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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637236Generated: October 31, 2026

Sulfuric Acid → N-[5-[[(5-ethyl-2-oxazolyl)methyl]thio]-2-thiazolyl]acetamide

https://huagongshe.com/reaction/1637236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium AcetateHCID 517045—
Reactant[[2-(acetylamino)-5-thiazolyl]thio]-N-(2-oxobutyl)acetamideHCID 10946551—
SolventAcetic AnhydrideHCID 7918—
ProductN-[5-[[(5-ethyl-2-oxazolyl)methyl]thio]-2-thiazolyl]acetamideHCID 532966343%

Reaction Conditions

Temperature57.5 °C

Reaction Steps

To a solution of [[2-(acetylamino)-5-thiazolyl]thio]-N-(2-oxobutyl)acetamide (10.5 g, 34.8 mmol) in acetic anhydride (100 mL) was added conc. sulfuric acid (10 mL). The mixture was stirred at 55-60° C. for 2 h and sodium acetate (15 g, 0.18 mol) was added to the mixture. The mixture was concentrated in vacuo. To the residue was added cold water (100 mL). The precipitated solid was collected, washed with water and dried. It was purified by a flash column chromatography (SiO2 ; methylene chloride: MeOH/100:5) to afford N-[5-[[(5-ethyl-2-oxazolyl)methyl]thio]-2-thiazolyl]acetamide (4.2 g, 43%) as a solid, mp 147-148° C. 1H NMR (CDCl3) δ12.47 (s, 1 H), 7.29 (s, 1 H), 6.61 (s, 1 H), 3.91 (s, 2 H), 2.64 (q, J=7.6 Hz, 2 H), 2.25 (s, 3 H), 1.21 (t, J=7.6 Hz, 3 H) ppm; MS m/e 284 (M+H)+ ;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040321
Source datasetuspto-grants-2000_03
ORD IDord-78028382d36e4f7594de23b8dfd9728c
Source noteuspto-grants-2000_03