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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517898Generated: October 30, 2026

Sodium triacetoxyborohydride → Ethyl 6-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)hexanoate

https://huagongshe.com/reaction/517898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl 6-oxohexanoateHCID 11171124—
Reactant2,3-Di-p-tolyl-5,6,7,8-tetrahydropyrido[2,3-b]pyrazineHCID 66664525—
Solvent1,2-DichloroethaneHCID 11—
ProductEthyl 6-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)hexanoateHCID 89689920—

Reaction Steps

A solution of 2,3-di-p-tolyl-5,6,7,8-tetrahydropyrido[2,3-b]pyrazine (Intermediate B) (2.0 g, 6.34 mmol) and ethyl 6-oxohexanoate (Intermediate A) (2.508 g, 12.68 mmol) in 1,2-dichloroethane (50 ml) was treated with sodium triacetoxyborohydride (3.36 g, 15.85 mmol) and the resultant suspension was stirred at room temperature overnight. The solution was treated with sat.NaHCO3 and extracted with DCM (×3). The organic extracts were dried (MgSO4) and evaporated under reduced pressure. The residue was loaded onto an Isolute® SCX-2 cartridge and eluted with MeOH followed by 2M NH3 in MeOH. The methanolic ammonia fractions were concentrated under reduced pressure and further purified by chromatography on silica eluting with 10-50% EtOAc in iso-hexane to afford the titled compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115129B2
Source datasetuspto-grants-2015_08
ORD IDord-260e12903989443985adf15e1d2488c0
Source noteuspto-grants-2015_08