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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23356Generated: October 29, 2026

Cyclohexylamine → n-Cyclohexyl-5-(4-nitrophenyl)-1,3-thiazol-2-amine

https://huagongshe.com/reaction/23356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantPotassium thiocyanateHCID 516872—
Reactant2-Bromo-2-(4-nitrophenyl)acetaldehydeHCID 20188849—
SolventMethanolHCID 887—
Productn-Cyclohexyl-5-(4-nitrophenyl)-1,3-thiazol-2-amineHCID 12066444—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of bromo(4-nitrophenyl)acetaldehyde and potassium thiocyanate (1.2 equivalents) in methanol is stirred at room temperature for 1 hour. The cyclohexylamine (1,05 equivalents) is added drop-wise and the mixture is heated under reflux until completion of the reaction (5-12 hours). After cooling to 0° C. the precipitate is filtered off and washed with water. The crude material is purified by usual silica gel chromatography to give the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852720B2
Source datasetuspto-grants-2005_02
ORD IDord-14089d6065474121a1b9c499e0722165
Source noteuspto-grants-2005_02