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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172071Generated: October 30, 2026

Triethylamine → Ethyl 2-((2-amino-5-bromopyridin-3-yl)methylamino)acetate

https://huagongshe.com/reaction/2172071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Reactant5-Bromo-3-(bromomethyl)pyridin-2-amine hydrobromideHCID 53420052—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-((2-amino-5-bromopyridin-3-yl)methylamino)acetateHCID 59456921—

Reaction Steps

Glycine ethyl ester hydrochloride (805 mg, 5.7 mmol) and triethylamine (2.6 mL, 18.46 mmol) were successively added to a solution of 5-bromo-3-(bromomethyl)pyridin-2-amine hydrobromide (2, 5.7 mmol) in dimethylformamide (65 mL) at room temperature. The reaction mixture was stirred overnight then partitioned between ethyl acetate (70 ml) and water (100 mL). The aqueous phase was separated and extracted with ethyl acetate (2×50 mL). The combined organic phases were washed with a saturated solution of sodium chloride (3×40 mL), dried over sodium sulfate, filtered and concentrated to dryness. The residue was purified by chromatography on silica gel, using dichloromethane/methanol (10:0 to 95:5) as eluent. The title product was obtained as a yellow solid (1.1 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051321B2
Source datasetuspto-grants-2015_06
ORD IDord-ff93910ff39f4ebaaeb67b323e8e16b7
Source noteuspto-grants-2015_06