Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504675Generated: October 31, 2026

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

https://huagongshe.com/reaction/1504675

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 numberUS09215870B2
Source datasetuspto-grants-2015_12
ORD IDord-4db287bdbb7b4af7b686a89a30f05105
Source noteuspto-grants-2015_12