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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613246Generated: November 1, 2026

Acetic Anhydride → 2-Acetamido-5-(4-nitrobenzyl)-4-propylthiazole

https://huagongshe.com/reaction/1613246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Amino-5-(4-nitrobenzyl)-4-propylthiazoleHCID 19775545—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Product2-Acetamido-5-(4-nitrobenzyl)-4-propylthiazoleHCID 19775558—

Reaction Steps

2 g (7.2 mmol) of 2-amino-5-(4-nitrobenzyl)-4-propylthiazole in 2.5 ml of acetic anhydride, in the presence of 88 mg of 4-dimethylaminopyridine (0.72 mmol), are heated at 80° C. for 1 hour. As the reaction mixture is cooled, the formation of a precipitate is observed. This is filtered off and washed with ether to give 1.6 g of the derivative 2-acetamido-5-(4-nitrobenzyl)-4-propylthiazole, which is pale yellow solid melting at 170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192781
Source datasetuspto-grants-1993_03
ORD IDord-99b661cd7b664243a7b59ff01b96cc47
Source noteuspto-grants-1993_03