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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262764Generated: October 26, 2026

Ethanol → 1-(2,6-Dichlorobenzylideneamino)-3-(3-pyridylmethyl)guanidine

https://huagongshe.com/reaction/262764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3-PyridinemethanamineHCID 31018—
ReactantMethyl 3-(2,6-dichlorobenzylidene)thiocarbazimidate hydroiodideHCID 178504060—
SolventWaterHCID 962—
Product1-(2,6-Dichlorobenzylideneamino)-3-(3-pyridylmethyl)guanidineHCID 178512111—

Reaction Steps

A mixture of 5.85 g. of methyl 3-(2,6-dichlorobenzylidene)thiocarbazimidate hydriodide, 3.24 g. of 3-(aminomethyl)pyridine and 25 ml. of absolute ethanol is heated under reflux for 24 hours and diluted while hot with 75 ml. of water. After cooling, an oil separates and crystallizes. The mixture is chilled overnight and the crystals are separated and recrystallized from 100 ml. of 50% aqueous ethanol to give the desired product as pale yellow crystals, m.p. 148°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154947
Source datasetuspto-grants-1979_05
ORD IDord-8c8de0a855b04af48e24d7a007cf8f02
Source noteuspto-grants-1979_05