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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846229Generated: November 1, 2026

Dimethyl Sulfide → HCID 89964578, compound

https://huagongshe.com/reaction/1846229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 89964241HCID 89964241—
ReactantHCID 89964768HCID 89964768—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductHCID 89964578HCID 89964578—

Reaction Conditions

Temperature-78 °C

Reaction Steps

tert-butyl 4-oxo-3,4-dihydro-1,5-naphthyridine-1(2H)-carboxylate. To a solution of 9-methylene-6,7,8,9-tetrahydrooxepino[3,2-b]pyridine (1 eq.) in a mixture of solvents (MeOH:CHCl3) is added a catalytic amount of NaHCO3. The reaction mixture is cooled to −78° C. and purged with O3. Reaction progress is monitored by TLC. After the reaction is judged complete, the reaction mixture is quenched with dimethyl sulfide (5 eq.) at −78° C. The resulting mixture is stirred for 12 h at ambient temperature. The reaction mixture is diluted with EtOAc and water. The organic layer is washed with water, dried over Na2SO4, and concentrated in vacuo. The compound that may be thus obtained is purified by column chromatography to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952009B2
Source datasetuspto-grants-2015_02
ORD IDord-73ae112563af42bf9a1cfb4e00886e66
Source noteuspto-grants-2015_02