Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362112Generated: November 1, 2026

Diisopropylethylamine → 3-[(2-Amino-5-bromo-pyridin-3-ylmethyl)amino]propionic acid ethyl ester

https://huagongshe.com/reaction/1362112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
Reactant5-Bromo-3-(bromomethyl)pyridin-2-amine hydrobromideHCID 53420052—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-[(2-Amino-5-bromo-pyridin-3-ylmethyl)amino]propionic acid ethyl esterHCID 5945696823.2%

Reaction Steps

A mixture of 5-bromo-3-bromomethyl-pyridin-2-ylamine hydrobromide (9.41 g, 27.1 mmol) and β-alanine ethyl ester hydrochloride (5.00 g, 32.5 mmol) in DMF (75 mL) was treated with N,N-diisopropylethylamine (16.5 mL, 94.9 mmol). After stirring at room temperature for 4 h, the cloudy mixture was diluted with CH2Cl2 (100 mL) and H2O. The aqueous layer was extracted with CH2Cl2 (2×150 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent removed in vacuo. Purification by column chromatography (silica gel, CH2Cl2/MeOH/Et3N, 95/4.5/0.5 to 80/19.5/0.5) gave the title compound (1.90 g, 23%) as a tan oil: MS (ESI) m/le 302 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-3020d719821f4c968e17bdf981249756
Source noteuspto-grants-2011_02