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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716286Generated: October 25, 2026

Potassium Carbonate → (R)-methyl 6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazine-3-carboxylate

https://huagongshe.com/reaction/716286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 6-chloro-5-nitronicotinateHCID 346961—
Reactant(R)-thiomorpholine-3-carboxylic acidHCID 1152541—
CatalystTriphenyl phosphiteHCID 7540—
CatalystPlatinumHCID 23939—
CatalystAmmonium metavanadateHCID 516859—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(R)-methyl 6-oxo-5,6,6a,7,9,10-hexahydropyrido[3,2-e][1,4]thiazino[4,3-a]pyrazine-3-carboxylateHCID 5832449752%

Reaction Steps

To a suspension of (R)-thiomorpholine-3-carboxylic acid (1.009 g, 6.86 mmol) in THF was added methyl 6-chloro-5-nitronicotinate (1.35 g, 6.23 mmol) and potassium carbonate (2.58 g, 18.70 mmol). The suspension was heated to reflux for 3 hours. The crude orange solution was allowed to cool to RT and filtered through a pad of celite which was washed with DCM (50 mL), and transferred to a bomb hydroginator. To the solution was added triphenyl phosphite (0.019 ml, 0.061 mmol), platinum (0.238 g, 0.061 mmol), and ammonium metavanadate. The vessel was sealed and pressurized to 140 psi with stirring for 24 h at room temperature. The vessel was depressurized and the mixture was diluted with DCM (100 mL) and refluxed for 30 minutes. The hot mixture was filtered through celite and concentrated to yield 887 mg (52%) of the product as a white solid. [M+H] calc'd for C12H13N3O3S, 280. found, 280.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187497B2
Source datasetuspto-grants-2015_11
ORD IDord-eb89dc9f30d647d89719a86b7d1407c4
Source noteuspto-grants-2015_11