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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587715Generated: October 28, 2026

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

https://huagongshe.com/reaction/587715

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 (s 1H), 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 numberUS09226501B2
Source datasetuspto-grants-2016_01
ORD IDord-21bd44bb1ec148758c74aaee14b18e21
Source noteuspto-grants-2016_01