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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493237Generated: October 31, 2026

Methylamine → HCID 11722609, compound

https://huagongshe.com/reaction/1493237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantHCID 10442855HCID 10442855—
SolventTolueneHCID 1140—
ProductHCID 11722609HCID 1172260987.6%

Reaction Steps

α-(4-Chlorophenyl)-α-mercaptoacetic acid (5.0 g, 0.025 mol) prepared in Reference Example 4, nicotinaldehyde (2.64 g, 0.025 mol) and 40% aqueous methylamine solution (5.75 g, 0.074 mol) were added to toluene (50 ml) and the mixture was subjected to azeotropic dehydration for 3 hours. After cooled, the mixture was concentrated under reduced pressure and the residue was purified by silica gel chromatography (5% acetone-chloroform) and then recrystallized from ether to obtain 5-(4-chlorophenyl)-3-methyl-2-(3-pyridyl)-thiazolidin-4-one (6.59 g, yield 87.6%). m.p. 100°-101.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021435
Source datasetuspto-grants-1991_06
ORD IDord-3ccd48d8be114e689e17fc2211bd9f99
Source noteuspto-grants-1991_06