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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406202Generated: October 30, 2026

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

https://huagongshe.com/reaction/406202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptanoic acid, 7-oxo-, ethyl esterHCID 77609—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(R)-2,3-diphenyl-5,6,7,8-tetrahydropyrido[2,3-b]pyrazin-8-yl acetateHCID 66665795—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product(R)-Ethyl 7-(8-acetoxy-2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)heptanoateHCID 86681847—

Reaction Steps

To a solution of (R)-2,3-diphenyl-5,6,7,8-tetrahydropyrido[2,3-b]pyrazin-8-yl acetate (Intermediate HBR) in DCE (7 ml) was added ethyl 7-oxoheptanoate (71.8 mg, 0.417 mmol) followed by sodium triacetoxyborohydride (236 mg, 1.112 mmol). The reaction mixture was left to stir at room temperature overnight under an atmosphere of nitrogen. A further portion of ethyl 7-oxoheptanoate (6 equivalents) was added and the reaction mixture was left to stir at RT for 4 days. The mixture was diluted with water (20 ml) and extracted with EtOAc (3×20 ml). The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo. The resulting crude product was purified by chromatography on silica eluting with 0-40% EtOAc/iso-hexane to afford the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754085B2
Source datasetuspto-grants-2014_06
ORD IDord-f98ae746e42e4543bf61b3e9b0a3ece2
Source noteuspto-grants-2014_06