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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365959Generated: November 1, 2026

Triethylamine → N-(5-Fluoropyridin-2-yl)pivalamide

https://huagongshe.com/reaction/1365959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(5-Fluoropyridin-2-yl)pivalamideHCID 2229323776.6%

Reaction Steps

To a 0° C. solution of 2-amino-5-fluoropyridine (1.00 g, 8.92 mmol) and triethylamine (1.35 g, 13.4 mmol) in dichloromethane (30 mL) was added trimethylacetyl chloride (1.29 g, 10.7 mmol) and DMAP (0.11 g, 0.89 mmol). The solution was allowed to warm to room temperature. After 4 h, saturated aqueous NaHCO3 was added, the layers separated and the aqueous phase backwashed with DCM. The combined organics were dried over magnesium sulfate, filtered and concentrated and the residue purified by silica gel chromatography (5%→40% EtOAc/hexanes) to give the title compound (1.34 g). MS 197.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893052B2
Source datasetuspto-grants-2011_02
ORD IDord-6e2a5999aa4b4b9d8a614a804c64baca
Source noteuspto-grants-2011_02