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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154573Generated: October 30, 2026

2-Aminopyridine → HCID 13089302, compound

https://huagongshe.com/reaction/1154573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantHCID 4164963HCID 4164963—
SolventO-XyleneHCID 7237—
ProductHCID 13089302HCID 1308930267%

Reaction Steps

Into 45 ml of o-xylene, were added 1.5 g of ethyl N-(4-phenyl-2-thiazolyl)carbamate and 4.0 g of 2-aminopyridine. The mixture was stirred for 2.5 hours under refluxing. The reaction solution was allowed to stand for cooling. Deposited crystals were collected by filtration and washed with methyl alcohol. The crystals were then recrystallized from an N,N-dimethylformamide/methyl alcohol mixed solvent to obtain 1.2 g of N-(2-pyridyl)-N'-(4-phenylthiazol-2-yl)urea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490393
Source datasetuspto-grants-1984_12
ORD IDord-e8e18761dcc44cb6aa48ac5c6e401c79
Source noteuspto-grants-1984_12