Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40542Generated: October 26, 2026

Diisopropylethylamine → 2-methoxy-2-methyl-N-(5-phenylethynyl-pyridin-2-yl)-propionamide

https://huagongshe.com/reaction/40542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Bromo-1-ethylpyridinium tetrafluoroborateHCID 2736300—
Reactant2-methoxy-2-methylpropanoic acidHCID 9855465—
Reactant5-Phenylethynyl-pyridin-2-ylamineHCID 46854190—
SolventDichloromethaneHCID 6344—
Product2-methoxy-2-methyl-N-(5-phenylethynyl-pyridin-2-yl)-propionamideHCID 7154834246.2%

Reaction Steps

(100 mg, 0.515 mmol) 5-Phenylethynyl-pyridin-2-ylamine (Example 1, step 1) was dissolved in dichloromethane (5 ml) and 2-methoxy-2-methylpropionic acid (91 mg, 0.77 mmol, 1.5 equiv.), 2-bromo-1-ethyl pyridinium tetrafluoroborate (CAS 878-23-9) (211 mg, 0.77 mmol, 1.5 equiv.) and Hunig's Base (0.26 ml, 1.54 mmol, 3 equiv.) were added. The mixture was stirred for 14 hours at room temperature. The reaction mixture was extracted with saturated Na2CO3 solution and dichloromethane. The organic layer was dried over sodium sulfate and evaporated to dryness. The crude product was purified by prep HPLC to afford the desired 2-methoxy-2-methyl-N-(5-phenylethynyl-pyridin-2-yl)-propionamide (70 mg, 46% yield) was obtained as a yellow oil, MS: m/e=295.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530472B2
Source datasetuspto-grants-2013_09
ORD IDord-98a07b23b5e94b878356f0ee97fa61bd
Source noteuspto-grants-2013_09