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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077826Generated: October 25, 2026

Diisopropylethylamine → (S)-ethyl 6-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)nicotinate

https://huagongshe.com/reaction/2077826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(Cyanomethyl)trimethylphosphanium iodideHCID 10514344—
ReactantEthyl 6-(piperazin-1-yl)nicotinateHCID 14987933—
Reactant(S)-3-(hydroxymethyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-oneHCID 58324378—
SolventWaterHCID 962—
SolventPropionitrileHCID 7854—
SolventPotassium CarbonateHCID 11430—
Product(S)-ethyl 6-(4-((6-oxo-5,6,6a,7,8,9-hexahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-3-yl)methyl)piperazin-1-yl)nicotinateHCID 4686460777%

Reaction Conditions

Temperature90 °C

Reaction Steps

(S)-3-(hydroxymethyl)-6a,7,8,9-tetrahydropyrido[3,2-e]pyrrolo[1,2-a]pyrazin-6(5H)-one (233 mg, 1.06 mmol), ethyl 6-(piperazin-1-yl)nicotinate (270 mg, 0.1.15 mmol), DIPEA (0.80 mL), and (cyanomethyl)trimethylphosphonium iodide (369 mg, 01.82 mmol) were suspended in propionitrile (3 mL) and heated in a closed vial at 90° C. for 5 h. The mixture was cooled, diluted with a solution of K2CO3 (2.50 g) in water (15 mL) and extracted with dichloromethane (2×10 mL). The combined organic extracts were dried (MgSO4) and concentrated in vacuo. The resulting oil was crystallized with ethyl ether-ethanol (10:1, 22 mL) to afford the title compounds as a tan solid (0.355 mg, 77%). [M+H] calc'd for C23H28N6O3, 437; found, 437.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928105B2
Source datasetuspto-grants-2011_04
ORD IDord-a88ef2b969934fa48330b09d8ebe7189
Source noteuspto-grants-2011_04