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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379882Generated: October 30, 2026

4-(6-Acetylaminomethyl-4-chloropyridin-2-yl)-2-(diaminomethyleneamino)thiazole → 4-(6-(Acetamidomethyl)pyridin-2-yl)-2-guanidinothiazole

https://huagongshe.com/reaction/2379882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(6-Acetylaminomethyl-4-chloropyridin-2-yl)-2-(diaminomethyleneamino)thiazoleHCID 18953917—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(6-(Acetamidomethyl)pyridin-2-yl)-2-guanidinothiazoleHCID 1044694090.9%

Reaction Steps

4-(6-Acetylaminomethyl-4-chloropyridin-2-yl)-2-(diaminomethyleneamino)thiazole (160 mg) was hydrogenated over 10% palladium on carbon (50% wt) (50 mg) in methanol (5 ml) at atmospheric pressure of hydrogen for 8 hours at ambient temperature. After the catalyst was removed by filtration, the solvent was evaporated in vacuo and the residue was mixed with water. The solution was adjusted to pH 10 with aqueous potassium carbonate and the free base was extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and evaporated in vacuo to give 4-(6-acetylaminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole (0.13 g). IR (Nujol): 1655, 1590, 1545 cm-1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364871
Source datasetuspto-grants-1994_11
ORD IDord-4cb366dbc6894081889372329930105b
Source noteuspto-grants-1994_11