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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822821Generated: October 26, 2026

Chloroacetaldehyde → 6-Bromo-N-(2-thiazolyl)pyridin-2-amine

https://huagongshe.com/reaction/1822821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant(6-Bromo-pyridin-2-YL)thioureaHCID 22170428—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Bromo-N-(2-thiazolyl)pyridin-2-amineHCID 2217040196%

Reaction Steps

A suspension of 2-bromo-6-thioureidopyridine (3 g, 12.92 mmol) and chloroacetaldehyde (3.28 mL, 25.85 mmol) in ethanol (27 mL) and water (7 mL) was heated at reflux for 4.75 h. The solution was concentrated in vacuo and the residue was diluted with 1 N aqueous NaOH solution at 0° C., stirred for 10 min, and the pH was then adjusted to 8.5 by addition of 6 N aqueous HCl solution. The precipitate was collected by filtration, washed several times with water and dried in vacuo over P2O5 to obtain the titled compound (3.17 g, 96%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037926B2
Source datasetuspto-grants-2006_05
ORD IDord-f77a4a203f87442f912218cb5445e2e9
Source noteuspto-grants-2006_05