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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633970Generated: October 27, 2026

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

https://huagongshe.com/reaction/633970

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 numberUS09321769B2
Source datasetuspto-grants-2016_04
ORD IDord-0cdd2ae8b0b24eb0bbc106c534b19b6b
Source noteuspto-grants-2016_04