HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83015Generated: October 25, 2026
Triethylamine → Ethyl 2-((2-amino-5-bromopyridin-3-yl)methylamino)acetate
https://huagongshe.com/reaction/83015
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| Reactant | 5-Bromo-3-(bromomethyl)pyridin-2-amine hydrobromide | HCID 53420052 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-((2-amino-5-bromopyridin-3-yl)methylamino)acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846711B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-8af2f4265a024dfe91b0b2dbcf96388c |
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| Source note | uspto-grants-2014_09 |
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