Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188137Generated: November 2, 2026

Trifluoroacetic acid → 2-amino-N-(4-p-tolylthiazol-2-yl)thiazole-5-carboxamide

https://huagongshe.com/reaction/1188137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 5-(4-p-tolylthiazol-2-ylcarbamoyl)thiazol-2-ylcarbamateHCID 86643475—
SolventChloroformHCID 6212—
Product2-amino-N-(4-p-tolylthiazol-2-yl)thiazole-5-carboxamideHCID 5940875967%

Reaction Steps

TFA (0.100 mL) was added to a solution of tert-butyl 5-(4-p-tolylthiazol-2-ylcarbamoyl)thiazol-2-ylcarbamate (80 mg, 0.19 mmol) in CHCl3 (1 mL). The resulting solution was stirred at RT overnight. Then the solvents were evaporated and the crude product was dissolved in H2O. After neutralization with NaHCO3 saturated aqueous solution, it was extracted with AcOEt, dried and concentrated. Purification by column chromatography (100% AcOEt) yielded 2-amino-N-(4-p-tolylthiazol-2-yl)thiazole-5-carboxamide (40 mg, 67%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673940B2
Source datasetuspto-grants-2014_03
ORD IDord-25607bf9fc20440aa32123cae8a9dd31
Source noteuspto-grants-2014_03