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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472162Generated: October 25, 2026

Pivaloyl chloride → N-(5-Bromo-pyridin-3-yl)-2,2-dimethyl-propionamide

https://huagongshe.com/reaction/1472162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
Reactant3-Amino-5-bromopyridineHCID 817681—
SolventPyridineHCID 1049—
ProductN-(5-Bromo-pyridin-3-yl)-2,2-dimethyl-propionamideHCID 2422918973.1%

Reaction Steps

To a solution of 3-amino-5-bromo pyridine (XXV) (1.0 g, 5.78 mmol) in dry pyridine (10 mL) was added pivaloyl chloride (XXVIII) (769 mg, 6.38 mmol). The reaction mixture was stirred at room temperature for 3 h. The reaction was poured into an ice water/saturated aqueous NaHCO3 mixture and stirred for 30 min. The precipitate was filtered, washed with cold water and dried at room temperature to yield N-(5-bromopyridin-3-yl)pivalamide (XXIX) as an off-white solid (1.082 g, 4.22 mmol, 73.1% yield). 1H NMR (DMSO-d6, 500 MHz) δ ppm 1.23 (s, 9H), 8.37 (d, J=2 Hz, 1H), 8.39 (t, J=2 Hz, 1H), 8.80 (d, J=2 Hz, 1H), 9.58 (brs, 1H); ESIMS found C10H13BrN2O m/z 257.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012472B2
Source datasetuspto-grants-2015_04
ORD IDord-55b3668c4f3a42b8aa24f79d55820109
Source noteuspto-grants-2015_04