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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469957Generated: October 26, 2026

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

https://huagongshe.com/reaction/1469957

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 numberUS09006275B2
Source datasetuspto-grants-2015_04
ORD IDord-bda2508b03034f0f9d6e0795045818d3
Source noteuspto-grants-2015_04