHCID 8661904851.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-amino-5-chlorothiazole (2.00 g, 14.9 mmol), 1-adamantanecarbonyl chloride (3.54 g, 17.8 mmol), 4-dimethylaminopyridine (1.10 g, 0.90 mmol) and triethylamine (4.15 mL, 23.0 mmol) in 80 mL of THF was stirred at 80° C. for 48 hours The mixture was cooled to ambient temperature, diluted with 100 mL of ethyl acetate and washed with brine. The layers were separated and the aqueous phase was extracted twice with 50 mL of ethyl acetate. The combined organic extracts were dried over anhydrous Na2SO4, filtered, and concentrated. Purification by column chromatography (SiO2, dichloromethane) afforded 2.27 g of the title compound: MS (DCI/NH3) m/z 297 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875639B2
Source datasetuspto-grants-2011_01
ORD IDord-db9f264b210b4ee888b9dfde0a1eb5e9
Source noteuspto-grants-2011_01