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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350963Generated: November 1, 2026

Triethylamine → HCID 21090614, compound

https://huagongshe.com/reaction/350963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzenamine, 4-(4-morpholinyl)-HCID 75655—
Reactant3-(Pyridin-2-yl)-2-sulfanylidene-1,3-thiazolidin-4-oneHCID 22345835—
CatalystMercuric ChlorideHCID 24085—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21090614HCID 2109061444.4%

Reaction Steps

3-(2-pyridyl)-2-thioxo-thiazolidin-4-one (1.1 g, 5.3 mmol, 1.0 equiv), prepared as described in J. Chem. Soc. (1956) 1644, was dissolved in 30 ml THF and charged with 4-morpholin-4-yl aniline (0.94 g, 5.28 mmol, 1.0 equiv) and Et3N (1.47 ml, 10.6 mmol, 2.0 equiv). Mercury (II) chloride (1.4 g, 5.28 mmol, 1.0 equiv) was added in one portion as a solid, and the heterogeneous mixture was stirred at ambient temperature overnight. The reaction mixture was filtered through Celite, and the filtrate was partitioned between EtOAc and saturated NH4Cl. The organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. Flash chromatography (40% to 100% EtOAc in hexanes, silica) afforded 0.83 g (44%) of the title compound: 1H NMR (300 MHz, CDCl3) δ 8.70 (m, 1H), 7.90 (m, 1H), 7.37–7.44 (m, 2H), 3.99 (s, 2H), 3.84 (m, 4H), 3.11 (m, 4H); MS (ESI) m/z=355.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183302B2
Source datasetuspto-grants-2007_02
ORD IDord-bee518b7a7c5416ca27f0f29db853639
Source noteuspto-grants-2007_02