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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494434Generated: October 31, 2026

Triethylamine → HCID 19899254, compound

https://huagongshe.com/reaction/1494434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantHCID 19899242HCID 19899242—
SolventAcetonitrileHCID 6342—
ProductHCID 19899254HCID 19899254—

Reaction Steps

With stirring, 3.2 g of triethylamine are added dropwise at room temperature to 6.0 g of N-[2,6-diethyl-4-(N-formylanilino)phenyl]-N'-tert-butylthiourea and 4.8 g of 2-chloro-1-methylpyridinium iodide in 30 ml of acetonitrile. The reaction mixture is stirred for 1 hour at 70° C. and then concentrated by evaporation at 50° C. on a rotary evaporator. The residue is taken up in 50 ml of hexane and 30 ml of cold water. The hexane phase is separated, washed with water, dried over sodium sulfate and concentrated by evaporation, to give the title compound of formula ##STR21## as a yellowish oil with refractive index nD25 : 1.5840.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026730
Source datasetuspto-grants-1991_06
ORD IDord-976ae3500c7c415a88b8f7f3b9f6b1cc
Source noteuspto-grants-1991_06