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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672574Generated: October 31, 2026

Potassium Carbonate → 5-(5-Bromopyridin-2-yl)-4-ethyloxazole

https://huagongshe.com/reaction/1672574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromopyridine-2-carbaldehydeHCID 9877562—
Reactant1-Ethyl-1-tosylmethyl isocyanideHCID 20467189—
SolventMethanolHCID 887—
Product5-(5-Bromopyridin-2-yl)-4-ethyloxazoleHCID 6669659688%

Reaction Steps

A mixture of 1-(1-isocyanopropylsulfonyl)-4-methylbenzene (1.98 g, 8.87 mmol), 5-bromopicolinaldehyde (1.65 g, 8.87 mmol), and K2CO3 (1.47 g, 10.6 mmol) in MeOH (45 mL) was heated at reflux overnight. The reaction was cooled to ambient temperature and concentrated in vacuo. Water was added to the residue and the product was extracted with EtOAc. The combined organic extract was washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo. The crude product was chromatographed on silica gel (Analogix® 25×60 column, 10%-50% EtOAc/hexanes) to yield 1.97 g (88%) of the title compound. 1H NMR (300 MHz, CDCl3) δ 8.68 (dd, J=2.4, 0.5, 1H), 7.89-7.82 (m, 2H), 7.55-7.49 (m, 1H), 3.06 (q, J=7.5, 2H), 1.29 (t, J=7.5, 3H). MS (DCI+) m/z 253/255 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998993B2
Source datasetuspto-grants-2011_08
ORD IDord-ee852080ca7f4a08b4c52efa68c8e990
Source noteuspto-grants-2011_08