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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030567Generated: November 2, 2026

Dimethylamine → HCID 14999116, compound

https://huagongshe.com/reaction/1030567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantHCID 14999113HCID 14999113—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 14999116HCID 14999116100%

Reaction Conditions

Temperature100 °C

Reaction Steps

A 50% aqueous dimethylamine solution (1.0 ml, 11 mmol) was added to a solution of trans-isomer (128 mg, 0.35 mmol) of 3-(2-chloroethyl)-5-(n-nonyl)-2-(3-pyridyl)thiazolidin-4-one in dimethylsulfoxide (3 ml). The mixture, placed in a sealed tube, was heated at 100° C. for 2 hours. After removal of the solvent by evaporation under reduced pressure, the residue was dissolved in chloroform (30 ml). The solution was washed twice with saturated aqueous NaHCO3 and dried. Removal of the chloroform gave the intended trans-isomer (131 mg, 100% of theoretical) of 3-(2-dimethylaminoethyl)-5-(n-nonyl)-2-(3-pyridyl)thiazolidin-4-one in oily form. IR (CHCl3) [cm-1 ]; 2930, 2860, 1670, 1580, 1355. NMR (δ, CDCl3, ppm); 2.15 (6 H, s), 2.24 (1 H, dt, 12.87 and 5.61 Hz), 2.46 (1 H, ddd, 12.87, 7.20 and 5.94 Hz), 2.69 (1 H, ddd, 14.19, 7.20 and 5.61 Hz), 3.80 (1 H, ddd, 14.19, 5.94 and 5.61 Hz), 4.03 (1 H, ddd, 8.58, 3.96 and 1.98 Hz), 5.86 (1 H, d, 1.98 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106860
Source datasetuspto-grants-1992_04
ORD IDord-d08fdc42f317426c9230da47acd2740b
Source noteuspto-grants-1992_04