Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512529Generated: October 25, 2026

4-Methyl-3-nitrobenzoyl chloride → 5-(4-Methyl-3-nitrobenzamido)-2-(naphthalen-2-ylamino)thiazole-4-carboxamide

https://huagongshe.com/reaction/512529

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-3-nitrobenzoyl chlorideHCID 66323—
Reactant5-Amino-2-(naphthalen-2-ylamino)thiazole-4-carboxamideHCID 86703369—
SolventPyridineHCID 1049—
Product5-(4-Methyl-3-nitrobenzamido)-2-(naphthalen-2-ylamino)thiazole-4-carboxamideHCID 8670337166%

Reaction Steps

To a mixture of 5-amino-2-(naphthalen-2-ylamino)thiazole-4-carboxamide (0.2 g, 0.70 mmol) in pyridine (5 mL) was added a solution of 4-methyl-3-nitrobenzoyl chloride in pyridine (3 mL) at 0° C. under nitrogen atmosphere. The mixture was allowed to warm up to rt, and stirred for 16 hrs at rt. The solvent was evaporated, and the crude residue was suspended into EtOAc (20 mL). The resulting solids were collected by filtration and washed with MeOH (2×5 mL) to give 0.21 g (66% yield) of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102637B2
Source datasetuspto-grants-2015_08
ORD IDord-85ebdae6dd3244adadaa17d15c588fcb
Source noteuspto-grants-2015_08