Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077907Generated: October 25, 2026

Diisopropylethylamine → (R)-ethyl 4-(4-((6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzoate

https://huagongshe.com/reaction/2077907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 4-(piperazin-1-yl)benzoateHCID 2761178—
Reactant(Cyanomethyl)trimethylphosphanium iodideHCID 10514344—
Reactant(R)-3-(hydroxymethyl)-6a,7,9,10-tetrahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazin-6(5H)-oneHCID 58324367—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventPropionitrileHCID 7854—
Product(R)-ethyl 4-(4-((6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazin-3-yl)methyl)piperazin-1-yl)benzoateHCID 5832446782%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of (R)-3-(hydroxymethyl)-6a,7,9,10-tetrahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazin-6(5H)-one (333 mg, 1.325 mmol) in propiononitrile (3313 μl) was added (cyanomethyl)trimethylphosphonium iodide (386 mg, 1.590 mmol) and DIPEA (694 μl, 3.98 mmol) and finally ethyl 4-(piperazin-1-yl)benzoate (310 mg, 1.325 mmol). The vial was heated to 90° C. for 12 hours. The reaction was then cooled to room temperature, diluted with EtOH (8 ml) and water (1 mL), then filtered. The precipitate was filtered off and dried in vacuum to afford the title compound 508 mg, 82%) as a white solid. [M+H] calc'd for C24H29N5O3S, 468; found, 468.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928105B2
Source datasetuspto-grants-2011_04
ORD IDord-9cc64e6df75349c8a9c0cfbc6e377608
Source noteuspto-grants-2011_04