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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891272Generated: October 31, 2026

Triethylamine → HCID 64124842, compound

https://huagongshe.com/reaction/1891272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-Bromopyridine-2-carbaldehydeHCID 9877562—
SolventMethanolHCID 887—
ProductHCID 64124842HCID 6412484251.6%

Reaction Steps

Glycine ethyl ester hydrochloride (9C2) (161 mmol, 22.51 g) was dried under vacuum then dissolved in methanol (200 ml). Triethylamine (137 mmol, 13.87 g) was added with stirring and the resulting solution was added dropwise to a solution of 5-bromo-2-formylpyridine (9B1) (81 mmol, 15 g) in methanol (200 ml) under nitrogen. After 30 min, sodium triacetoxyborohydride (194 mmol, 41.0 g) was added portionwise over 30 min and the reaction was then stirred at room temperature under nitrogen overnight. The reaction was quenched with saturated sodium bicarbonate solution and extracted three times with DCM. The combined organic layers were washed with water, brine and dried using a hydrophobic frit, then concentrated under reduced pressure. The reside was purified on silica eluting with heptane/EtOAc/EtOH 8/1.6/0.4 to 5/4/1 to give ethyl 2-((5-bromopyridin-2-yl)methylamino)acetate (9J1) 11.4 g (51.6%); 1H NMR (400 MHz, CDCl3) 8.61 (s, 1H) 7.78 (d, 1H) 7.27 (d, 1H) 4.20 (q, 2H) 3.91 (s, 2H) 3.46 (s, 2H) 2.31 (bs, 1H) 1.27 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507521B2
Source datasetuspto-grants-2013_08
ORD IDord-711eea29b7c146019ed58da8a6770084
Source noteuspto-grants-2013_08