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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664770Generated: October 26, 2026

2-Amino-3-bromopyridine → Benzyl 4-[2-[(3-bromopyridin-2-yl)amino]-2-oxoethyl}-3,6-dihydropyridine-1(2H)-carboxylate

https://huagongshe.com/reaction/1664770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-bromopyridineHCID 817700—
ReactantTrimethylaluminumHCID 16682925—
ReactantBenzyl 4-(2-methoxy-2-oxoethyl)-3,6-dihydropyridine-1(2H)-carboxylateHCID 59555173—
Solvent1,2-DichloroethaneHCID 11—
ProductBenzyl 4-[2-[(3-bromopyridin-2-yl)amino]-2-oxoethyl}-3,6-dihydropyridine-1(2H)-carboxylateHCID 59555280189%

Reaction Conditions

Temperature55 °C

Reaction Steps

Trimethylaluminum (2.0 M, 2.05 mL, 4.10 mol) was added slowly to a 0° C. solution of benzyl 4-(2-methoxy-2-oxoethyl)-3,6-dihydropyridine-1(2H)-carboxylate (0.79 g, 2.73 mol) and 2-amino-3-bromopyridine (0.520 g, 3.00 mmol) in 1,2-dichloroethane (15 mL). After 30 min, the reaction was heated to 55° C. for 48 h. The reaction was quenched by the careful addition of saturated aqueous sodium bicarbonate and the mixture extracted with dichlormethane (4×). The combined organic layers were washed with 1N sodium potassium tartrate, brine, dried over MgSO4, filtered, and concentrated. The crude product was purified by silica gel chromatography, eluting with a gradient of 50 to 100% ethyl acetate:hexanes to give the title compound (2.44 g). MS: m/z=430.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039460B2
Source datasetuspto-grants-2011_10
ORD IDord-171773d38afd4bd4adcce76cbeab4beb
Source noteuspto-grants-2011_10