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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648590Generated: October 27, 2026

Phosphorus trichloride → 2-Amino-5-(4-pyridyl)-4-[(4-piperonyl-1-piperazinyl)carbonyl]thiazole

https://huagongshe.com/reaction/648590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus trichlorideHCID 24387—
Reactant1-PiperonylpiperazineHCID 94426—
Reactant2-Amino-5-(pyridin-4-yl)-1,3-thiazole-4-carboxylic acidHCID 20144986—
SolventPyridineHCID 1049—
Product2-Amino-5-(4-pyridyl)-4-[(4-piperonyl-1-piperazinyl)carbonyl]thiazoleHCID 2014508119%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 1-piperonylpiperazine (2.72 g) and phosphorus trichloride (0.49 ml) in pyridine (20 ml) was added 2-amino-5-(4-pyridyl)-4-thiazolecarboxylic acid (1.24 g) and the mixture was stirred at 80° C. for 3 hours. The reaction mixture was evaporated in vacuo and the residue was dissolved in a mixture of ethyl acetate and water. The resultant mixture was adjusted to pH 8.0 with saturated aqueous potassium carbonate. The organic extract was dried over magnesium sulfate. The solvent was evaporated in vacuo to give a crystalline residue, which was recrystallized from ethyl acetate to afford 2-amino-5-(4-pyridyl)-4-[(4-piperonyl-1-piperazinyl)carbonyl]thiazole (0.45 g). mp 216°-217° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735957
Source datasetuspto-grants-1988_04
ORD IDord-1fb820e14d0449cf8bd37a69fee45a8d
Source noteuspto-grants-1988_04