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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470011Generated: November 2, 2026

Triethylamine → N-(5-bromo-1,3-thiazol-2-yl)adamantane-1-carboxamide

https://huagongshe.com/reaction/1470011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Thiazolamine, 5-bromo-HCID 43600—
Reactant1-Adamantanecarbonyl chlorideHCID 98915—
SolventTetrahydrofuranHCID 8028—
ProductN-(5-bromo-1,3-thiazol-2-yl)adamantane-1-carboxamideHCID 49760640—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-bromothiazol-2-amine (3.0 g, 11.5 mmol), adamantane-1-carbonyl chloride (2.74 g, 13.8 mmol), triethylamine (3.2 mL, 23 mmol) and 4-di(methylamino)pyridine (1.1 g) in tetrahydrofuran (100 mL) was heated at 80° C. for 48 hours. The mixture was cooled to ambient temperature, concentrated, diluted with water and extracted with ethyl acetate. The organic extract was dried (Na2SO4), filtered and concentrated. Purification by flash chromatography (silica gel, 25% ethyl acetate/hexanes) afforded the title compound. MS (ESI) m/z 342 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006275B2
Source datasetuspto-grants-2015_04
ORD IDord-2a0c58798f664b1689cb0be26780835c
Source noteuspto-grants-2015_04