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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276535Generated: October 30, 2026

Heptanoic acid, 7-oxo-, ethyl ester → Ethyl 7-(2-phenyl-3-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoate

https://huagongshe.com/reaction/2276535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptanoic acid, 7-oxo-, ethyl esterHCID 77609—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Phenyl-3-p-tolyl-5,6,7,8-tetrahydropyrido[2,3-b]pyrazineHCID 66666256—
Solvent1,2-DichloroethaneHCID 11—
SolventSodium BicarbonateHCID 516892—
ProductEthyl 7-(2-phenyl-3-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoateHCID 66665828—

Reaction Steps

A solution of 2-phenyl-3-p-tolyl-5,6,7,8-tetrahydropyrido[2,3-b]pyrazine (Intermediate FA) (1.03 g, 3.42 mmol) in 1,2-dichloroethane (15 ml) was treated with ethyl 7-oxoheptanoate (1.776 g, 10.25 mmol) followed by sodium triacetoxyborohydride (3.62 g, 17.09 mmol). The reaction mixture was stirred at room temperature overnight. The mixture was diluted with saturated NaHCO3 (70 ml) and was extracted with DCM (×3). The combined organics were dried (MgSO4), filtered and concentrated in vacuo. The resulting crude product was purified by chromatography on silica eluting with 0-60% EtOAc/iso-hexane to give an oil. The product was loaded onto an Isolute™ SCX-2 cartridge, washed with MeOH and eluted with 2M NH3 in MeOH. The methanolic ammonia fractions were concentrated in vacuo to afford the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09132127B2
Source datasetuspto-grants-2015_09
ORD IDord-fbdccc89f71f4aa0a09ad869ebf31666
Source noteuspto-grants-2015_09