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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503722Generated: October 30, 2026

Sodium hydride → Ethyl 2-amino-2-(5-bromo-3-chloropyridin-2-yl)acetate

https://huagongshe.com/reaction/1503722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
Reactant5-Bromo-2,3-dichloropyridineHCID 12747760—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-amino-2-(5-bromo-3-chloropyridin-2-yl)acetateHCID 7113850320%

Reaction Steps

Ethyl 2-(diphenylmethyleneamino)acetate (10.2 g, 38.2 mmol) was added to sodium hydride (NaH; 3.18 g, 133.52 mmol) in DMF (50 mL) at 0° C., and the mixture was stirred for 30 min. To this was added 5-bromo-2,3-dichloropyridine (12.9 g, 57.23 mmol), and the reaction mixture was stirred for 3 h at ambient temperature. The reaction mixture was quenched with 2 N HCl solution and then stirred for 4 h at ambient temperature. The mixture was extracted with EtOAc. The combined EtOAc layer was washed with brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure. Purification by flash column chromatography (20-30% EtOAc in hexane) afforded the title compound as a liquid (1.3 g, 20%): 1H NMR (400 MHz, CDCl3) δ 8.52 (s, 1H), 7.89 (s, 1H), 5.09 (s1H), 4.23 (m, 2H), 2.27 (br s, 2H), 1.26 (m, 3H); ESIMS m/z 293.05 ([M+H]+); IR (thin film) 3381, 3306, 1742, 759, 523 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212164B2
Source datasetuspto-grants-2015_12
ORD IDord-e0790a077c4a46c087183e5f2bf74351
Source noteuspto-grants-2015_12